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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
20661HFY-4A2094810-82-798% Min.
HFY-4A is a HDAC inhibitor. HFY-4A inhibits breast cancer cell proliferation, migrati
20658Hynic-TOC257943-19-498% Min.
Hynic-TOC is a ligand for making 99mTc-Hynic-TOC as an imaging agent in the diagnosti
20568HDAC-IN-582071224-39-898% Min.
HDAC-IN-58 is a HDAC inhibitor.
205211H-1,2,3-triazole, 4,5-diiodo-28194-09-498% Min.
20517HM432392569527-64-498% Min.
HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibit
204824(3H)-Pyrimidinone, 5-bromo-6-cyclopropyl-27192-20-798% Min.
204302(1H)-Pyridinone, 5,6-dihydro-4-(4-methylphenyl)-3-(2H-tetrazol-5-yl)-6-[4-(4,4,4-trifluorobutoxy)phenyl]-6-(trifluoromethyl)-, (6S)-1441057-15-398% Min.
204221H-Indazole-1-acetic acid, 3-acetyl-5-bromo-, 1,1-dimethylethyl ester2086183-72-298% Min.
204101H-Pyrrolo[2,3-b]pyridine, 4-chloro-1-[tris(1-methylethyl)silyl]-651744-48-898% Min.
204044-hydroxybiphenyl-4-carboxamide182318-78-198% Min.
203881H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, ethyl ester221675-35-098% Min.
203716-Hydroxyl-2-tetralone52727-28-398% Min.
210201HISPOLON(P)173933-40-998% Min.
20123101HMPL-5231415792-84-5≧98.0%
HMPL-523 is a novel, highly selective and potent small molecule oral inhibitor target
20919105-Hydroxymethyldeoxyuridine5116-24-598% Min.
5-Hydroxymethyldeoxyuridine is a nucleoside analog with anticancer and antiviral acti
20912045-hydroxy-2,4-dimethylpyrimidine412003-95-3≧96.0%
2,4-dimethylpyrimidin-5-ol is a key intermidiate ofLemborexant. Kg scale may be provi
2071633H-BETA-ALA-AMC TFA201847-54-398% Min.
20620062'-HYDROXY-6'-METHOXYACETOPHENONE703-23-196% Min.
206104HC-0701628291-95-198% Min.
HC-070 is a potent inhibitor of TRPC4 and TRPC5, leading to anxiolytic and antidepres
204610Hydroxyfasudil HCl155558-32-0 (HCl)98% Min.
Hydroxyfasudil, aslo known as HA1100, is a cell-permeable hydroxylated metabolite of
19317HBX-41108 924296-39-9>98%
HBX 41108 is an inhibitor of ubiquitin-specific protease (USP) 7. HBX 41108 inhibits
192223HS-13712158197-70-5>98%
HS-1371 is a novel kinase inhibitor of RIP3-mediated necroptosis. HS-1371 directly bi
19182HZ-11571009734-33-1>98%
HZ-1157 is a hepatitis C virus (HCV) inhibitor with inhibitory activities toward HCV
1811022H 151941987-60-6>98%
H 151 is a STING antagonist that covalently binds STING at Cys91, blocking palmitoyla
1810171HC-0564567733-96-2>98%
HC-056456 is a CatSper channel modulator.
18528320-HETE79551-86-3>98%
20-HETE is a cytochrome P450 (CYP450) metabolite postulated to play an autacoid role
184122HMN-154173528-92-2>98%
HMN-154 is a benzenesulfonamide anticancer agent. HMN-154 inhibits DNA binding of NF-
1710133HJC01521420290-99-8>98%
HJC0152 is a signal transducer and activator of transcription 3 (STAT3) inhibitor aga
17913139-Hydroxyellipticin(free base)51131-85-298.0%
9-hydroxyellipticine, also known as IGIG 929 and LS133324, is a potent cytotoxic and
179822H3B-65271702259-66-298.0%
H3B-6527 is a potent and orally active FGFR4 inhibitor with potential antineoplastic