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Home > Products
| Cat.No. | Product name | Product Description |
| R11965 | IOX4 | IOX4 is a selective HIF prolyl-hydroxylase 2 (PHD2) inhibitor with an IC50& |
| R11966 | ARN-3236 | ARN-3236 is an oral active and selective inhibitor of salt-inducible kinase |
| R11967 | GDC-0575 (ARRY-575, RG7741) | GDC-0575 (ARRY-575, RG7741) is a highly-selective oral small-molecule Chk1& |
| R11949 | FGH-10019 | FGH10019 is a novel sterol regulatory element-binding protein (SREBP) inhibitor |
| R11969 | SB 203580 hydrochloride (RWJ 64809 hydrochloride) | SB 203580 hydrochloride (RWJ 64809 hydrochloride) is a widely used p38 MAPK |
| R11968 | AT9283 | AT9283 is a potent JAK2/3 inhibitor with IC50&nb |
| R11970 | Fasudil (Synonyms: HA-1077; AT877) | Fasudil (HA-1077; AT877), is a nonspecific ROCK inhibitor and also has inhibitor |
| R11971 | Domatinostat tosylate (4SC-202) | Domatinostat tosylate (4SC-202) is a selective class I HDAC inhibitor |
| R11973 | PF-4136309 (Synonyms: INCB8761) | PF-4136309 is a potent, selective, and orally bioavailable CCR2 antagonist, with |
| R11972 | DMH1 | DMH-1 is a potent and selective BMP inhibitor with IC50s of 27/10 |
| R11975 | Prexasertib (LY2606368) | Prexasertib (LY2606368) is a potent, selective and ATP-competitive checkpoi |
| R11976 | Prexasertib dihydrochloride (Synonyms: LY2606368 (dihydrochloride)) | Prexasertib dihydrochloride (LY2606368 dihydrochloride) is a potent and selectiv |
| R11978 | AUZ454 (K03861) | AUZ 454 (K03861) is a type II CDK2 inhibitor with Kd of 8.2 |
| R11979 | Compound E;Compound E (secretase inhibitor)；DuPont E) | Compound E is a γ-secretase inhibitor. Compound E bloks β-amyloid(40), |
| R11980 | GSK2982772 | GSK2982772 is a potent, orally active and ATP competitive RIP1 kinase inhibitor |
| R11981 | Cerdulatinib (PRT062070) | Cerdulatinib (PRT062070) is a selective Tyk2 inhibitor with an IC |
| R11982 | Autophinib | Autophinib is a potent, selective autophagy inhibitor with IC50s |
| R11983 | BBT594 | BBT594 is a potent receptor tyrosine kinase RET inhibitor, used for cancer |
| R11984 | AST 487 | AST 487 is a RET kinase inhibitor with IC50 of 880 nM, inhib |
| R11985 | H3B-6527 | H3B-6527 is an orally active, highly selective and covalent FGFR4 inhi |
| R11987 | SAR-20347 | SAR-20347 is an inhibitor of TYK2, JAK1, JAK2 and JAK3& |
| R11988 | ON-123300;ON123300 | ON123300 is a potent inhibitor of CDK4, with an IC50 of 3.8 nM, with little inhi |
| R11989 | PD-166285 dihydrochloride;PD-166285 2HCl;PD166285 dihydrochloride | PD 166285, a novel protein tyrosine kinase inhibitor of a new structural class, |
| R11990 | PD-161570;PD161570 | N/A |
| R11991 | PRN1371 | PRN1371 is a highly selective and potent FGFR1-4 and CSF1R i |
