| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 51803 | Semaxanib (SU5416) | 204005-46-9 | 98% | ![]() |
| Semaxanib (SU5416) is a potent and selectiveVEGFR(Flk-1/KDR) inhibitor withIC50of 1.2 | ||||
| 102703 | AZD-8835 | 1620576-64-8 | ≧98.0% | ![]() |
| AZD8835 is a potent and selective inhibitor of PI3Kalpha and PI3Kdelata with excellen | ||||
| 184321 | Ensartinib ( X396 ) | 1370651-20-9 | >98% | ![]() |
| Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k | ||||
| 26A016 | iMQT_020 | 2463893-46-9 | ≧98.0% | ![]() |
| iMQT_020 is a specific small molecule inhibitor targeting mitochondrial SLC1A5_var (a | ||||
| 26A009 | Velzatinib (IDRX-42, M-4205) | 2590556-80-0 | ≧98.0% | ![]() |
| Velzatinib is an orally bioavailable small molecule inhibitor of multiple mutated for | ||||
| 26A010 | DPTX-3186 | ≧98.0% | ![]() | |
| DPTX3186, an orally administered small molecule condensate modulator (c-mod) inhibiti | ||||
| 26A011 | Iadademstat ( ORY-1001 ) hydrochloride | 1431303-72-8 | ≧98.0% | ![]() |
| Iadademstat (ORY-1001) is an orally active, highly potent and selective inhibitor of | ||||
| 26A018 | AD-8007 | 1497439-74-3 | ≧98.0% | ![]() |
| AD-8007 is a selective and brain-penetrant inhibitor of acetyl CoA synthase 2 (ACSS2). | ||||
| 26A021 | MAT2A-IN-22 | 2925330-18-1 | ≧98.0% | ![]() |
| MAT2A-IN-22 (Compound 29-1) is a blood-brain barrier-penetrant and orally active MAT2 | ||||
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