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Cat. No. Product name CAS No.
DC10605 Brevianamide F Featured

Brevianamide F , also known as cyclo-(L-Trp-L-Pro), belongs to a class of naturally occurring 2,5-diketopiperazines.

38136-70-8
DC8286 Brexpiprazole(OPC34712) Featured

Brexpiprazole is a novel D2 dopamine partial agonist.

913611-97-9
DC8179 Briciclib(ON 013105,ON 014185) Featured

Briciclib is a small molecule that suppresses cyclin D1 accumulation in cancer cells.

865783-99-9
DC23147 Brigatinib (AP-26113) Featured

Brigatinib (AP-26113, AP26113) is a potent, selective, second generation ALK inhibitor with IC50 of 0.62 nM, exhibits about fivefold greater potency in vitro compared with crizotinib.

1197953-54-0
DC2019 Brivanib (bms-540215) Featured

Brivanib is an ATP-competitive inhibitor against human VEGFR2 and FGFR with IC50 of 25 nM and 148 nM, respectively.

649735-46-6
DC9535 Brivaracetam Featured

Brivaracetam(UCB-34714) is a 4-substituted pyrrolidone butanamide as agent with significant antiepileptic activity; high affinity SV2A ligand and also shows an ability to inhibit Na+ channels.

357336-20-0
DC20180 BRL-50481 Featured

BRL-50481 is a novel and selective inhibitor of phosphodiesterase (PDE) 7 with a Ki value, derived from secondary (Dixon) plots, of 180±10 nM, being at least 200-fold selective for hrPDE7A1 over all other PDEs.

433695-36-4
DC23899 Bromocriptine mesylate Featured

Bromocriptine (CB-154) is a dopamine D2 receptor agonist (Ki=3 nM) and and various serotonin receptors, also inhibits the release of glutamate by reversing the glutamate GLT1 transporter.

22260-51-1
DC8386 Bromodeoxyuridine (BrdU) Featured

Bromodeoxyuridine (BrdU) is a nucleoside analog that competes with thymidine for incorporation into DNA, and used in the detection of proliferating cells.

59-14-3
DC7543 Bromosporine Featured

Bromosporine is a broad spectrum bromodomain inhibitor. Accelerates FRAP recovery of BRD4 and CREBBP in cells at a concentration of 1 μM.

1619994-69-2
DC11038 Bryostatin 1 Featured

Bryostatin 1 (NSC 339555) is a macrocyclic lactone derived from a marine invertebrate, fuctions as an activator of PKC with high binding affinity (Ki=1.35 nM).

83314-01-6
DC9846 BS-181 Featured

BS-181 is a highly selective CDK7 inhibitor with IC50 of 21 nM. ; >40-fold selective for CDK7 than CDK1, 2, 4, 5, 6, or 9.

1092443-52-1
DC8101 BS-181 hydrochloride Featured

BS-181 is a highly selective CDK7 inhibitor with IC50 of 21 nM. ; >40-fold selective for CDK7 than CDK1, 2, 4, 5, 6, or 9.

1397219-81-6
DC8517 BS194 Featured

BS-194 is a selective and potent CDK inhibitor, which inhibits CDK2, CDK1, CDK5, CDK7, and CDK9 with IC50 values of 3, 30, 30, 250, and 90 nM respectively.

1092443-55-4
DC12380 BSJ-03-123 Featured

BSJ-03-123 is a potent, CDK6-selective small-molecule degrader (PROTAC) that uniquely enables rapid pharmacological interrogation of CDK6-dependent functions.

2361493-16-3
DC10460 BT-11 Featured

BT-11 is an orally active and selective LANCL2 modulator.

1912399-75-7
DC10164 BTB-1 Featured

BTB-1 is a small molecule inhibitor of the mitotic motor protein Kif18A.

86030-08-2
DC20199 BTK inhibitor 1;Compound 27 Featured

BTK inhibitor 1 (Compound 27)

2230724-66-8
DC23413 BTRX335140 Featured

BTRX-335140 (CYM-53093, BTRX335140, CYM53093) is a potent, selective, orally active κ opioid receptor (KOR) antagonist with IC50 of 0.8 nM.

2244614-14-8
DC12456 BTT-266 Featured

BTT-266 (BTT266) is a voltage-gated CaV2.2 calcium channel inhibitor that disrupts the CaVα·CaVβ3 protein-protein interaction, directly binds to CaVβ3 with Kd of 3.6 uM.

2413939-89-4
DC23703 BTYNB Featured

BTYNB is a potent and selective inhibitor of IMP1 binding to c-Myc mRNA with IC50 of 5 uM.

304456-62-0
DC9704 Unii-G55ZH52P57 Featured

BTZ043 is a inhibitor of decaprenyl-phosphoribose-epimerase (DprE1), It can display nanomolar bactericidal activity against Mycobacterium tuberculosis in vitro.

1161233-85-7
DCAPI1392 BTZ043 racemate Featured

BTZ043 racemate is a decaprenylphosphoryl-β-D-ribose 2-epimerase (DprE1) inhibitor acting as a new antimycobacterial agent that kill Mycobacterium tuberculosis.

957217-65-1
DC22041 BTZO-1 Featured

BTZO-1 is a cardioprotective agent and Macrophage migration inhibitory factor (MIF) activator, binds to MIF with Kd of 68.6 nM, regulates ARE-mediated gene expression.

99420-15-2
DC6501 Bufalin Featured

Bufalin inhibits steroid receptor coactivator 1 (SRC-1) and SRC-3 at doses as low as 5 nM, promotes the degradation of SRC-3 protein, and inhibits cancer cell growth both in vitro and in vivo.

465-21-4
DCAPI1140 Bumetanide Featured

Bumetanide

28395-03-1
DC11381 Butabindide (oxalate) Featured

Butabindide is a potent inhibitor of cholecystokinin-inactivating peptidase/tripeptidyl peptidase 2 (CCK-inactivating peptidase/TPP-2; Ki = 7 nM).1 It is selective for CCK-inactivating peptidase/TPP-2 over a panel of serine proteases (Kis = >1 μM) as well as CCK receptors (Kis = >0.1 mM).

