Home > Inhibitors & Agonists
Cat. No. Product name CAS No.
DCC4796 Smcy 5.5

Fluorogenic fluorescent probe for imaging lipid droplets; suitable for use with two-photon microscopy

2417507-09-4
DCC4797 Smdc818909

Novel Allosteric Inhibitor of p97

1147823-21-9
DCC4798 Smer10

Novel enhancer of the clearance of mutant aggregate-prone proteins by autophagy in mammalian cell models of Huntington's and Parkinson's disease, independent of rapamycin

221238-83-1
DCC4799 S-mgb-234 Bis-tfa Salt

Novel strathclyde minor groove binder (S-MGB), curing animal African trypanosomiasis (AAT)

1970223-54-1
DCC4800 smip001

Novel enhancer of the cyclin-dependent kinase (CDK) inhibitor p27(Kip)

397872-93-4
DCC4801 Smip2.1

Novel TLR2 agonist, promoting cross-presentation by mouse and human antigen presenting cells

DCC4802 Smk-17

Novel highly hydrophilic and non-ATP-competitive MEK1/2 inhibitor

765958-29-0
DCC4803 Sml-10-70-1

Selective, direct-acting covalent inhibitor of the K-Ras G12C mutant relative to wild-type Ras

1536470-98-0
DCC4804 Sml-8-73-1

Novel Active Site Inhibitor of Oncogenic K-Ras G12C

DCC4805 Smn2-stablizer-27

Novel Stablizer of Survival of Motor Neuron 2 (SMN2) , Post-Translationally Stablizing SMN Protein for the Treatment of Spinal Muscular Atrophy (SMA)

DCC4806 Smn-c5

Novel specific splicing enhancer, targeting RNA for a specific splicing correction, recognizing the interface between U1 snRNP and the SMN2 E7 5ʹ SS, promoting the U1-C zinc finger RNA duplex binding activity

DCC4807 Smt022357

Second-generation modulator of utrophin, increasing utrophin expression in skeletal, respiratory and cardiac muscles

DCC4808 Smtp-7

Novel dual inhibitor of thrombolysis and soluble epoxide hydrolase

273379-50-9
DCC4809 Smurf1 Inhibitor 1

Novel Smurf1 inhibitor, promoting bone formation in mouse models of distinctive age-related osteoporosis

136068-42-3
DCC4810 Smu-z1

Novel potent TLR1/2 Specific Agonist, Suppressing Leukemia Cancer Cell Growth by Stimulating Cytotoxic T Lymphocytes

DCC4811 Sn16713

Selective ligand of GC-rich sequences in DNA

88476-68-0
DCC4812 Sn-28049

Novel potent DNA-binding topoisomerase II-directed antitumor agent.

492472-30-7
DCC4813 Sn34037

Novel specific inhibitor of Aldo-keto reductase 1C3 (AKR1C3, EC 1.1.1.188)

1548116-54-6
DCC4814 Sn-38 Prodrug 3c

Novel Bioorthogonal Prodrug of SN-38 with Fast Reaction Kinetics and High Releasing Efficiency In Vivo

DCC4815 Snap-398299

Potent and selective GAL3 antagonist

903878-06-8
DCC4816 Snap-5089

Highly selective alpha1A-adrenoceptor antagonist

157066-77-8
DCC4817 Sniper(abl)-38

Specific and Nongenetic IAP-dependent Protein Eraser (SNIPER), acting as a protein degradation inducer of oncogenic BCR-ABL protein

DCC4818 Sniper(brd4)-1

Specific and Nongenetic Inhibitor of Apoptosis Protein (IAP)-dependent Protein Eraser (SNIPER), acting as a a protein degradation inducer of bromodomain-containing protein 4 (BRD4)

DCC4819 Sniper(ch6)

Novel fused proteins degrader of the His-tagged CRABP-II and Smad2 in cells

DCC4820 Sniper(crabp)-11

Novel potent degrader of the mitochondrial CRABP-II protein

1384275-50-6
DCC4821 Sniper(er)-87

Novel potent and selective degrader of the ERα protein

2222354-91-6
DCC4822 Sniper(pde4)-9

Specific and Nongenetic Inhibitor of Apoptosis Protein (IAP)-dependent Protein Eraser (SNIPER), acting as a a protein degradation inducer of phosphodiesterase-4 (PDE4)

