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Catalog NoChemical NameCAS NumberPurityChemical Structure
175161PF-067477751776112-90-398% by HNMR/HPLC 
PF-06747775(PF06747775;CAS 1776112-90-3) is an orally available inhibitor of the epid
17031017PF-049952741331782-27-498% 
PF-04995274 is a 5-HT4 receptor partial agonist. It thought to act centrally as a pro
17031016Pilsicainide HCl88069-49-298% 
Pilsicainide, also known as SUN 1165, is a drug used clinically in Japan to treat car
17031011PNU-74654113906-27-798% 
PNU-75654 disrupts the Wnt signaling pathway via inhibition of the interaction (KD5
17031005PACAP 1-27127317-03-798% 
Pituitary adenylate cyclase activating polypeptide (PACAP 1-27) is a potent PACAP re
17030918Ponesimod854107-55-498% 
Ponesimod, also known as ACT-128800, is a potent, and orally active selective S1P(1)
17030916Pimobendan74150-27-998% 
Pimobendan is a veterinary medication. Pimobendan is both a calcium sensitizer and a
17030915PFK-1581462249-75-798% 
PFK-158, also known as ACT-PFK-158, is an inhibitor of 6-phosphofructo-2-kinase/fruct
17030914PH-797804586379-66-098% 
PH-797804 is a potent and selectiove inhibitor of p38 mitogen-activated protein (MAP)
17030913PIK-75372196-67-398% 
PIK-75 was developed as part of a PI 3-kinase drug discovery program. PIK75 attenuate
17030912PF-050897711235403-62-998% 
PF-05089771 is a Selective Nav1.7 Inhibitor (IC50 = 11 nM) that interacts with the vo
17030716PF-CBP198% 
PF-CBP1, also known as PF-06670910, is potent and highly-selective inhibitor of the b
17030708Piperoxan HCl135-87-598% 
Piperoxan, also known as benodaine, is a drug which was the very first antihistamine
17030704PFI-11403764-72-698% 
PFI-1 is a potent and highly selective protein interaction Inhibitor, which targets B
17030702Pirmenol68252-19-798% 
Pirmenol is an antiarrhythmic agent. Pirmenol inhibits muscarinic acetylcholine recep
17030607Ponatinib HCl1114544-31-898% 
Ponatinib, also known as AP24534 is an oral drug for the treatment of chronic myeloid
17030304PD-161570192705-80-998% 
PD-161570 is a selective FGFR inhibitor (IC50 values are 40, 262 and 3700 nM for FGFR
17030201PF-062733401402438-74-798% 
PF-06273340 is a Potent, Selective, and Peripherally Restricted Pan-Trk Inhibitor wit
17030115PF-83801144035-53-998% 
PF-8380 is a potent autotaxin inhibitor with an IC(50) of 2.8 nM in isolated enzyme a
17030111Pleconaril153168-05-998% 
Pleconaril is an antiviral drug potentially for the treatment of enterovirus infectio
17022809Panobinostat404950-80-798% 
Panobinostat(LBH-589) is a broad-spectrum HDAC inhibitor; low nanomolar concentration
17022702Pelitinib257933-82-798% 
Pelitinib (EKB-569; WAY-EKB 569) is a potent irreversible EGFR inhibitor with IC50 of
17022402PCI-34051950762-95-598% 
PCI-34051 is a potent, histone deacetylase 8 (HDAC8)-specific inhibitor with >200-fol
17021307Psoralen66-97-798% 
Psoralen is a naturally occurring furocoumarin that intercalates with DNA, inhibiting
16122838P7C3-A201235481-90-998% 
P7C3-A20 is an analogue of P7C3, and is a proneurogenic, neuroprotective agent. P7C3-
16122837P7C3301353-96-898% 
P7C3 is a proneurogenic, neuroprotective agent. P7C3 protects newborn neurons from ap
1612271093PO13309-08-598% 
3PO is a PFKFB3 (6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase) inhibitor. 3PO
161227104Perampanel380917-97-598% 
Perampanel is an orally active, non-competitive, and selective alpha-amino-3-hydroxy-
16122795P5091 (P005091)882257-11-698% 
P5091(P005091) is a selective and potent inhibitor of ubiquitin-specific protease 7 (
16122793PYR-41418805-02-498% 
PYR-41 is the first cell-permeable inhibitor of ubiquitin-activating enzyme E1, with