185213-03-0
DC10693 O-Butyryl timolol Featured

Butyryltimolol is a lipophilic ester prodrug of timolol, a beta adrenergic blocer with antihypertensive and hemodynamic properties.

106351-79-5
DC7563 BV6 Featured

BV6 induced apoptotic and necrotic cell death in monocytes while T-cells, dendritic cells and macrophages were largely protected against BV6-induced cell death.

1001600-56-1
DC8089 BVT 2733(BVT.2733) Featured

BVT 2733 is a selective 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor,protecting osteoblasts against endogenous glucocorticoid induced dysfunction.

376640-41-4
DC8278 BVT-14225 Featured

BVT 14225 is a new selective 11b-HSD1 inhibitor, it belongs to a class of arylsulfonamidothiazoles with in vitro and in vivo antidiabetic effects

376638-65-2
DC21685 BVT-948 Featured

BVT-948 (SPS8I-3) is a noncompetitive, cell-permeable inhibitor of protein tyrosine phosphatases (PTPs) with IC50 of 0.09-1.7 uM. Results show that the effect of BVT948 (BVT.948) is to strengthen the insulin signal and has no effects on the duration of th

39674-97-0
DC12041 BW-A 78U Featured

BW-A 78U is a PDE4 inhibitor with an IC50 of 3 μM.

101155-02-6
DC7675 BX-471(ZK 811752) Featured

BX471 is a potent, selective non-peptide CCR1 antagonist (Ki = 1 nM for human CCR1); exhibits 250-fold selectivity for CCR1 over CCR2, CCR5 and CXCR4.

217645-70-0
DC8808 BX-513 hydrochloride Featured

BX-513 hydrochloride inhibits MIP-1α-induced intracellular calcium mobilization (IC50 = 2.5 μM).

193542-65-3
DC8062 BX517 Featured

BX517 is a novel phosphoinositide-dependent kinase-1 (PDK1) inhibitor.

850717-64-5
DC7092 BX795 Featured

BX795 is a potent and selective dual inhibitor of TBK1/PDK1 with IC50s of 2 nM/6 nM respectively; > 50 fold selectivity over PKA, PKC, c-Kit, GSK3β etc.

702675-74-9
DC7093 BX912 Featured

BX-912 is a selective inhibitor of 3-Phosphoinositide-dependent Kinase-1 (PDK1) with IC50 of 12 nM; >10 fold selectivity over PKA, PKC, C-Kit, EGFR etc.

702674-56-4
DC11219 BXI-72 Featured

BXI-72 (NSC334072) is a potent, selective small molecule Bcl-XL inhibitor that targets the BH3 domain of Bcl-XL (Kd=0.9 nM).

23491-45-4
DC7094 Alpelisib(BYL-719) Featured

BYL719 is a potent and selective PI3Kα inhibitor with IC50 of 5 nM, ;liitle or no effect on PI3Kβ/γ/δ.

1217486-61-7
DC26049 Bz-IEGR-pNA (acetate) Featured

Bz-IEGR-pNA is a colorimetric substrate for Factor Xa.

1325307-57-0
DC11453 Bz-Nle-Lys-Arg-Arg-AMC Featured

Bz-Nle-Lys-Arg-Arg-AMC is a substrate for dengue virus NS2B-NS3 and yellow fever virus NS3 protease.

863975-32-0
DC10864 C188-9 Featured

C188-9 is a potent inhibitor of STAT3 that binds to STAT3 with high affinity (KD=4.7±0.4 nM). C188-9 is well tolerated in mice, shows good oral bioavailability, and is concentrated in tumors.

432001-19-9
DC10937 C25-140 Featured

C25-140 is a specific, first-in-class small molecule inhibitor of the TRAF6-Ubc13 interaction, binds TRAF6, inhibits TRAF6-Ubc13 interaction and TRAF6 activity.

1358099-18-9
DC10276 C29 Featured

C29 is a potential TLR2 inhibitor.

363600-92-4
DC7658 C646 Featured

C646 is an inhibitor for histone acetyltransferase, and inhibits p300 with a Ki of 400 nM. Preferentially selective for p300 versus other acetyltransferases.

328968-36-1
DC9528 C75 (trans) Featured

C75 trans is the trans form of C75; C75 is a potent fatty-acid synthase(FASN) inhibitor with IC50 of 35.4 μM(LNCaP cell Proliferation inhibition).

191282-48-1
DC7697 CA-074-Me Featured

CA-074 Me is a selective and cell-permeable inhibitor of cathepsin B.

147859-80-1
DC10330 PD-1-IN-17 Featured

PD-1-IN-17 has CAS#CAS:1673560-66-1, which is a programmed cell death-1 (PD-1) inhibitor. PD-1-IN-17 was first reported in patent WO2015033301A1, (Compound 4), inhibits 92% splenocyte proliferation at 100 nM. PD-1-IN-17 may be related to CA-170 (AUPM170), which is a potent PD-1 inhibitor and curreently under clinical trials.

1673560-66-1
DC10648 CA4948-Analog Featured

CA4948-Analog is an analog of Emavusertib. It has similar property to CA-4948, which is a potent, and orally active interleukin-1 receptor-associated kinase 4 (IRAK4) inhibitor. It was reported in patent WO 2015104688. Emavusertib, also known as CA-4948 i

1801343-74-7
DC12044 CA-5f Featured

CA-5f is a novel late-stage autophagy inhibitor with potent anti-tumor effect against non-small cell lung cancer.

1370032-19-1
DC26013 Cabotegravir Sodium Featured

Cabotegravir is a potent HIV integrase inhibitor as an oral lead-in tablet and long-acting injectable for the treatment and prevention of HIV infection.

