Welcome to Sun-shine chemical
+86-17702719238 sales@sun-shinechem.com

Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
20103002Senaparib1401682-78-7≧98.0%
Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with
2091901SAR 1316751433953-83-398% Min.
SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine
2091205(1S,5R)-1-(3-fluorophenyl)-3-oxabicyclo[3.1.0]hexan-2-one528587-70-498% Min.
2071609SJB2-04363388-44-398% Min.
SJB2-043 is an inhibitor of USP1 target ID1 degradation in leukemic cells.
2071521Spastazoline2351882-11-498% Min.
Spastazoline is a novel inhibitor for aaa+ (atpases associated with diverse cellular
2071510SB 22500218298-32-498% Min.
2071501SCH-23390 maleate87134-87-098% Min.
SCH-23390 hydrochloride is a potent dopamine receptor antagonist (Ki values are 0.2 n
202331((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2-diyl)dimethanol1369767-20-3≧96.0%
The bulk may be provided by custom synthesis.
2062002(S)-4-(((1-Propyl-1H-imidazol-5-yl)methyl)sulfinyl)aniline497223-38-896% Min.
2051514SJ000291942425613-09-898% Min.
SJ000291942 is a bone morphogenic protein (BMP) signaling activator.
2051502Selinexor HClUnknown (HCl)98% Min.
Selinexor, also known as KPT-330, is an orally bioavailable, potent and selective XPO
2051501Selinexor free base1393477-72-9 (free base)98% Min.
Selinexor, also known as KPT-330, is an orally bioavailable, potent and selective XPO
2041504Simurosertib1330782-76-798% Min.
Simurosertib, also known as TAK-931, is an orally bioavailable inhibitor of cell divi
204609SGC2085 free base1821908-48-8 (free base)98% Min.
SGC2085 is a Potent and Selective Coactivator Associated Arginine Methyltransferase 1
204501Segetalin B164991-89-398% Min.
Segetalin B is natural product isolated from Seeds of Vaccaria Segetalis. Segetalin B
112592S26131296280-56-398% Min.
S26131 is a bioactive chemical.
111896SI1131392816-46-498% Min.
SI113 is a specific inhibitor of the Sgk1 kinase activity, counteracting cancer cell
1963013-[(1S)-1-aminoethyl]-8-chloro-2-phenyl-1,2-dihydroisoquinolin-1-one1350643-72-996% Min.
52001Selisistat ( EX-527 )49843-98-3≧98.0%
Selisistatwas the first identified potent and cell permeable SIRT1-specific inhibitor
193261ST-193489416-12-8>98%
ST-193 is a potent broad-spectrum arenavirus inhibitor; inhibits Guanarito, Junin, La
193209SPL-707 2195361-33-0>98%
SPL-707 is the first selective and orally active SPPL2a inhibitor. It shows adequate
193122SHP3942055757-40-7>98%
SHP394 is a potent and orally active SHP2 inhibitor (IC50 = 23 nM) with high lipophil
193113SGC-GAK-1 2226517-76-4>98%
SGC-GAK-1 is a potent and selective GAK kinase probe which targets the ATP-binding si
19314SU 5214186611-04-1>98%
SU 5214 is a modulator of tyrosine kinase signal transduction.
192278Silvestrol697235-38-4>98%
Silvestrol, a member of flavagline family of natural products from the genus of Aglai
192276Selpercatinib2152628-33-4>98%
Selpercatinib is a tyrosine kinase inhibitor with antineoplastic properties.
192215SM16614749-78-9>98%
SM16 is a novel Type I TGF-β signaling inhibitor.
192151SB-674042483313-22-0>98%
SB-674042 is potent and selective OX1R antagonist. SB-674042 binds with high affinity
192147Seclidemstat1423715-37-0>98%
Seclidemstat is an antineoplastic drug candidate.
192146Setafrastat1399715-48-0>98%
Setafrastat is a rotamase inhibitor and vascular endothelial growth factor (VEGF) pro