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 |