DCC4823 Snri-h05

Novel potent serotonin and noradrenaline reuptake inhibitor (SNRI) with moderate 5-HT2A antagonist activity for anti-depression

DCC4824 sns-oh

Inducer of apoptosis in neuroblastoma cells through inhibition of AKT signaling pathway

1354834-09-5
DCC4825 Snu-bp

Novel agonist of PPAR-gamma, inhibiting lipopolysaccharide (LPS)-induced NO production and pro-inflammatory cytokines, potentiating interleukin-4-induced arginase-1 expression, promoting microglial polarization toward to an M2 anti-inflammatory phenotype

1621513-98-1
DCC4826 Snx2-1-108

Highly selective inhibitor of CDK8 and its isoform CDK19

1366002-73-4
DCC4827 So1989

Novel macrophage modulator, inhibiting inflammation and M1 polarization of macrophages, restoring the balance between M1-polarized and M2-polarized macrophages in high fat diets (HFD)-induced obese mice resulting in the improvement of adipose inflammation

DCC4828 soblidotin

Inhibitor of tubulin polymerization, resulting in cell cycle arrest and induction of apoptosis

149606-27-9
DCC4829 Sobuzoxane

Orally available active prodrug of ICRF-154, interferring with topoisomerase II activity prior to the formation of intermediate cleavable DNA-enzyme complexes during the catalytic cycle resulting in tumor cell growth inhibition

98631-95-9
DCC4830 Sod1-derlin-1 Inhibitor 56-20

Novel potent inhibitor of SOD1-Derlin-1 interaction

840461-03-2
DCC4831 Sod1-derlin-1 Inhibitor 56-26

Novel potent inhibitor of SOD1-Derlin-1 interaction

489402-79-1
DCC4832 Sodelglitazar

PPARdelta receptor agonist

447406-78-2
DCC4833 Sodium Dehydrocholate

Hepatoprotective and choleretic agent

145-41-5
DCC4834 Sodium Oxybate

Narcolepsy agent, being used to treat catalepse and daytime sleepiness in patients with narcolepsy

502-85-2
DCC4835 Solanidine

Natural tumor antagonistic steroidal alkaloid, inducing typical cellular apoptotic hallmarks and cell cycle blockage at S-G2/M phase, activating nuclear import of DFF-40 mediated nucleosomal disruption and cell demise

80-78-4
DCC4836 Solimastat

Novel oral, broad-spectrum matrix metalloproteinase inhibitor (MMPI), being >10-fold more active than marimastat in inhibiting the processing of cell-bound TNF-alpha

226072-63-5
DCC4837 Somapacitan

Novel long-acting, reversible albumin-binding growth hormone (GH) derivative for treatment of growth hormone dificiency

1338578-34-9
DCC4838 Somatoprim

Unique somatostatin receptor subtypes 2-, 4- and 5-selective analogue, effectively reducing GH secretion in human GH-secreting pituitary adenomas even in Octreotide non-responsive tumours.

252845-37-7
DCC4839 Somcl-668

Novel potent and selective allosteric modulator of sigma-1 receptor

DCC4840 Somcl-863

Novel, selective and orally bioavailable c-Met inhibitor, exhibiting antitumor activity both in vitro and in vivo

1452310-87-0
DCC4841 Sonedenoson

A2A adenosine receptor agonist

131865-88-8
DCC4842 Sophoradin

Natural analgesic, antipyretic, anti-inflammatory, and anti-tumor agent

23057-54-7
DCC4843 Sophorafavanone A

Inhibitor of constitutive and inducible STAT3 activation through the activation of SHP-2 tyrosine phosphatase

87893-18-3
DCC4844 Sophoraflavanone B

Natural inhibitor of the Kv1.3 channels in a concentration-dependent manner

68682-02-0
DCC4845 soraphinol A

Human norepinephrine transporter blocker

1006373-58-5
DCC4846 sori-20041

DAT modulator, being unique in affecting substrate uptake without impacting efflux

488082-05-9
DCC4847 sori-9804

Novel partial inhibitor of amphetamine-induced dopamine release

434326-29-1
DCC4848 Sortin3 Maleate

Sorting inhibitor, blocking Vps16 function, one protein in the class C tethering complex, and increasing aflatoxin synthesis and export