1051375-13-3
DC8180 Cabotegravir(GSK744) Featured

Cabotegravir is a potent HIV integrase inhibitor as an oral lead-in tablet and long-acting injectable for the treatment and prevention of HIV infection.

1051375-10-0
DC9266 Cabozantinib S-malate Featured

Cabozantinib S-malate (XL184, BMS-907351) is a potent VEGFR2 inhibitor with IC50 of 0.035 nM and also inhibits c-Met, Ret, Kit, Flt-1/3/4, Tie2, and AXL with IC50 of 1.3 nM, 4 nM, 4.6 nM, 12 nM/11.3 nM/6 nM, 14.3 nM and 7 nM, respectively.

1140909-48-3
DC10736 CaCC(inh)-A01 Featured

CaCC(inh)-A01 is a non-selective inhibitor of calcium-activated chloride channels (CaCCs) that blocks ATP-stimulated chloride conductance in human salivary gland, intestinal, and bronchial epithelium (mean IC50 = 10 µM).

407587-33-1
DC20856 CAD-031 Featured

CAD-031 (CAD31) is a novel brain penetrant, J147-derivative that has enhanced neurogenic activity over J147 in human neural precursor cells (NPCs).

2071209-49-7
DC10457 Cadazolid (ACT-179811) Featured

Cadazolid (ACT-179811) is a novel fluoroquinolone-oxazolidinone antibiotic and a protein synthesis inhibitor.

1025097-10-2
DC5068 Idelalisib (CAL-101,GS-1101) Featured

CAL-101 is a selective p110δ inhibitor with IC50 of 2.5 nM; shown to have 40- to 300-fold greater selectivity for p110δ thanp110α/β/γ, and 400- to 4000-fold more selectivity to p110δ than C2β, hVPS34, DNA-PK and mTOR.

870281-82-6
DCAPI1559 Calcifediol Featured

Calcifediol is a major circulating metabolite of vitamin D3, acting as a competitive inhibitor with an apparent Ki of 3.9 μM, suppresses PTH secretion and mRNA (ED50=2 nM).

19356-17-3
DCAPI1415 Calcipotriol(Calcipotriene) Featured

Calcipotriol is a synthetic VitD3 analogue with a high affinity for the vitamin D receptor.

112965-21-6
DC10327 Calcitonin salmon Featured

Calcitonin, Salmon is a calcium regulating hormone secreted from mammalian thyroid parafollicular cells and in non-mammalian species from the ultimobranchial gland.

47931-85-1
DCAPI1150 Calcitriol (Rocaltrol) Featured

Calcitriol is the most active metabolite of vitamin D and also a vitamin D receptor (VDR) agonist.

32222-06-3
DC20857 Calhex-231 Featured

Calhex-231 is a potent negative allosteric modulator of CaSR that blocks calcium-mediated activation with IC50 of 0.39 uM.

652973-93-8
DC11275 Calicheamicin Featured

Calicheamicin, also known as Calicheamicin gamma(1,I) or Calichemicin gamma1, is an potent enediyne antitumor antibiotics derived from the bacterium Micromonospora echinospora. Calicheamicin targets DNA and cause strand scission. Calicheamicin binds with DNA in the minor groove, wherein it then undergos a reaction analogous to the Bergman cyclization to generate a diradical species. This diradical, 1,4-didehydrobenzene, then abstracts hydrogen atoms from the deoxyribose (sugar) backbone of DNA, which ultimately leads to strand scission. The specificity of binding of calicheamicin to the minor groove of DNA is due to the aryltetrasaccharide group of the molecule.

108212-75-5
DC20021 Calmidazolium chloride (R 24571) Featured

Calmidazolium chloride (R 24571) is a calmodulin (CaMK) antagonist, antagonizing CaM-dependent phosphodiesterase and calmodulin-induced activation of erythrocyte Ca2+-transporting ATPase with IC50s of 0.15 and 0.35 μM, respectively. Also in anti-cancer re

57265-65-3
DC7095 W-7 hydrochloride Featured

Calmodulin antagonist. Inhibits Ca2+-calmodulin-dependent phosphodiesterase (IC50 = 28 μM) and myosin light chain kinase (IC50 = 51 μM).

61714-27-0
DC7967 calpeptin Featured

calpeptin is Ca2+-dependent protease,calpain inhibitor

117591-20-5
DC8730 Cambendazol Featured

Cambendazol is an antihelmintic that, at a dose of 50 mg/kg/day in mice, eradicates S. ratti adult worms from intestine and S. stercoralis larva from muscle.

26097-80-3
DC10744 Cambinol Featured

Cambinol is a SIRT1 and SIRT2 inhibitor with IC50 values of 56 and 59 μM, respectively.

14513-15-6
DC20859 CAN-508 Featured

CAN-508 is a potent, selective CDK9 inhibitor with IC50 of 0.35 uM (CDK9/cyclin T1), displays >35 fold selectivity over CDK1/2/4/7 (IC50=13.5-70 uM).

140651-18-9
DC3111 Canagliflozin Featured

Canagliflozin is a highly potent and selective SGLT2 inhibitor for CHO-hSGLT2, CHO-rSGLT2 and CHO-mSGLT2 with IC50 of 4.4 nM, 3.7 nM and 2 nM, respectively.

842133-18-0
DC9185 Candesartan cilexetil Featured

Candesartan Cilexetil (TCV-116) is an angiotensin II receptor antagonist used mainly for the treatment of hypertension.

145040-37-5
DC8553 Canertinib Featured

Canertinib (CI-1033) is a pan-ErbB inhibitor for EGFR and ErbB2 with IC50 of 1.5 nM and 9.0 nM, no activity to PDGFR, FGFR, InsR, PKC, or CDK1/2/4. Phase 3. CI-1033 shows excellent potency for irreversible inhibition of erbB2 autophosphorylation in MDA-MB

267243-28-7
DC3138 Canertinib dihydrochloride Featured

Canertinib dihydrochloride is the hydrochloride salt of an orally bio-available quinazoline with potential antineoplastic and radiosensitizing activities.

