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Cat. No. Product name CAS No.
DC9841 Fostamatinib(R788) Featured

R788 (Fostamatinib), a prodrug of the active metabolite R406, is a potent Syk inhibitor with IC50 of 41 nM.

901119-35-5
DC1013 R788 disodium (Fostamatinib) Featured

R935788 (Fostamatinib disodium, R788) is a Syk inhibitor with IC50 of 41 nM.

1025687-58-4
DC9513 Radafaxine (hydrochloride) Featured

Radafaxine Hcl(BW-306U; GW-353162A) is a potent metabolite of bupropion; selective for inhibiting the reuptake of norepinephrine over dopamine; DAT (dopamine transporter) and NET(norepinephrine transporter) transporters inhibitor, and nAChR family modulat

106083-71-0
DC5049 RAF265 (CHIR-265) Featured

RAF265 (CHIR-265) is a highly selective B-Raf and VEGFR2 inhibitor with IC50 of 3-60 nM and EC50 of 30 nM, including B-Raf, C-Raf and mutant B-Raf.

927880-90-8
DC8930 Rafoxanide

Rafoxanide is a salicylanilide used as an antiparasitic agent.

22662-39-1
DC9479 Raltegravir (potassium salt)

Raltegravir potassium salt(MK0518 potassium salt) is a potent integrase (IN) inhibitor, used to treat HIV infection.

871038-72-1
DCAPI1581 Raltegravir Featured

Raltegravir Salt is a potent human immunodeficiency virus (HIV) integrase inhibitor and a novel anti-AIDS drug.

518048-05-0
DC8940 Raltitrexed Featured

Raltitrexed(ZD1694), an inhibitor of thymidylate synthase, is an antimetabolite drug used in cancer chemotherapy.

112887-68-0
DC9162 Ranolazine HCl Featured

Ranolazine(RS-43285) is an antianginal agent with antiarrhythmic properties that achieves its effects via a novel mechanism of action (inhibition of the late phase of the inward sodium current), without affecting heart rate or blood pressure (BP).

95635-56-6
DC1048 Rapamycin (Sirolimus) Featured

Rapamycin (Sirolimus, AY-22989, WY-090217) is a specific mTOR inhibitor with IC50 of ~0.1 nM. -

53123-88-9
DC8175 Rapastinel(GLYX-13) Featured

Rapastinel(GLYX-13) is a NMDA receptor partial agonist that acts at the glycine site.

117928-94-6
DC8190 Ravidasvir hydrochloride (PPI-668) Featured

Ravidasvir(PPI-668) is a NS5A Inhibitor.

1303533-81-4
DC7808 Refametinib (BAY86-9766) Featured

Refametinib (RDEA119, Bay 86-9766) is a potent, ATP non-competitive and highly selective inhibitor of MEK1 and MEK2 with IC50 of 19 nM and 47 nM, respectively.

923032-37-5
DC9777 Regorafenib monohydrate(BAY 73-4506) Featured

Regorafenib (BAY 73-4506) is a multi-target inhibitor for VEGFR1, VEGFR2, VEGFR3, PDGFRβ, Kit, RET and Raf-1 with IC50 of 13 nM/4.2 nM/46 nM, 22 nM, 7 nM, 1.5 nM and 2.5 nM, respectively.

1019206-88-2
DC1030 Regorafenib (BAY73-4506,Fluoro-Sorafenib) Featured

Regorafenib (BAY 73-4506, Fluoro-Sorafenib) is a multi-target inhibitor for VEGFR1, VEGFR2, VEGFR3, PDGFRβ, Kit, RET and Raf-1 with IC50 of 13 nM/4.2 nM/46 nM, 22 nM, 7 nM, 1.5 nM and 2.5 nM, respectively.

755037-03-7
DC10441 Relebactam Featured

Relebactam is a diazabicyclooctane inhibitor with activity against a wide spectrum of β-lactamases, including class A (extended-spectrum β-lactamases [ESBLs] and KPC) and class C (AmpC) enzymes.

1174018-99-5
DC10463 Repotrectinib(TPX-005) Featured

Repotrectinib(TPX-005) is a multi-target macrocycle inhibitor of anaplastic lymphoma kinase (ALK), c-ros proto-oncogene 1 receptor tyrosine kinase (ROS1), and neurotrophic tyrosine kinase receptor (TRK)

1802220-02-5
DC7261 Resminostat hydrochloride (4SC-201)

Resminostat(RAS2410; 4SC-201) is a potent inhibitor of HDAC1/3/6(IC50=43-72 nM); less potent to HDAC8 with IC50 of 877 nM.

1187075-34-8
DC4148 Retapamulin

Retapamulin is a topical antibiotic, which binds to both E. coli and S. aureus ribosomes with similar potencies with Kd of 3 nM.

224452-66-8
DC10191 RG7800

RG7800 a small molecule SMN2 splicing modifier to enter human clinical trials to treat spinal muscular atrophy.

1449598-06-4
DC8185 Verosudil(AR-12286)

Rho-kinase (ROCK) inhibitor

1414854-42-4
DCAPI1165 Ribavirin (Copegus) Featured

Ribavirin is a guanosine analog with antiviral properties against DNA and RNA viruses, including respiratory syncytial virus, hepatitis C, and influenza.

36791-04-5
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