DCC4849 Spam (signal Peptide-based Affinity Maturated Ligand)

Novel Programmed Death Ligand 1 (PD-L1) Binding Peptide (a Peptide Ligand for PD-L1)

DCC4850 spb03924

Novel telomerase inhibitor

263766-82-1
DCC4851 SPB08007

0

DCC4852 Spd-2-am

Novel photo-controllable hydrogen sulfide donor applicable in live cells

DCC4853 Spectinamide-1599

Novel anti-tuberculosis agent against intracellular Mycobacterium tuberculosis

DCC4854 Spectinomycin Dihydrochloride

Antibiotic, binding to the bacterial 30S ribosomal subunit, interfering with the initiation of protein synthesis and with proper protein elongation and leading to bacterial cell death

21736-83-4
DCC4855 Spi-1865

Novel gamma-secretase modulator

DCC4856 Spirohydantoin-21

Novel selective orally bioavailable inhibitor of p300/CBP histone acetyltransferase

DCC4857 Spirooxindole 1a

Novel p53 Stabilizer for Brain Cell Differentiation

DCC4858 Spiroxamine

Sterol Biosynthesis Inhibitor, Fungicide

118134-30-8
DCC4859 Spla2 Inhibitor Pyr-1

Novel potent sPLA2 inhibitor, selectively targeting hGIIA and hGIID

DCC4860 Spmtrien

Novel isosteric charge-deficient spermine analogue

DCC4861 spongiacidin C

USP7 inhibitor from the marine sponge Stylissa massa

193202-57-2
DCC4862 Spongosine

Pivotal intercellular signal transmitter

24723-77-1
DCC4863 Spop-in-6lc

Novel SPOP inhibitor, suppressing the viability and inhibiting the colony formation of ccRCC cell lines driven by cytoplasmic SPOP

2136270-56-7
DCC4864 Spt-in-1

Novel potent serine palmitoyl transferase (SPT) inhibitor

1933533-18-6
DCC4865 Sptssb-binder-18

Novel potent and selective binder of small subunit B of the serine palmitoyltransferase complex (SPTSSB)

DCC4866 Spu-106

Novel specific PAK4 inhibitor, effectively inhibiting the invasion of SGC7901 cells without cytotoxicity, regulating the PAK4/LIMK1/cofilin and PAK4/SCG10 signaling pathways

713080-84-3
DCC4867 Sr-01000634273-1

Novel inhibitor of the in vivo aggregation of

882277-05-6
DCC4868 Sr10098

Novel NR4A nuclear receptor modulator

850705-30-5
DCC4869 Sr10658

Novel NR4A nuclear receptor modulator

DCC4870 Sr142948a

Selective neurotensin antagonist

184162-64-9
DCC4871 Sr-17398 Hydrochloride

Novel Unc-51-Like Kinase 1 (ULK1)

1585928-95-5
DCC4872 Sr2067

Novel partial agonist of PPARgamma

DCC4873 Sr24237

Novel NR4A nuclear receptor modulator

1167623-24-6
DCC4874 Sr-3737

Potent inhibitor of both JNK3 and p38

1164153-37-0
DCC4875 Sr-4326

Novel Inhibitor of c-Jun N-terminal Kinase 3 (JNK3)

1164153-25-6
DCC4876 Sr-43845

Novel renin inhibitor

114037-60-4
DCC4877 Sr-58611a

The first selective β3 adrenergic agonist, showing to possess a profile of antidepressant activity in rodents

121524-09-2
DCC4878 Sr8185

Novel Selective TBK1/IKK dual inhibitor with anticancer potency

DCC4879 Srctide

Peptide substrate for many protein kinases, such as Blk, BTK, cKit, EPHA1, EPHB2, EPHB3, ERBB4, FAK, Flt3, IGF-1R, ITK, Lck, MET, MUSK, Ret, Src, TIE2, TrkB, VEGF-R1 (Flt-1) and VEGF-R2 (KDR)

DCC4880 Srebp-in-dhg

Novel inhibitor of sterol regulatory element-binding protein (SREBP), impairing the SREBP activity by inhibiting glucose transporters and thereby activating AMP-activated protein kinase (AMPK)

DCC4881 Sri-22138

Novel mixed μ opioid receptor (MOR) agonist and δ/κ opioid receptor (DOR/KOR) antagonist

DCC4882 Sri-29132

Highly blood-brain barrier permeant, potent, and selective for LRRK2 kinase activity, being effective in attenuating pro-inflammatory responses in macrophages and rescuing neurite retraction phenotypes in neurons.

