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Home > Products
| Cat.No. | Product name | Product Description |
| R10162 | Apremilast; CC10004 | Apremilast (CC-10004) is a potent and orally active PDE4 and TNF-α inhibitor wit |
| R10164 | Avibactam sodium; NXL-104 | Avibactam sodium(NXL-104) is a non-β-lactam β-lactamase inhibitor antibiotic. |
| R10167 | PI103 Free base | PI-103 is a multi-targeted PI3K inhibitor for p110α/β/δ/γ with IC50 of 2 nM/3 nM |
| R10168 | YM201636 | YM201636 is a selective PIKfyve inhibitor with IC50 of 33 nM, less potent to p11 |
| R10174 | PF429242 | PF 429242 is a reversible, competitive inhibitor of sterol regulatory element-bi |
| R10177 | GSK364735 | |
| R10179 | 4SC201 | Resminostat dose-dependently and selectively inhibits HDAC1/3/6 with IC50 of 42. |
| R10180 | Torin2 | Torin 2 is a potent and selective mTOR inhibitor with IC50 of 0.25 nM in p53−/− |
| R10181 | AP24534; Ponatinib | Ponatinib (AP24534) is a novel, potent multi-target inhibitor of Abl, PDGFRα, VE |
| R10184 | GW9508 | GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 10 |
| R10185 | Otenabant Hydrochloride (CP 945598 Hydrochloride) | Otenabant (CP-945598) HCl is a potent and selective cannabinoid receptor CB1 ant |
| R10186 | CP945598 free base | Otenabant (CP945598) is a recently discovered selective, high affinity, competit |
| R10188 | ciproxifan; FUB359 | Ciproxifan is a highly potent and selective histamin H3-receptor antagonist with |
| R10189 | AT7519 HCl | AT7519 HCl is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10-210 |
| R10190 | BIX02188 | BIX02188 is a selective inhibitor of MEK5 with IC50 of 4.3 nM, also inhibits ERK |
| R10191 | Tacedinaline (N-acetyldinaline; CI-994; Goe-5549) | CI994 (Tacedinaline) is an anti-cancer drug which inhibits HDAC1 with IC50 of 0. |
| R10192 | ZM323881HCl | ZM 323881 is a potent and selective VEGFR2 inhibitor with IC50 of <2 nM, almo |
| R10193 | ZM 306416 (Synonyms: CB 676475) | ZM 306416 is a VEGFR (Flt and KDR) inhibitor for VEGFR1 with IC50 of 0.33 μM, bu |
| R10194 | OC000459 | OC000459 is a potent and selective D prostanoid receptor 2 (DP2) antagonist with |
| R10195 | Enasidenib; AG221 | Enasidenib is a oral potent, selective, reversible inhibitor of mutant IDH2. |
| R10197 | AZ-33 | AZ-33： 2-(4-(4-(3-(2-methylbenzo[d]thiazol-6-ylamino)-3-oxopropylamino)-4-oxobut |
| R10201 | IP145; Duvelisib; Impurity comparison | |
| R10202 | AZD4547 | AZD4547 is a novel selective FGFR inhibitor targeting FGFR1/2/3 with IC50 of 0.2 |
| R10204 | PF562271 | PF-562271 is a potent, ATP-competitive, reversible inhibitor of FAK wi |
| R10209 | indisulam; E7070 | Indisulam (E7070) is a carbonic anhydrase inhbitor, is also a novel synthetic su |