289499-45-2
DC22425 Cangrelor sodium Featured

Cangrelor (AR-C69931MX) is a potent, selective P2T/P2Y12 receptor antagonist with IC50 of 0.4 nM against ADP-induced aggregation of human platelets.

163706-36-3
DC7005 Cangrelor free acid Featured

Cangrelor is a P2Y12 inhibitor, and was approved in June 2015 as an antiplatelet drug for intravenous application. Cangrelor is a high-affinity, reversible inhibitor of P2Y12 receptors that causes almost complete inhibition of ADP-induced platelet aggrega

163706-06-7
DC4154 Capecitabine Featured

Capecitabine is a tumor-selective fluoropyrimidine carbamate which achieves higher intratumoral 5-FU level with lower toxicity than 5-FU.

154361-50-9
DC7615 Capromorelin Featured

Capromorelin tartrate is a potent ghrelin receptor agonist/growth hormone secretagogue (Ki = 7 nM).

193273-69-7
DC7952 Capasazepine Featured

Capsazepine is a synthetic analogue of the sensory neurone excitotoxin, capsaicin; potent TRPV1 receptor antagonist with IC50 of 562 nM.

138977-28-3
DC9193 Carbamazepine Featured

Carbamazepine, a sodium channel blocker, is an anticonvulsant drug.

298-46-4
DC9095 Carboplatin Featured

Carboplatin is a chemotherapy drug by binding to DNA and interfering with the cell's repair mechanism.

41575-94-4
DC9384 Carboxypeptidase G2 (CPG2) Inhibitor Featured

Carboxypeptidase G2 (CPG2) Inhibitor is a novel Carboxypeptidase G2 (CPG2) Inhibitor, Antitumor agents.

192203-60-4
DC6502 cardamonin Featured

Cardamonin, isolated from the fruits of Alpinia species, is a chalconoid with anti-inflammatory and anti-tumor activity.

19309-14-9
DC8456 Cardiogenol C (hydrochloride) Featured

Cardiogenol C is a diaminopyrimidine that induces cardiomyogenesis in mouse embryonic stem cells.

671225-39-1
DC1002 Carfilzomib (PR-171) Featured

Carfilzomib is an irreversible proteasome inhibitor with an IC50 of 5 nM in ANBL-6 and RPMI 8226 cells,showed potent activity against COVID-19(SARS-COV-2).

868540-17-4
DC8054 Cariprazine (RGH-188) Featured

Cariprazine (RGH-188) is a novel putative antipsychotic drug that exerts partial agonism at dopamine D2/D3 receptors, with preferential binding to D3 receptors, and partial agonism at serotonin 5-HT1A receptors.

839712-12-8
DC24110 CARM1-IN-1 Featured

CARM1-IN-7g is a potent, selective coactivator-associated arginine methyltransferase 1 (CARM1) with IC50 of 8.6 uM, exhibits lower or no activity against a panel of different PRMTs or HKMTs (>80-fold over PRMT1 and SET7).

1020399-49-8
DC8972 Carmustine Featured

Carmustine is a cell-cycle phase nonspecific alkylating antineoplastic agent.

154-93-8
DC8113 Carubicin Featured

Carubicin is an anthracycline antineoplastic antibiotic isolated from the bacterium Actinomadura carminata.

50935-04-1
DC10539 POL1 inhibitor(POL1-IN-1) Featured

CAS 1822358-25-7

1822358-25-7
DC11250 Casein Kinase inhibitor A51 Featured

Casein Kinase inhibitor A51 (CKIα inhibitor A51) is a novel pan-specific CKI (CSNK1) inhibitor (Kd=0.5-20 nM, CKIα Kd=5.3 nM) that co-targets the transcriptional kinases CDK7 and CDK9, with hardly inhibition of CDK8, CDK13, CDK11a, CDK11b, and CDK19; target both CDK7 and CDK9 with low nM Kd values; induces leukemia cell apoptosis at <160 nM, in correlation to the capacity to stabilize p53; shows high and selective sensitivity against leukemic CFUs in colony-forming unit (CFU) assay, without effect on normal hematopoietic CFUs; blocking CKIα together with CDK7 and/or CDK9 synergistically stabilize p53, deprive leukemia cells of survival and proliferation-maintaining SE-driven oncogenes, induce apoptosis, abolishes the expression of MYC, MDM2, and the anti-apoptotic oncogene MCL1; demonstrates therapeutic efficacy with preserved hematopoiesis and leukemia cure potential in AML mouse models.

2079068-74-7
DC8013 CASIN Featured

CASIN is a Cdc42 GTPase inhibitor (IC50 = 2 μM).

425399-05-9
DC22403 Casopitant mesylate Featured

Casopitant (GW679769) is a potent, centrally-acting neurokinin 1 (NK1) receptor antagonist (pKi=9.48) with antidepressant and antiemetic activities.

414910-30-8
DCAPI1497 Cancidas Featured

Caspofungin is a semi-synthetic analogue of pneumocandin B0 with improved water solubility, a significant limitation in the development of the echinocandin class as pharmaceuticals. Caspofungin acts by inhibition of the synthesis of β (1,3)-D-glucan, an e

179463-17-3
DC8482 CAY10415(MSDC-0160) Featured

CAY10415 is a potent, antidiabetic drug of the TZD structural class.

146062-49-9
DC10847 CAY10441(RO1138452) Featured

CAY10441 is a Selective prostacyclin IP receptor antagonist.

221529-58-4
DC10903 CAY10465 Featured

CAY10465 is an analog of resveratrol acting as a potent and selective aryl hydrocarbon receptor agonist, with a Ki of 0.2 nM.

688348-33-6
DC10516 LW6(CAY10585) Featured

CAY10585 prevented HIF-1 transcriptional activity with IC50 values of 2.6 and 0.7 µM, respectively.

934593-90-5
DC10579 CAY 10602 Featured

CAY10602 is a SIRT1 activator.