1482305-44-1
DCC4883 Sri-31040

Potent DAT allosteric modulator, partially inhibiting DAT uptake without altering DAT-mediated reverse transport and with minimal inhibition of DAT binding

1928715-72-3
DCC4884 Sri-35241

Novel inhibitor of thrombospondin 1 activation of TGF-β, blocking TGF-β activation (pIC50 = 8.12 nM) and has a plasma half life of 1.8 h (iv)

2307429-54-3
DCC4885 Sri-36160

Novel potent inhibitor of Wn/ß-catenin signaling in cancer cells

2085682-66-0
DCC4886 Sri-37683

Novel GLUT inhibitor, preferentially inhibiting the growth of GBM cells with minimal toxicity to non-neoplastic astrocytes and neurons, also inhibiting glucose uptake and decrease the glycolytic capacity and glycolytic reserve capacity of GBM patient-deri

DCC4887 Sri-37684

Novel GLUT inhibitor, preferentially inhibiting the growth of GBM cells with minimal toxicity to non-neoplastic astrocytes and neurons, also inhibiting glucose uptake and decrease the glycolytic capacity and glycolytic reserve capacity of GBM patient-deri

DCC4888 Sri-39067

Novel MOR agonist/DOR antagonist that produced systemically active potent antinociceptive activity in tail-flick assay in mice

DCC4889 Srt3025

Novel Sirtuin1 Activator, Down-Regulating Sclerostin and Rescuing Ovariectomy-Induced Bone Loss

1231952-55-8
DCC4890 Srt3025 Hydrochloride

Novel potent SIRT1 activator

2070015-26-6
DCC4891 Srt3190 (2s,3r)

Novel selective CXCR2 antagonist

1204707-73-2
DCC4892 Srta-in-i

Novel potent inhibitor of Staphylococcus aureus sortase A (SrtA)

DCC4893 Ss1020

Novel antiestrogen, lacking estrogenic and genotoxic actions

DCC4894 SS-amyloid-in-7l

Potent ß-amyloid aggregation inhibitor; Antioxidant

DCC4895 SS-carboline-1-carboxylic Acid

Potent competitive inhibitor of indoleamine 2,3-dioxygenase (IDO)

26052-96-0
DCC4896 SS-cit

Non-selective potent dopamine reuptake inhibitor

135416-43-2
DCC4897 SS-cit Tartrate

Non-selective potent dopamine reuptake inhibitor

133647-95-7
DCC4898 SS-elemene

Novel inhibitor of Pak1 activation, anti-cancer ingredient isolated from the Chinese traditional herb Curcuma wenyujin

33880-83-0
DCC4899 SS-hydroxymethyl Chalcone

The first selective inhibitor of Histone Deacetylase 2 (HDAC2)

1613310-15-8
DCC4900 Ssj-183

Novel antimalarial agent

1187533-34-1
DCC4901 SS-lysine

Elongation factor P (EF-P) fuction modifier

4299-56-3
DCC4902 Ssm3 Tfa Salt

Potent furin inhibitor, blocking furin-dependent cell surface processing of anthrax protective antigen-83 in vitro.

922732-52-3
DCC4903 SS-nf-atra

Novel chimeric degrader against cellular retinoic acid binding proteins (CRABPs), inducing the AhR-dependent degradation of CRABP-1 and CRABP-2 via the ubiquitin-proteasome pathway

DCC4904 SS-nf-jq1

Novel chimeric degrader against bromodomain-containing (BRD) proteins, inducing the interaction of AhR and BRD proteins and displaying effective anticancer activity that correlated with protein knockdown activity

DCC4905 SS-nicotinamide Adenine Dinucleotide, Reduced Disodium

Cofactor for mitochondrial deacetylase sirtuin-3 enzyme, regulating energy metabolism and immunity and modulating inflammasome assembly

606-68-8
DCC4906 Ssr126768a

Novel Selective and Orally Active Oxytocin Receptor Antagonist for the Prevention of Preterm Labor

785048-28-4
DCC4907 Ssr180575 Featured

SSR-180,575 is a drug which acts as a selective agonist at the peripheral benzodiazepine receptor, also known as the mitochondrial 18 kDa translocator protein or TSPO. It has been shown to have neuroprotective and cardioprotective effects and to stimulate steroidogenesis of pregnenolone in the brain, which may be linked to its neuroprotective action.

