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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
179117AMG-9810545395-94-698.0%
AMG 9810 is a competitive antagonist of capsaicin activation of the vanilloid recepto
179832AS-2444697 HCl1287665-60-498.0%
AS-2444697 is a RAK-4 inhibitor. Six weeks' repeated administration of AS2444697 (0.3
179829Acecainide HCl34118-92-898.0%
Acecainide, also known as N-acetylprocainamide and ASL 601, is the N-acetylated metab
179816ASC-J952328-98-098.0%
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17987AMG-0091027847-67-198.0%
AMG 009 is an orally active, small molecule CRTH2 (chemoattractant receptor-homologou
17816035-amino-2-fluoro-4-methylbenzonitrile1426136-04-098.0% 
5-amino-2-fluoro-4-methylbenzonitrile 
17816022-azaspiro[3.5]nonan-7-ol hydrochloride1434141-67-996.0% 
2-azaspiro[3.5]nonan-7-ol hydrochloride
178141Abemaciclib ( LY2835219)1231929-97-798.0% 
Abemaciclib, also known as LY2835219, is orally available cyclin-dependent kinase (CD
178910AZD32641609281-86-898.0% 
AZD3264 is a novel and small molecule IKK2 inhibitor.IKK2 serves as a protein subunit
178816A-9714321240308-45-598.0% 
A‑971432 is highly selective for S1P5 and has excellent plasma and CNS exposure aft
20178812A-11654421221443-94-298.0% 
A-1165442 is a temperature-neutral transient receptor potential vanilloid-1 (TRPV1) a
20178710AZD42052091134-35-798.0% 
AZD4205 is a highly potent JAK1-selective kinase inhibitor with excellent preclinical
77821ACY-7751375466-18-498.0% by HPLC 
ACY-775 is a potent and selective HDAC6 inhbiitor. ACY-775 inhibits HDAC6 with low na
1773101AAI-1011001404-83-698.0% 
AAI101(AAI-101) is a novel extended-spectrum -lactamase inhibitor.The combination of
17030105AV-412 Tosylate451493-31-598% 
AV-412, also known as MP-412, is a second-generation, orally bioavailable dual kinase
17022812AZD-75941196509-60-098% 
AZD-7594, also known as AZ13189620, is an inhaled selective glucocorticoid receptor (
17022801ABT888912445-05-798% 
Veliparib (ABT-888) is a potent inhibitor of PARP1 and PARP2 with Ki of 5.2 nM and 2.
17022710AZD38391227163-56-598% 
AZD3839 is a potent and selective BACE1 inhibitor. AZD3839 is clinical candidate for
17022404A-12104771668553-26-198% 
A-1210477 is a potent and selective MCL-1 inhibitor. A-1210477 induces the hallmarks
17022301Apatinib811803-05-198% 
Apatinib is an orally bioavailable, selective VEGFR2 inhibitor with IC50 of 1 nM.
17021407Amikacin sulfate39831-55-598% 
Amikacin sulfate(BAY416651 sulfate) is a semi-synthetic aminoglycoside antibiotic der
17021406AFN-1252620175-39-598% 
AFN-1252(Debio 1452) is a potent inhibitor of enoyl-acyl carrier protein reductase (F
17021318AZD3293 (LY3314814)1383982-64-698% 
AZD3293, also known as LY3314814 is an oral beta-secretase 1 cleaving enzyme (BACE) 
17021316APR-246 (PRIMA-1MET)5291-32-798% 
APR-246, also known as PRIMA-1MET, is a small organic molecule that has been shown to
102703AZD-88351620576-64-8≧98.0%
AZD8835 is a potent and selective inhibitor of PI3Kalpha and PI3Kdelata with excellen
17011901AZD6482 (S-isomer)1173900-37-298% 
AZD6482 is a potent, selective and ATP competitive PI3K inhibitor (IC(50) 0.01 μm).
170113027ACC21472624-85-398% 
7ACC2 is a potent MCT inhibitor. Monocarboxylate transporters (MCTs) catalyze the pro
16122865AZD-5597924641-59-898% 
AZD-5597 is potent CDK inhibitor with in vitro anti-proliferative effects against a r
16122864AZD-5069878385-84-398% 
AZD-5069 is a potent and selective CXCR2 antagonist with the potential to inhibit neu
16122863AZD-24611174043-16-398% 
AZD2461 is a novel and potent PARP inhibitor with lower affinity to P-glycoprotein. A