374922-43-7
DC8036 CAY10603 Featured

CAY10603 is a potent and selective inhibitor of HDAC6 with IC50 of 2 pM, as compared with 271, 252, 0.42, 6851, and 90.7 nM for HDAC1, 2, 3, 8, and 10, respectively.

1045792-66-2
DC7738 CAY10683(Santacruzamate A) Featured

CAY10683 is a potent and selective HDAC inhibitor with IC50 of 119 pM for HDAC2, >3600-fold selectivity over other HDACs.

1477949-42-0
DC4160 CB-03-01 Featured

CB-03-01 is a steroidal ester, androgen antagonist derived from 11-deoxycortisone, which tightly mimics the profile of an ideal anti-androgen for topical use.

19608-29-8
DC8840 CB-5083 Featured

CB-5083 is a novel first in class, potent orally bio-available p97 inhibitor that disrupts cellular protein homeostasis and demonstrates anti-tumor activity in solid and hematological models .

1542705-92-9
DC20052 CB-6644 Featured

CB-6644 is a selective inhibitor of RUVBL1/2 complex with anti-cancer activity. CB-6644 blocks the ATPase activity of RUVBL1/2 with an IC50 of 15 nM.

2316817-88-4
DC10449 CB7921220 Featured

CB7921220 is an inhibitor of Adenylyl Cyclase isoform-1 (AC1) and isoform-6 (AC6).

115453-99-1
DC8042 CB-839(Telaglenastat) Featured

CB-839 is a potent, selective, reversible and orally bioavailable inhibitor of human glutaminase.

1439399-58-2
DC10617 CBL0137 Featured

CBL0137 is a metabolically stable curaxin that activates p53 with an EC50 value of 0.37 µM and inhibits NF-κB with an EC50 of 0.47 µM.

1197996-80-7
DC8377 CC-115 Featured

CC-115 is a dual inhibitor of DNA-dependent protein kinase (DNA-PK) and mammalian target of rapamycin (mTOR), with potential antineoplastic activity.

1228013-15-7
DC10146 CC-122(Avadomide) Featured

CC-122 is a novel agent for DLBCL with antitumor and immunomodulatory activity.CC-122 binds CRBN and degrades Aiolos and Ikaros resulting in a mimicry of IFN signaling and apoptosis in DLBCL.

1015474-32-4
DC8497 CC-223 Featured

CC-223 is a potent mTOR kinase inhibitor (IC50=16 nM), with >150-fold sensitivity over the related lipid kinase PI3Kα (IC50=4 μM).

1228013-30-6
DC7096 CC-401 Featured

CC-401 is a second generation ATP-competitive anthrapyrazolone c-Jun N terminal kinase (JNK) inhibitor with potential antineoplastic activity.

1438391-30-0
DC20866 CC-671 Featured

CC-671 is a potent, selective, dual TTK (Mps1)/CLK2 inhibitor with IC50 of 5/3 nM, respectively.

1618658-88-0
DC11588 CC-885 Featured

CC-885 (CC 885, CC885) is a novel E3 ligase cereblon (CRBN) modulator with potent anti-tumour activity mediated through the degradation of GSPT1.

1010100-07-8
DC12590 CCB 02 Featured

CCB02 (CCB 02) is a specific small molecule inhibitor of CPAP-tubulin interaction with IC50 of 0.689 uM in AlphaScreen assay, selectively binds at the CPAP binding site of tubulin.

2100864-57-9
DC7319 CCDC(TGR5-Receptor-Agonist) Featured

CCDC is a otent, selective TGR5 G-protein coupled receptor agonist (pEC50 = 6.8).

1197300-24-5
DC9757 CCF642 Featured

CCF642 is a novel protein disulfide isomerases (PDI) inhibitor.

346640-08-2
DC7979 CCG1423 Featured

CCG-1423 is a novel inhibitor of RhoA/C-mediated gene transcription that is capable of inhibiting invasion of PC-3 prostate cancer cells in a Matrigel model of metastasis.

285986-88-1
DC10535 CCG-203971 Featured

CCG-203971 is an inhibitor of SRE activation in the prostate cancer cell line PC-3 (IC50 = 6.4 μM), with 87% inhibition of SRE activation achieved at 100 μM.

1443437-74-8
DC11302 CCG215022 Featured

CCG215022 is a G protein-coupled receptor kinases (GRKs) inhibitor with IC50s of 0.15±0.07 μM, 0.38±0.06 μM and 3.9±1 μM for GRK2, GRK5 and GRK1, respectively.

1813527-81-9
DC22819 CCG-50014 Featured

CCG-50014 is the most potent against the regulator of G-protein signaling protein type 4 (RGS4) (IC50 =30 nM) and is >20-fold selective for RGS4 over other RGS proteins. CCG-50014 binds covalently to the RGS, forming an adduct on two cysteine residues located in an allosteric regulatory site. CCG50014, reduces nociceptive responses and enhances opioid-mediated analgesic effects in the mouse formalin test.

883050-24-6
DC26030 CCMI Featured

CCMI is a positive allosteric modulator of α7 neuronal nicotinic acetylcholine receptors (nAChR).

917837-54-8
DC12302 CCR2 antagonist 3 Featured

CCR2 antagonist 3 is a chemokine receptor 2 (CCR2) antagonist.

1380100-86-6
DC7803 CCT007093 Featured

CCT007093 is a potent PPM1D (WIP1) inhibitor with IC50 of 8.4 μM.

176957-55-4
DC10005 CCT196969 Featured

CCT196969 is a novel orally available, pan-RAF inhibitor with anti-SRC activity.

1163719-56-9
DC10911 CCT241736 Featured

CCT241736 is a novel, orally bioavailable Dual FLT3-Aurora Kinase Inhibitor.

1402709-93-6
DC8324 CCT244747 Featured

CCT244747 represents the first structural disclosure of a highly selective, orally active CHK1 inhibitor and warrants further evaluation alone or combined with genotoxic anticancer therapies.

