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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
19311ML221877636-42-5>98%
ML221 is an antagonist of the apelin (APJ) receptor.
192279Melphalan flufenamide 380449-51-4>98%
Melphalan flufenamide, also known as Melflufen, J-1, or Prodrug J-1, is a melphalan p
192214ML184794572-10-4>98%
CID2440433, also known as ML-184, is a potent synthetic agonist of GPR55 (EC50 = 0.26
192191Mitapivat1260075-17-9>98%
Mitapivat, also known as PKM2 activator 1020 is a PKM2 activator (pyruvate kinase act
192183MK-39031219737-12-8>98%
MK-3903 is a potent and selective AMPK activator (EC50 = 8 nM).
191283Myriocin35891-70-4>98%
Myriocin, also known as antibiotic ISP-1 and thermozymocidin, is an atypical amino ac
191256MA242 TFA1049704-18-8>98%
MA242 is a Dual Inhibitors of MDM2 and NFAT1 for Pancreatic Cancer Therapy. MA242 dec
191252MIK6651799631-75-6>98%
MIK665, also known as S 64315, is an inhibitor of induced myeloid leukemia cell diffe
191211MY 544578351-75-4>98%
MY 5445 is a potential platelet aggregation inhibitor.
19131MRS1706264622-53-9>98%
MRS1706 is a selective adenosine A2B receptor inverse agonist with Ki values of 1.39,
1812296MRS1177183721-13-3>98%
MRS1177 is a bioactive chemical.
1812295MLN-4760305335-31-3>98%
MLN-4760 is an angiotensin-converting (ACE2) inhibitor. In huMNCs, MLN-4760-B detecte
1812254MDK-8384761438-38-4>98%
MDK-8384, also known as ALK inhibitor 2, is a potent and selective ALK inhibitor.
181255Mavacamten1642288-47-8>98%
Mavacamten, also known as SAR-439152 and MYK-461, is a myosin inhibitor potentially f
181251MK-2048 869901-69-9>98%
MK-2048 is a a second-generation HIV-1 integrase inhibitor.
1811282ML 351847163-28-4>98%
ML 351 is a selective 12/15 LOX inhibitor that is active in vivo.
1811261Maropitant147116-67-4>98%
Maropitan, also known as CJ 11972, is a neurokinin (NK1) receptor antagonist.
181152MBQ-1672097938-73-1>98%
MBQ-167 is a potent, dual Rac/Cdc42 inhibitor with IC50 of 103/78 nM, respectively, i
1810301MDK488294164-88-2>98%
MDK4882 also known as PKM2 inhibitor or compound 3k, is a PKM2 inhibitor.
181022MU-3802109805-78-7>98%
MU-380 is a potent and selective CHK1 inhibitor.
1810228MRS1220 183721-15-5>98%
MRS1220 is a potent and highly selective antagonist at the human A3 adenosine recepto
1810174ME03281445251-22-8>98%
ME0328 is an inhibitor of PARP-3 (IC50 = 0.89 μM).
18962MDK-4823 1908414-82-3>98%
MDK-4823, also known as LMPTP inhibitor1; is a potent inhibitor of the low-molecular-
18961MDK-47742036044-77-4>98%
MDK-4774, Porcupine-IN-1, is a Porcupine inhibitor.
18941ML-7921644342-14-2>98%
ML-792 is a potent and selective SAE inhibitor with nanomolar potency in cellular ass
187162ML3271883510-31-3>98%
ML327 is a blocker of MYC. ML327 mediated transcriptional de-repression of E-cadherin
187161MDK36271421373-62-7>98%
MDK3627, also known as Mutant EGFR inhibitor, is a selective and potent Mutated EGFR
18742MLN8054869363-13-3>98%
MLN8054 is an aurora kinase inhibitor MLN8054, which is an orally bioavailable, highl
185284MK-3207957118-49-9>98%
MK-3207 is a potent and orally active calcitonin gene-related peptide receptor antago
185251MI-7731303607-07-9>98%
MI-773 is a novel orally available MDM2 antagonist.