220448-02-2
DCC4908 SS-thujaplicinol

Inhibitor of the replication of herpes simplex viruses 1 and 2 (HSV-1 and HSV-2)

4356-35-8
DCC4909 Sstr3-agonist-5c

Novel non-peptidic highly potent somatostatin receptor 3 (SSTR3) agonist

DCC4910 Sstr3-antagonist-3a

Novel potent sstr3 antagonist, showing to reduce glucose excursion in a mouse oGTT assay

DCC4911 Sstr5a

Novel somatostatin receptor subtype 5 antagonist, stimulating glucoseinduced GLP-1 secretion, reducing blood glucose in a gut- and GLP-1R-dependent manner

DCC4912 St026567

Novel potent mast cell (MC) activator, promoting de novo synthesis of cytokines and inducing the release of eicosanoids from human and mouse MCs

5067-25-4
DCC4913 St029248

Novel potent mast cell (MC) activator, promoting de novo synthesis of cytokines and inducing the release of eicosanoids from human and mouse MCs

96-69-5
DCC4914 St056083

Novel inhibitor of the c-di-AMP synthetase DNA integrity scanning protein (DisA) in vitro

299419-24-2
DCC4915 St101036

Novel potent mast cell (MC) activator, promoting de novo synthesis of cytokines and inducing the release of eicosanoids from human and mouse MCs

1018143-39-9
DCC4916 st-1032

Novel histamine H3 receptor ligand

DCC4917 St1237

Potent, direct, non-cytotoxic Arachidonate_5-lipoxygenase>5-lipoxygenase (5-LO) inhibitor

1380593-17-8
DCC4918 St-161

Antiviral agent against LASV and a number of other viruses in the Arenaviridae family

DCC4919 St-1703

Novel histamine H3 receptor ligand

DCC4920 St-1892

Novel highly potent and soluble partial FXR agonist

1409411-32-0
DCC4921 St-198

Seletive dopamine D3 receptors

854924-64-4
DCC4922 St-1992

Novel potent A 1 R/A 2A R/H 3 R multitargeting ligand (MTL)

DCC4923 St-2001

Novel potent A 1 R/A 2A R/H 3 R multitargeting ligand (MTL)

DCC4924 St-2262

Novel selective NaV1.7 inhibitor, blocking the extracellular vestibule of the channel with an IC50 of 72 nM and greater than 200-fold selectivity over off-target sodium channel isoforms, NaV1.1-1.6 and NaV1.8

DCC4925 St4070

Highly selective FAAH>fatty acid amide hydrolase (FAAH) inhibitor

1186236-75-8
DCC4926 St7710aa1

Novel PARP-1 inhibitor, showing significant in vitro target inhibition and capability to substantially bypass the multidrug resistance mediated by Pgp

1542067-20-8
DCC4927 Sta-9584

Novel tubulin-binding vascular disrupting agent (VDA)

906481-23-0
DCC4928 Stad-2

Cell permeable AKAP disruptor, selectively binding to PKA-RII and blocking the interaction of PKA-RI with AKAP

1542100-77-5
DCC4929 Stalobacin I

Novel Lipopeptide Antibiotic with Potent Antibacterial Activity against Multidrug-Resistant Bacteria

DCC4930 Stanozolol [10418-03-8]

Anabolic-androgenic steroid (AAS), acting as an agonist of the androgen receptor (AR)

10418-03-8
DCC4931 Stat3 -in-11

Novel STAT3 inhibitor, selectively inhibiting STAT3 phosphorylation and exhibiting potent antitumor activity

DCC4932 stat3 Inhibitor 6

Novel inhibitor of STAT3 signaling pathway

665014-97-1
DCC4933 Stat3-in-13r

Novel inhibitor of STAT3, targeting SH2 domain

DCC4934 Stat3-in-3

Novel potent and selective inhibitor of STAT3

2361304-26-7
DCC4935 Stat3-in-a69

Novel inhibitor targeting the DNA-binding domain of STAT3, suppressing tumor growth, metastasis and STAT3 target gene expression in vivo