1404095-34-6
DC10498 CCT251236 Featured

CCT251236 is an orally available pirin ligand from a heat shock transcription factor 1 (hsf1) phenotypic screen with an IC50 of 19 nM for inhibition of HSF1-mediated HSP72 induction.

1693731-40-6
DC9968 CCT251545 Featured

CCT251545 is an orally bioavailable and potent inhibitor of WNT signaling with IC50 value of 5 nM.

1661839-45-7
DC11679 CCT-367766 Featured

CCT367766 is a potent and the third generation heterobifunctional and PROTAC-based pirin targeting protein degradation probe (PDP), depletes pirin protein expression at low concentration. CCT367766 exhibits a moderate affinity for the CRBN-DDB1 complex with an IC50 value of 490 nM. CCT367766 reveals a good affinity for the recombinant pirin and CRBN with Kd values of 55 nM and 120 nM, respectively. CCT367766 provides a potential chemical tool to study a largely unexplored protein[1].

2229856-58-8
DC20332 CD38 inhibitor 78c Featured

CD38 inhibitor 78c is a potent, specific, reversible CD38 inhibitor with Ki of 14.5 nM for recombinant human CD38.

1700637-55-3
DC10491 CD437 Featured

CD437 is a synthetic retinoid that is an RARγ-selective agonist. It displays RARγ-dependent and -independent effects on differentiation and apoptosis.

125316-60-1
DC10909 BN82002 Featured

CDC25 Phosphatase Inhibitor I, BN82002, is a cell-permeable ortho-hydroxybenzylamino compound that has been reported to display antitumor properties.

396073-89-5
DC8361 CDDO(Bardoxolone; RTA 401) Featured

CDDO is a synthetic oleanane triterpenoid that blocks the cellular synthesis of inducible nitric oxide synthase and inducible COX-2 in INF-γ-activated mouse macrophages with an IC50 value of 0.4 nM.

218600-44-3
DC12026 CDDO-2P-Imidazolide Featured

CDDO-2P-Im is a new analogue of CDDO-Imidazolid,showing better bioactive than CDDO-Imidazolid.

1883650-96-1
DC12027 CDDO-3P-Imidazolide Featured

CDDO-3P-Im is a new analogue of CDDO-Imidazolid,showing better bioactive than CDDO-Imidazolid.

1883650-95-0
DC12025 CDDO imidazolide Featured

CDDO-imidazolide is a potent inducer of heme oxygenase-1 and Nrf2/ARE signaling,with potent antiproliferative, differentiating, and anti-inflammatory activities.

443104-02-7
DC9277 C-DIM12 Featured

C-DIM12 is a novel synthetic activator of Nurr1.

178946-89-9
DC10792 DIM-C-pPhOCH3(C-DIM5) Featured

C-DIM5 is a Nur77 agonist. Activation of the orphan nuclear receptor Nur77 by C-DIM5 is associated with decreased cancer cell survival,

33985-68-1
DC20334 CDK2 inhibitor 73 Featured

CDK2 inhibitor 73 is a potent, selective CDK2 inhibitor with IC50 of 44 nM for CDK2/cyclin A, displays 2,000-fold selectivity over CDK1/cyclin B (IC50=86 uM)..

2079895-42-2
DC20335 CDK9-IN-8 Featured

CDK9-IN-8 is a highly potent, selective CDK9 inhibitor with IC50 of 12 nM, shows good selectivity in CDKs kinase profiling assay against CDK kinases and cell proliferation inhibition.

2105956-51-0
DC23138 CDK-I73 Featured

CDKI-73 is a potent CDK9 inhibitor with Ki of 4 nM, shows cytotoxicity against a broad CLL samples with mean LD50 of 80 nM.

1421693-22-2
DC9390 CDK-IN-2 Featured

CDK-IN-2 is a potent and sepecific CDK inhibitor.

1269815-17-9
DC11393 CDM-NAG Featured

CDM-NAG is a useful tool compound to deliver the siRNA.

1299292-01-5
DC10948 CDN1163 Featured

CDN1163 (CDN-1163) is a small molecule, allosteric activator of SERCA2, dose-dependently increases the Vmax of SERCA2 Ca2+-ATPase activity in ER microsomes; increases Ca2+-ATPase activity and significantly enhances Ca2+ uptake into the ER, attenuates H2O2-stimulated cell death in HEK cells; improves glucose homeostasis and metabolic parameters, increases glucose tolerance in ob/ob mice; CDN1163 reduces lipid accumulation and decreases lipogenesis in obese mice livers.

892711-75-0
DC23463 CDPPB Featured

CDPPB is a potent, selective, brain penetrant positive allosteric modulator of mGlu5 receptor with EC50 of 10 nM and 20 nM for human and rat mGluR5, respectively.

781652-57-1
DC20336 CE3F4 Featured

CE3F4 is a potent, noncompetitive EPAC1 inhibitor that blocks EPAC1-induced Rap1 activation both in cell-free systems and in intact cells and did not influence protein kinase A holoenzyme activity.

143703-25-7
DC20987 Cedazuridine Featured

Cedazuridine (E7727) is a novel cytidine deaminase inhibitor, and a componet of ASTX727 for treatment of hematologic malignancies..

1141397-80-9
DC3170 Cediranib Featured

Cediranib (AZD2171) is a highly potent VEGFR2 inhibitor with IC50 of 0.5 nM, also inhibits Flt1/4 with IC50 of 5 nM/≤3 nM.

288383-20-0
DC8067 Cefozopran Featured

Cefozopran (SCE-2787) is a new parenteral cephalosporin, against experimental infections in mice.

113359-04-9
DCAPI1155 Celastrol Featured

Celastrol is a potent proteasome inhibitor for the chymotrypsin-like activity of a purified 20S proteasome with IC50 of 2.5 μM.

