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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
92206Pyrrolidin-1-yl-acetic acid hydrochloride6628-74-698% 
Coming soon!
91806phenyl 2-(benzyloxy)-3-(dibenzylamino)-5-fluoro-6-methylbenzoate1253799-29-998% 
Coming soon!
914093-Piperazinobenzisothiazole Hydrochloride144010-02-698% 
The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3
914083-(1-Piperazinyl)-1,2-Benzisothiazole87691-87-098% 
The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3
907093-(4-phenoxyphenyl)propanoic acid20062-91-398% 
Coming soon!
82406PFI-4900305-37-598% 
PFI-4 is a potent and selective BRPF1 bromodomain inhibitor (IC50 = 80 nM). Exhibits
81821Piperazin-2-ylmethanol dihydrochloride122323-87-998% 
Coming soon!
81817Piperazine-2-Carboxylic Acid Methyl Ester Dihydrochloride122323-88-098% 
Coming soon!
81814Piperazine-2-carboxylic acid dihydrochloride3022-15-998% 
Coming soon!
81302Pimecrolimus137071-32-098% 
Pimecrolimus is an immunophilin ligand, which binds specifically to the cytosolic rec
81301Pitavastatin Calcium147526-32-798% 
Pitavastatin is a member of the blood cholesterol lowering medication class of statin
73109PKI-5871197160-78-397% 
PKI-587 is a potent inhibitor to PI3K-, PI3K-, and mTOR (FRAP) with IC50 of 0.4 nM, 5
52824PFK-0154382-63-298% 
PFK-015 is an effective inhibitor of PFKFB3 with IC50 of 110 nM (recombinant PFKFB3)
52817Pramiracetam68497-62-198% 
Pramiracetam is a nootropic drug derived from piracetam, and is more potent. Pramirac
52816PF-573228869288-64-298% 
PF-573228 is a potent and selective FAK inhibitor with IC50 of 4 nM for inhibiton of
52815Paromomycin Sulfate1263-89-498% 
Paromomycin Sulfate is an aminoglycoside antibiotics inhibiting protein synthesis in
52756PLX647873786-09-598% 
PLX647 is a highly specific dual FMS/KIT kinase inhibitor with IC50 of 28/16 nM respe
52753Pexidartinib1029044-16-398% 
pexidartinib is acapsule formulation containing a small-molecule receptor tyrosine ki
52740PF-5431415562-82-198% 
PF-543 is a novel cell-permeant inhibitor of SphK1 with a Ki of 3.6 nM, PF-543 is sph
52718PSI-79771190307-88-098% 
PSI-7977(sofosbuvir) is an investigational nucleotide analog for treatment of chronic
52701Pirfenidone53179-13-898% 
Pirfenidone(AMR69) is an inhibitor for TGF- production and TGF- stimulated collagen p
52634Poziotinib1092364-38-998% 
Poziotinib(NOV120101; HM781-36B) is an irreversible Pan-HER inhibitor with IC50s of 3
52631PF-47086711255517-76-098% 
PF-4708671 is a novel cell-permeable inhibitor of S6K1 (p70 ribosomal S6 kinase 1), w
52613Perifosine157716-52-498% 
Perifosine (KRX-0401; D-21266; NSC 639966) is a novel Akt inhibitor with IC50 of 4.7
52603Plinabulin714272-27-298% 
Plinabulin (NPI-2358) is a vascular disrupting agents (VDA) against tubulin-depolymer
52592PLX-4720918505-84-798% 
PLX 4720 is a potent and selective inhibitor of B-RafV600E(IC50=13 nM) and c-Raf-1Y34
52591Palomid 529914913-88-598% 
Palomid 529 (P529) is a novel potent inhibitor of both the mTORC1 and mTORC2 complexe
52583PHT-4271191951-57-198% 
PHT-427 is a dual Akt and PDPK1 inhibitor (high affinity binding for the PH domains o
52564Purvalanol A212844-53-698% 
Purvalanol A(NG-60) is a potent, cell-permeable, and selective inhibitor of cyclin-de
52560PI3K-IN-11349796-36-698% 
PI3K-IN-1 is a potent inhibitor of PI3K, more information can be found in patent WO20