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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
20363methyl 3-bromo-5-formyl-4-hydroxybenzoate706820-79-398% Min.
20362Methyl 3-formyl-4-hydroxybenzoate24589-99-998% Min.
L20346Mycro3944547-46-098% Min.
Mycro3 is an inhibitor of Myc-Max dimerization.
L20331MELK-8a1922153-17-098% Min.
MELK-8a Dihydrochloride is a novel inhibitor of maternal embryonic leucine zipper kin
L20329MTI-311567915-38-198% Min.
MTI-31 is a bioactive chemical.
20325MKC-88661338934-59-098% Min.
MKC-8866, also known as IRE1-IN-8866, is an inhibitor of IRE1 RNase activity. MKC8866
20320MDK-75531700637-55-398% Min.
MDK-7553, also known as CD38 inhibitor 78c and Compound-78c, is a potent CD38 inhibit
204122Mitochonic Acid 51354707-41-798% Min.
Mitochonic Acid 5 is a derivative of the plant hormone indole-3-acetic acid. It has b
20293MK-87221394371-71-198% Min.
MK-8722 is a potent pan-AMPK activator. MK-8722 improves glucose homeostasis but indu
20291MRTX11332621928-55-898% Min.
MRTX1133 is a potent and selective KRAS G12D inhibitor. MRTX1133 targets the KRAS G12
20287ML-SI3891016-02-798% Min.
ML-SI3 is a chemical compound which acts as an "antagonist" (i.e. channel b
20261MYF-01-372416417-65-598% Min.
MYF-01-37 is a novel covalent inhibitor of TEAD targeting Cys380 when incubated with
212563-Methyl-1,2,4-thiadiazole-5-carbohydrazide1375066-73-198% Min.
21245MUN917892144491-78-998% Min.
MUN91789, also known as CPD77, is a potent inhibitor of SARS-CoV-2 main protease. MUN
21243MVN388072379438-80-798% Min.
MVN38807, also known as Y-1, is neuraminidase (NA) inhibitor used in preparation of d
20112602ML008442898-34-298% Min.
ML008, also known as NCGC00092410, is a potent and selective inhibitor of glucocerebr
20111803Mobocertinib free base1847461-43-198% Min.
Mobocertinib, also known as TAK-788 and AP32788, is an investigational TKI with poten
20103003ML3801627138-52-6≧98.0%
ML380 is a highly potent and the first CNS penetrant M5 positive allosteric modulator
2071634METHYL 2,6-DICHLOROBENZOATE14920-87-798% Min.
2071611MAC-545496838810-96-198% Min.
MAC-545496 is potent GraR inhibitor (glycopeptide-resistance-associated protein R). M
2071518MA-02042095128-17-798% Min.
MA-0204 is a highly potent and selective PPARd modulator (PPARδ EC50 = 0.4 nM; PPARa
262325Methyl (R)-2-(Benzyloxy)propionate115458-99-698% Min.
20623204-(2-(6-methylpyridin-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)quinoline-6-carboxylic acid476476-54-798% Min.
20623033-methyl-1-benzofuran-2-carboxylic acid24673-56-198% Min.
20620276-methoxy-4-methyl-1H-quinolin-2-one5342-23-496% Min.
20620193-Methoxythiophene-2-carbaldehyde35134-07-796% Min.
20620183-methoxy-4-(2-morpholinoethoxy)benzoic acid hydrochloride1312941-07-396% Min.
2051511MBX-41322286411-30-998% Min.
MBX-4132 inhibit trans translation by binding to the bacterial ribosome.
2051506ML1881417700-13-098% Min.
ML188 is a Potent Noncovalent Small Molecule Inhibitor of the Severe Acute Respirator
2051504ML2771401242-74-798% Min.
ML277 is a potent activator of KCNQ1 (Kv7.1) channels with >100-fold selectivity v