34157-83-0
DCAPI1491 Celecoxib Featured

Celecoxib is a selective Cox-2 inhibitor (IC50 of 40 nM). Celecoxib shows low sensitivity against Cox-1 (IC50 of 15 μM). Celecoxib shows an anti-proliferative effect on nasopharyngeal carcinoma (NPC) cell lines including HNE1 (IC50of 32.86 μM) and CNE1-LM

169590-42-5
DC7568 Z-DEVD-FMK Featured

Cell-permeable, irreversible inhibitor of caspase-3/CPP32; inhibits tumor cell apoptosis. Neuroprotective in rat hippocampus following seizures in vivo.

210344-95-9
DC9923 CeMMEC1 Featured

CeMMEC1 is a novel potent inhibitor of the second bromodomain of TAF1, binding neither the first nor the second bromodomain of BRD4.

440662-09-9
DC10316 Cenicriviroc Featured

Cenicriviroc is an orally active, dual CCR2/CCR5 antagonist, and displays potent anti-inflammatory and aninfective activity.

497223-25-3
DC10010 Centrinone Featured

Centrinone is a selective and reversible inhibitor of polo-like kinase 4 (Plk4), a serine-threonine protein kinase that initiates centriole/centrosome assembly.

1798871-30-3
DC8138 CEP-28122 Featured

CEP-28122 is a highly potent and selective orally active inhibitor of anaplastic lymphoma kinase with antitumor activity in experimental models of human cancers.

1022958-60-6
DC8196 CEP-32496 Featured

CEP-32496 is a highly potent inhibitor of BRAF(V600E/WT) and c-Raf with Kd of 14 nM/36 nM and 39 nM, also potent to Abl-1, c-Kit, Ret, PDGFRβ and VEGFR2, respectively; insignificant affinity for MEK-1, MEK-2, ERK-1 and ERK-2.

1188910-76-0
DC7099 CEP33779 Featured

CEP33779(< 3 μM) inhibits phosphorylation of downstream target signal transducer and activator of transcription 5(pSTAT5) of JAK2 in a concentration dependent manner in HEL92 cells.

1257704-57-6
DC8009 CEP-37440 Featured

CEP-37440 is a novel potent and selective Dual FAK/ALK inhibitor with IC50 s of 2.3 nM (FAK) and 120 nM(ALK cellular IC50 in 75% human plasma).

1391712-60-9
DC10337 CEP-40783 Featured

CEP-40783 is a potent, selective and orally available inhibitor of AXL and c-Met with IC50 values of 7 nM and 12 nM, respectively.

1437321-24-8
DC7347 Cephalosporin C Na salt Featured

Cephalosporin C Na salt is used to study the effect of transpeptidase expression, binding, and inhibition on bacterial cell wall mucopeptide synthesis.

74970-31-3
DC7346 Cephalosporin C zinc salt Featured

Cephalosporin C zinc salt is used to study the effect of transpeptidase expression, binding, and inhibition on bacterial cell wall mucopeptide synthesis.

59143-60-1
DC9649 Cephalotaxlen Featured

Cephalotaxine is an antiviral as well as antitumor agent.

24316-19-6
DC9765 CERC-501(LY-2456302,Aticaprant) Featured

CERC-501(LY-2456302) is a potent, selective antagonist of the kappa opioid receptor (KOR) (Ki = 0.81 nM vs. 24.0 nM and 155 nM for the μ-opioid receptor (MOR) and δ-opioid receptor (DOR), respectively.

1174130-61-0
DC7814 Cerdulatinib(PRT-062070; PRT2070) Featured

Cerdulatinib(PRT-062070; PRT2070) is an novel oral dual Syk/JAK inhibitor.

1198300-79-6
DC9500 Cevimeline (hydrochloride hemihydrate) Featured

Cevimeline hydrochloride hemihydrate, a novel muscarinic receptor agonist, is a candidate therapeutic drug for xerostomia in Sjogren's syndrome.

153504-70-2
DC10440 Namodenoson (CF-102) Featured

CF-102(2-Cl-IB-MECA) is a selective A3 adenosine receptor agonist (Ki = 0.33 nM). Displays 2500- and 1400-fold selectivity over A1 and A2A receptors respectively. target: A3 adenosine receptor agonist;

163042-96-4
DC10069 CFI-400437 Featured

CFI-400437 is potent against PLK4 (IC50 = 0.6 nM) and selective against other members of the PLK family (>10 uM).

1247000-76-5
DC22809 c-FMS-IN-8 Featured

c-FMS-IN-8 is a potent, selective c-FMS kinase inhibitor with IC50 of 0.8 nM, shows activity in collagen-induced model of arthritis in mice..

885704-21-2
DC7039 CFTR Inhibitor II Featured

CFTR Inhibitor II is a cell-permeable glycinyl hydrazone compound that acts as a potent, selective and reversible open-channel blocker of CFTR with intermediate speed (< 1 min; 95% inhibition at 50 µM; Ki = 4.3 µM in CFTR-expressing FRT cells.

328541-79-3
DC12580 CG-806 Featured

CG-806 (CG806, CG'806) is a novel potent, pan-FLT3/BTK multi-kinase inhibitor with impressive inhibition of leukemic cell proliferation with IC50 at sub-nanomolar or low nanomolar levels.

1370466-81-1
DC7380 CGI-1746 Featured

CGI1746 is a small-molecule Btk inhibitor chemotype with a new binding mode that stabilizes an inactive nonphosphorylated enzyme conformation.

910232-84-7
DC7101 CGK733 Featured

CGK 733 is a potent and selective inhibitor of ATM/ATR with IC50 of ~200 nM.

905973-89-9
DC10843 CGP 52432 Featured

CGP 52432 is a potent, selective GABAB receptor antagonist (IC50 = 85 nM).

139667-74-6
DC7381 CGP-57380 Featured

CGP 57380 is a cell-permeable pyrazolo-pyrimidine compound that acts as a selective inhibitor of Mnk1 (IC50 = 2.2 μM) with no inhibitory activity against p38, JNK1, ERK1/2, PKC, or Src-like kinases.

