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Cat. No. Product name CAS No.
DC8419 SB-334867 Featured

SB-334867 is a selective orexin-1 (OX1) receptor antagonist.

792173-99-0
DC9735 SB-366791 Featured

SB-366791 is a selective and competitive VR1 (TRPV1) antagonist that is commonly used in pain research.

472981-92-3
DC8483 SB-399885 HCl Featured

Potent, brain penetrant, orally active 5-HT6 antagonist. Displays > 200-fold selectivity for 5-HT6 over other 5-HT receptors (pKi values are 9.11, 8.81 and 9.02 for human recombinant, native rat and native human 5-HT6 receptors respectively).

402713-80-8
DC7670 SB-3CT Featured

SB-3CT is an effective and selective gelatinase inhibitor with Ki of 13.9 nM and 600 nM for MMP-2 and MMP-9, respectively.

292605-14-2
DC7277 SB-408124 Featured

SB408124 is a non-peptide antagonist for OX1 receptor with Ki of 57 nM and 27 nM in both whole cell and membrane, respectively; exhibits 50-fold selectivity over OX2 receptor.

288150-92-5
DC5189 SB-431542 Featured

SB431542 is a potent and selective inhibitor of ALK5 with IC50 of 94 nM, 100-fold more selective for ALK5 than p38 MAPK and other kinases.

301836-41-9
DC7278 SB-505124 Featured

SB505124 is a selective inhibitor of TGFβR for ALK4, ALK5 with IC50 of 129 nM and 47 nM, respectively, also inhibits ALK7, but does not inhibit ALK1, 2, 3, or 6.

694433-59-5
DC6312 SB525334 Featured

SB525334 is a potent and selective inhibitor of TGFβ receptor I (ALK5) with IC50 of 14.3 nM, is 4-fold less potent to ALK4 than ALK5 and inactive to ALK2, 3, and 6.

356559-20-1
DC7279 SB-590885 Featured

SB590885 is a potent B-Raf inhibitor with Ki of 0.16 nM, 11-fold greater selectivity for B-Raf over c-Raf, no inhibition to other human kinases.

405554-55-4
DC22415 SB-612111 Featured

SB-612111 is a potent, selective nociceptin/orphanin FQ receptor (NOP receptor) antagonist with Ki of 0.33 nM.

371980-98-2
DC9573 SB-674042 Featured

SB-674042 is a potent and selective non-peptide orexin OX1 receptor antagonist (Kd = 3.76 nM); exhibits 100-fold selectivity for OX1 over OX2 receptors.

483313-22-0
DC9635 SB-705498 Featured

SB-705498 is a potent, selective and orally bioavailable transient receptor potential vanilloid 1 (TRPV1) receptor antagonist with a pIC50 of 7.1.

501951-42-4
DC8354 Intepirdine (SB-742457, RVT-101) Featured

SB-742457(RVT-101) is a selective 5-HT6 receptor antagonist with potential cognition, memory, and learning-enhancing effects.

607742-69-8
DC5137 SB 743921 Featured

SB743921 is a kinesin spindle protein (KSP) inhibitor with Ki of 0.1 nM, almost no affinity to MKLP1, Kin2, Kif1A, Kif15, KHC, Kif4 and CENP-E.

940929-33-9
DC10470 SB756050 Featured

SB-756050 is a Farnesoid X receptor (FXR) (NR1H4) agonist.

447410-57-3
DC10729 SB9200(Inarigivir soproxil) Featured

SB9200(Inarigivir soproxil) is a novel agonist of innate immunity, shows potent antiviral activity against resistant HCV variants.

942123-43-5
DC10148 SBC-110736 Featured

SBC-110736 is a novel inhibitor of proprotein convertase subtilisin kexin type 9 (PCSK9), lowering cholesterol levels in mice.

1629166-02-4
DC8349 SBC-115076 Featured

SBC-115076 is an anti-proprotein convertase subtilisin kexin type 9 (anti-PCSK9) compounds, for the treatment and/or prevention of cardiovascular diseases.

489415-96-5
DC7965 SBE 13 hydrochloride Featured

SBE13 Hcl is a potent and selective PLK1 with IC50 of 0.2 nM; no inhibition om Aurora A kinase, Plk2 and Plk3.

1052532-15-6
DC8316 SBI-0206965 Featured

SBI-0206965 is a potent, selective and cell permeable autophagy kinase ULK1 inhibitor.

1884220-36-3
DC10511 SBI-0640756 Featured

SBI-0640756(SBI-756) is a first-in-class inhibitor that targets eIF4G1 and disrupts the eIF4F complex.

1821280-29-8
DC24210 SBI-115 Featured

SBI-115 is a TGR5 (GPCR19) antagonist. SBI-115 decreases hepatic cystogenesis with polycystic liver diseases via inhibiting TGR5.

882366-16-7
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