1164546-70-6
DCC4936 Stat3-in-b9

Novel inhibitor of signal transducer and activator of transcription 3 (STAT3), inhibiting the proliferation of tumor cells harboring abnormal activation of STAT3, such as, MDA-MB-468, MDA-MB-231 and DU145

825611-06-1
DCC4937 Stat5a-in-27

Novel cell-permeable selective STAT5a inhibitor prodrug, inhibiting tyrosine phosphorylation of STAT5a with selectivity over STAT5b in cultured human leukemia cells, and representing a valuable tool to define the non-redundant molecular functions of the t

DCC4938 Stat5b-in-6a

Highly Potent and Selective Inhibitor of the Transcription Factor STAT5b

DCC4939 Stemazole

Novel human stem/progenitor cells proliferation activator, promoting survival and preserving stemness in human embryonic stem cells

317337-07-8
DCC4940 Sterigmatocystin

Natural inducer of G1 arrest in primary human esophageal epithelial cells but G2 arrest in immortalized cells

10048-13-2
DCC4941 Stf-038533

Novel inhibitor of expression from canonical CREB response element-containing promoters

423744-59-6
DCC4942 Stg -001

Novel RBP4 antagonist for treatment of Stargardt disease

DCC4943 Stictic Acid

Natural anti-feline infectious peritonitis virus (FIPV) agent, specifically targeting the 3CLpro of FIPV and inhibiting its replication

549-06-4
DCC4944 Sting Agonist 11

Novel non-nucleotide STING agonist, demonstrating antitumor activity when dosed intratumorally in a syngeneic mouse model

DCC4945 Sting Inhibitor C-171

Novel covalent antagonist of hsSTING

DCC4946 Stk-15

Novel Fatty Acid Binding Protein 5 (FABP5) Inhibitor

844651-66-7
DCC4947 Stk-22

Novel Fatty Acid Binding Protein 5 (FABP5) Inhibitor

843629-43-6
DCC4948 Stk295900

Dual inhibitor of topoisomerase 1 and 2, inducing G(2) arrest in the absence of DNA damage. Inhibitor of Plasmodium falciparum W2 (drug-resistant) proliferation in erythrocyte-based infection assay

4402-17-9
DCC4949 Stk508411

Novel inhibitor of the heterogeneous ribonuclear protein A18 (hnRNP A18)

664968-32-5
DCC4950 Stk630921

Novel blocker of IL-17A binding to the IL-17A receptor (IL-17RA)

1033850-63-3
DCC4951 Stk683963

Novel activator of cellular ATG4B activity

370073-65-7
DCC4952 Stock1n-65837

Potent natural modulator of human Toll-like receptor 7 (TLR7)

DCC4953 Streptolidine

Metablite of the Streptomyces antibiotics streptothricin and streptolin

29307-61-7
DCC4954 Streptozocin

Antibiotic, being used as an antineoplastic agent and to induce diabetes in experimental animals

18883-66-4
DCC4955 Sts-e412

The first nonpeptidyl, selective activator of the tissue-protective EPOR/CD131 receptor

1609980-39-3
DCC4956 Sts-e424

Novel agonist of the tissue-protective erythropoietin (EPO) receptor, increasing FXN expression and EPOR phosphorylation

DCC4957 Stx-2622

Inhibitor of 17β-hydroxysteroid dehydrogenases (17β-HSDs)

37075-05-1
DCC4958 Stx2845

Novel Nonsteroidal Inhibitor of Carbonic Anhydrase IX

1623785-66-9
DCC4959 Su0383

Novel dual Inhibitor of repair enzymes 8-oxoguanine DNA glycosylase (OGG1) and human MutT Homolog 1 (NUDT1 or MTH1), increasing sensitivity of tumor cells to oxidative stress

DCC4960 Su11272

Novel potent c-MET inhibitor

669764-16-3
DCC4961 Su11606

Potent c-MET inhibitor

669764-17-4
DCC4962 Su11652

Sunitinib analog, acting as a potential inhibitor for nucleoside diphosphate kinase (NDK) from Leishmania major (LmNDK)

326914-10-7
DCC4963 Su-200

Agonist of TRPV1

184003-14-3
DCC4964 Su9518

Novel potent and selective inhibitor of the cellular PDGF receptor kinase and PDGF receptor-induced cell proliferation