522629-08-9
DC10722 CGP-71683A Featured

CGP 71683A is a potent and highly selective non-peptide antagonist of the NPY Y(5) receptor in the study of obesity.

192322-50-2
DC23919 CGP-42112 Featured

CGP-42112 (CGP42112A) is a highly potent, selective Angiotensin-II subtype 2 receptor(AT2 receptor) agonist with Ki of 0.24 nM.

127060-75-7
DC8471 CGS 21680 hydrochloride Featured

CGS 21680 hydrochloride is an A2A adenosine receptor agonist (Ki = 27 nM).

124431-80-7
DC7939 CH-223191 Featured

CH-223191 is a ligand-selective antagonist of the Ah (Dioxin) receptor.

301326-22-7
DC7102 CH5132799 Featured

CH5132799 selectively inhibits class I PI3Ks, such as PI3Kα, PI3Kβ, PI3Kδ, and PI3Kγ with IC50 values of 0.014, 0.12, 0.50, and 0.36 uM, respectively; shows less inhibition of class II PI3Ks, class III PI3ks, and mTOR.

1007207-67-1
DC8418 CH5183284 (Debio-1347) Featured

CH5183284 is a selective and orally available FGFR inhibitor with IC50 of 9.3 nM, 7.6 nM, 22 nM, and 290 nM for FGFR1, FGFR2, FGFR3, and FGFR4, respectively. Phase 1.

1265229-25-1
DC7383 CH5424802(Alectinib) Featured

CH5424802(AF 802; Alectinib) is a potent ALK inhibitor with IC50 of 1.9 nM, sensitive to L1196M mutation.

1256580-46-7
DC8728 CH5424802(Alectinib HCl) Featured

CH5424802(AF 802; Alectinib) is a potent ALK inhibitor with IC50 of 1.9 nM, sensitive to L1196M mutation.

1256589-74-8
DC22054 CH5447240 Featured

CH5447240 is a novel potent, selective, orally active hPTHR1 agonist with EC20 of 3.0 nM and EC50 of 12 nM.

1253919-92-4
DC12415 CH7057288 Featured

CH7057288 (CH-7057288) is a novel potent and selective pan-TRK inhibitor with IC50 of 1.1/7.8/5.1 nM for TRKA/TRKB/TRKC, respectively.

2095616-82-1
DC23101 Chelerythrine chloride Featured

Chelerythrine is a potent, cell permeable inhibitor of protein kinase C (IC50 = 660 nM) that does not inhibit tyrosine protein kinases, cAMP-dependent protein kinase, or calcium/calmodulin-dependent protein kinase.

3895-92-9
DC20266 Chelerythrine Featured

Chelerythrine is a well-known protein kinase C inhibitor, can inhibit telomerase activity, it also can block the human P2X 7 receptor.

34316-15-9
DC20100 Chelidonic acid Featured

Chelidonic acid is a component of Chelidonium majus L., used as a mild analgesic, an antimicrobial, an acentral nervous system sedative. Chelidonic acid also shows anti-inflammatory activity. Chelidonic acid has potential to inhibit IL-6 production by blo

99-32-1
DC21405 Chetomin Featured

Chetomin (NSC 289491) is a natural product isolated from Chaetomium species which shows antibacterial and antifungal properties, disrupts the interaction of HIF-1α/p300 at low nanomolar concentrations, strongly increases retinal pigment epithelial cells d

1403-36-7
DC7978 Tucidinostat(Chidamide) Featured

Chidamide is a class I HDAC inhibitor with IC50s of 95/160/67/733 nM for HDAC1/2/3/8; also inhibits HDAC10/11(IC50=78/432 nM); no inhibition on HDAC4/5/7/9/6(IC50>30 uM).

743420-02-2
DC9292 CHIR-090 Featured

CHIR-090 is a potent LpxC inhibitor, displays two-step time-dependent inhibition and kills a wide range of Gram-negative pathogens as effectively as ciprofloxacin or tobramycin.

728865-23-4
DC7384 CHIR-98014 Featured

CHIR-98014 is a potent GSK-3α/β inhibitor with IC50 of 0.65 nM/0.58 nM, with the ability to distinguish GSK-3 from its closest homologs Cdc2 and ERK2.

252935-94-7
DC9703 CHIR-99021 HCl Featured

CHIR-99021 HCl is a glycogen synthase kinase 3 beta inhibitor that has antiproliferative activity in vitro and in vivo.

1797989-42-4
DC1023 CHIR-99021 (CT99021) Featured

CHIR-99021 is a glycogen synthase kinase 3 beta inhibitor that has antiproliferative activity in vitro and in vivo.

252917-06-9
DC9082 Chlorpromazine HCl Featured

Chlorpromazine Hydrochloride is a dopamine and potassium channel inhibitor used as the prototypical phenothiazine antipsychotic drug.

69-09-0
DC10467 CHMFL-BMX-078 Featured

CHMFL-BMX-078 is a highly potent and selective type II irreversible BMX kinase inhibitor with an IC50 of 11 nM.

1808288-51-8
DC8116 Tosedostat (CHR2797) Featured

CHR-2797 is an aminopeptidase inhibitor, with IC50 values of 100 nM for LAP3 (LAP), 150 nM for PSAP (PuSA) and 220 nM for CD13 (Aminopeptidase N).

238750-77-1
DC9460 CHR-6494 Featured

CHR-6494 is a potent and selective Haspin (Haploid Germ Cell-Specific Nuclear Protein Kinase) inhibitor that blocks H3T3ph phosphorylation.

1333377-65-3
DC8139 GMX1778(CHS-828) Featured

CHS-828 is a pyridyl cyanoguanidine anti-tumor agent that has been identified as a competitive inhibitor of Nampt as well as an inhibitor of NF-κB pathway activity.

200484-11-3
DC2088 CI-1040 (PD184352) Featured

CI-1040 (PD 184352) is an ATP non-competitive MEK1/2 inhibitor with IC50 of 17 nM.

212631-79-3
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