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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
20504WM 38352229025-70-998% Min.
WM 3835 is a lysine acetyltransferase HBO1 (KAT7) inhibitor. It reduces H3K14ac level
20491WK500B2253985-29-298% Min.
WK500B is a BCL6 inhibitor. WK500B engaged BCL6 inside cells, blocked BCL6 repression
11022WP-1130856243-80-698% Min.
Degrasyn, also known as WP1130, is a small molecule that specifically and rapidly dow
20280WIN54954107355-45-398% Min.
WIN54954 is a broad-spectrum antipicornavirus drug.
12249WAY200070440122-66-798% Min.
WAY200070 is a selective ERβ receptor agonist that displays 68-fold selectivity over
19191WZ-31461214265-56-1>98%
WZ-3146 is a covalent or irreversible pyrimidine-based EGFR inhibitor against EGFR T7
18122525WKS 1350752-07-6>98%
5WKS, also known as ZINC97756584, is a biochemical.
181181WM-1119 2055397-28-7>98%
WM-1119 is a highly potent, selective inhibitor of lysine acetyltransferase KAT6A wit
185710WHI-P97211555-05-4>98%
WHI-P97 is a JAK3 inhibitor.
184315WT1611206731-57-8>98%
WT161 is a novel potent, selective, and bioavailable HDAC6 inhibitor.
17101613WEHI-5391431866-33-9>98%
WEHI-539 is a highly potent and selective BCL-XL inhibitor. The pro-survival BCL-2 fa
1781007WEHI-3451354825-58-398.0% 
WEHI-345 is a potent and selective RIPK2 inhibitor which shows NOD signalling events
17031003Wogonin632-85-998% 
Wogonin, a natural and biologically-active flavonoid found in plants, has been report
17030203WZ40031214265-58-398% 
WZ4003 is a selective inhibitors of the LKB1-tumour-suppressor-activated NUAK kinases
170213211400W214358-33-598% 
1400W is a slow, tight binding, and highly selective inhibitor ofinducible nitric-oxi
16122847WWL70947669-91-2≧98.0%
WWL70 is selective ABHD6 inhibitor, and it has shown anti-inflammatory and neuroprote
16122846Wnt-C591243243-89-198% 
Wnt-C59 is a potent porcupine (PORCN) inhibitor. Wnt-C59 inhibits PORCN activity in v
16122845WDR5-0103890190-22-498% 
WDR5-0103 is a small molecule that binds a peptide-binding pocket on WDR5 (Kd = 450 n
16122786Wnt agonist 1853220-52-798% 
Wnt agonist 1 is a cell permeable Wnt signaling pathway activator, which induces -cat
16122747WS31421227-52-298% 
WS3 is a cell proliferation inducer via modulation of Erb3 binding protein-1 (EBP1)
6111509WNK4632012607-27-998% 
WNK463 is a pan-WNK-kinase inhibitor. It potently inhibits the in vitro kinase activi
6111405WEHI-539 hydrochloride98% 
WEHI-539, has high affinity (subnanomolar) and selectivity for BCL-XL and potently ki
611927WHI-P180 hydrochloride153437-55-998% 
WHI-P180 hydrochloride is a potent EGFR and Cdk2 inhibitors with IC50 of 4.0 and 1.0
161009014WAY-6001062159-35-698% by HPLC 
WAY-600 is a potent, ATP-competitive and selective inhibitor of mTOR with IC50 of 9 n
1610912WYE-6871062161-90-398% by HPLC 
WYE-687 is a potent and ATP-competitive and selective inhibitor of mTOR with IC50 of
161009008WYE-1251321144068-46-198% by HPLC 
WYE-132 inhibited mTORC1 and mTORC2 in diverse cancer models in vitro and in vivo. Im
1610101WYE-3541062169-56-598% by HPLC 
WYE-354 is a potent cell-permeable inhibitor of mTOR (IC50 = 4.3 nM) which blocks sig
160926005Wortmannin19545-26-798% by HPLC 
It has an in vitro inhibitory concentration (IC50) of around 5 nM, making it a more p
31002WAY-181187554403-49-598% 
WAY-181187 is a potent and selective 5-HT6 receptor agonist with Ki value of 2.2 nM.
122825Wy-1464350892-23-498% 
Wy-14643 is a moderate agonist of PPAR and PPAR with IC50 of 36.5 M and 53.7 M, respe