Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
20661 | HFY-4A | 2094810-82-7 | 98% Min. | |
HFY-4A is a HDAC inhibitor. HFY-4A inhibits breast cancer cell proliferation, migrati | ||||
20658 | Hynic-TOC | 257943-19-4 | 98% Min. | |
Hynic-TOC is a ligand for making 99mTc-Hynic-TOC as an imaging agent in the diagnosti | ||||
20568 | HDAC-IN-58 | 2071224-39-8 | 98% Min. | |
HDAC-IN-58 is a HDAC inhibitor. | ||||
20521 | 1H-1,2,3-triazole, 4,5-diiodo- | 28194-09-4 | 98% Min. | |
20517 | HM43239 | 2569527-64-4 | 98% Min. | |
HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibit | ||||
20482 | 4(3H)-Pyrimidinone, 5-bromo-6-cyclopropyl- | 27192-20-7 | 98% Min. | |
20430 | 2(1H)-Pyridinone, 5,6-dihydro-4-(4-methylphenyl)-3-(2H-tetrazol-5-yl)-6-[4-(4,4,4-trifluorobutoxy)phenyl]-6-(trifluoromethyl)-, (6S)- | 1441057-15-3 | 98% Min. | |
20422 | 1H-Indazole-1-acetic acid, 3-acetyl-5-bromo-, 1,1-dimethylethyl ester | 2086183-72-2 | 98% Min. | |
20410 | 1H-Pyrrolo[2,3-b]pyridine, 4-chloro-1-[tris(1-methylethyl)silyl]- | 651744-48-8 | 98% Min. | |
20404 | 4-hydroxybiphenyl-4-carboxamide | 182318-78-1 | 98% Min. | |
20388 | 1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, ethyl ester | 221675-35-0 | 98% Min. | |
20371 | 6-Hydroxyl-2-tetralone | 52727-28-3 | 98% Min. | |
210201 | HISPOLON(P) | 173933-40-9 | 98% Min. | |
20123101 | HMPL-523 | 1415792-84-5 | ≧98.0% | |
HMPL-523 is a novel, highly selective and potent small molecule oral inhibitor target | ||||
2091910 | 5-Hydroxymethyldeoxyuridine | 5116-24-5 | 98% Min. | |
5-Hydroxymethyldeoxyuridine is a nucleoside analog with anticancer and antiviral acti | ||||
2091204 | 5-hydroxy-2,4-dimethylpyrimidine | 412003-95-3 | ≧96.0% | |
2,4-dimethylpyrimidin-5-ol is a key intermidiate ofLemborexant. Kg scale may be provi | ||||
2071633 | H-BETA-ALA-AMC TFA | 201847-54-3 | 98% Min. | |
2062006 | 2'-HYDROXY-6'-METHOXYACETOPHENONE | 703-23-1 | 96% Min. | |
206104 | HC-070 | 1628291-95-1 | 98% Min. | |
HC-070 is a potent inhibitor of TRPC4 and TRPC5, leading to anxiolytic and antidepres | ||||
204610 | Hydroxyfasudil HCl | 155558-32-0 (HCl) | 98% Min. | |
Hydroxyfasudil, aslo known as HA1100, is a cell-permeable hydroxylated metabolite of | ||||
19317 | HBX-41108 | 924296-39-9 | >98% | |
HBX 41108 is an inhibitor of ubiquitin-specific protease (USP) 7. HBX 41108 inhibits | ||||
192223 | HS-1371 | 2158197-70-5 | >98% | |
HS-1371 is a novel kinase inhibitor of RIP3-mediated necroptosis. HS-1371 directly bi | ||||
19182 | HZ-1157 | 1009734-33-1 | >98% | |
HZ-1157 is a hepatitis C virus (HCV) inhibitor with inhibitory activities toward HCV | ||||
1811022 | H 151 | 941987-60-6 | >98% | |
H 151 is a STING antagonist that covalently binds STING at Cys91, blocking palmitoyla | ||||
1810171 | HC-056456 | 7733-96-2 | >98% | |
HC-056456 is a CatSper channel modulator. | ||||
185283 | 20-HETE | 79551-86-3 | >98% | |
20-HETE is a cytochrome P450 (CYP450) metabolite postulated to play an autacoid role | ||||
184122 | HMN-154 | 173528-92-2 | >98% | |
HMN-154 is a benzenesulfonamide anticancer agent. HMN-154 inhibits DNA binding of NF- | ||||
1710133 | HJC0152 | 1420290-99-8 | >98% | |
HJC0152 is a signal transducer and activator of transcription 3 (STAT3) inhibitor aga | ||||
1791313 | 9-Hydroxyellipticin(free base) | 51131-85-2 | 98.0% | |
9-hydroxyellipticine, also known as IGIG 929 and LS133324, is a potent cytotoxic and | ||||
179822 | H3B-6527 | 1702259-66-2 | 98.0% | |
H3B-6527 is a potent and orally active FGFR4 inhibitor with potential antineoplastic |
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