251356-32-8
DCC4965 Subglutinol A

Natural immunosuppressive agent, effectively blocking T cell proliferation and survival while profoundly inhibiting pro-inflammatory IFNγ and IL-17 production by fully differentiated effector Th1 and Th17 cells, also acting as an estrogen receptor antagon

DCC4966 Suc-leu-leu-val-tyr-amc

Fluorescent substrate which can be hydrolyzed by the proteasome to release free AMC and the fluorescence of which is proportional to the proteasome activity

94367-21-2
DCC4967 Sucnr1-in-20

Novel antagonist of G-protein-coupled receptor SUCNR1 (succinate receptor 1 or GPR91)

DCC4968 Suku-33

Novel potent inhibitor of osteoclastogenesis, suppressing both equilibrative nucleoside transporters and concentrative nucleoside transporters

DCC4969 Sul-121 Hydrochloride

Novel inhibitor of airway inflammation and hyperresponsiveness in experimental models of chronic obstructive pulmonary disease (COPD)

1541170-25-5
DCC4970 Sulfacetamide

Antibacterial, inhibiting bacterial folic acid synthesis by competing with para amino benzoic acid

114-80-9
DCC4971 Sulfazecin

β-Lactam antibiotic against multi-drug resistant pathogens

77912-79-9
DCC4972 Sulfonyl Quinoxaline 1

Novel inhibitor of RhoG-hepcidin uptake

338394-53-9
DCC4973 Sulfosuccinimidyl Oleate Sodium

Neuroprotective agent, alleviating stroke-induced neuroinflammation

135661-44-8
DCC4974 Suloctidil Hydrochloride

Peripheral vasodilator

54767-71-4
DCC4975 Sulukast

Novel, potent, selective, and competitive antagonist of LTD4 and LTE4

98116-53-1
DCC4976 Sumanirole

D2 selective dopamine agonist, showing anxiolytic and anti-parkinsonian activities

179386-43-7
DCC4977 Sun13837

Novel fibroblast growth factor receptor modulator for treating neurodegenerative diseases

DCC4978 Sun-c5174

5-HT2 antagonist

191592-36-6
DCC4979 Supradamal

Potent Inhibitor of Plasmodium FK506 Binding Protein 35 (FKBD35), also act as a HIV inhibitor

71458-51-0
DCC4980 suvanine

Antagonist of the mammalian bile acid sensor farnesoid-X-receptor (FXR)

94203-53-9
DCC4981 Sv-293

Selective D2 dopamine receptor antagonist

873445-73-9
DCC4982 Sv-iii-130s

D2 dopamine receptor partial agonist in adenylyl cyclase inhibition assay and antagonist in the GIRK and phospho ERK1/2 assays

129722-23-2
DCC4983 Sw208108

Novel clickable tumor-specific irreversible inhibitor of stearoyl CoA desaturase (SCD)

1673557-43-1
DCC4984 Swainsonine

Natural potent alpha-mannosidase inhibitor, exhibiting antimetastatic, antiproliferative, and immunomodulatory activities

72741-87-8
DCC4985 swertisin

Potent differentiating agent

6991-10-2
DCC4986 S-y048

Novel selective OXE receptor antagonist

DCC4987 Sy-5609

Novel highly potent and selective CDK7 inhibitor, demonstrating broad anti-tumor activity in vivo

DCC4988 Syk-524

Novel universal opioid receptor agonist

DCC4989 Syk-in-ii

Novel inhibitor of the Syk kinase (spleen tyrosine kinase)

1345458-66-3
DCC4990 Syn-1 Peptide

Novel potent and specific inhibitor of syncytin-mediated cell fusion, completely blocking cell fusion at 1.6 μg/ml

DCC4991 Syn-1 Scr Peptide

Negative control of Syn-1 peptide, having the same amino acid composition as Syn-1 peptide, but a scrambled sequence

DCC4992 syn22269076

Novel Mycobacterium tuberculosis growth inhibitor

1214506-05-4
DCC4993 Synstab A

Novel microtubule-stablizer

257612-36-5
DCC4994 Synthalin Dihydrochloride

K+ channel blocker

301-15-5
DCC4995 Szu101

Novel TLR7 agonist via immune response induction and tumor microenvironment modulation

<Prev1...176177178179180...191Next>