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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
20654Lorundrostat1820940-17-798% Min.
Lorundrostat is an aldosterone synthase inhibitor.
20625LEO-327311353546-86-798% Min.
LEO-32731 is a bioactive chemical.
20588Losmapimod585543-15-398% Min.
Losmapimod, also know as GW856553 or GW856553X or GSK-AHAB, is a drug developed by Gl
20577LY35223482568608-48-898% Min.
20551Lin281632108825-65-698% Min.
Lin28 1632, is a RNA binding protein Lin28 inhibitor. Lin281632 promotes mESC differe
20531LUNA18unknown98% Min.
LUNA18 is a N-alkyl-rich cyclic peptide
20477LQZ-7I195822-23-298% Min.
LQZ-7I is a malarial protease PfSUB1 inhibitor. LQZ-7I showed significantly improved
20461LSN24633591401031-52-498% Min.
LSN2463359 is a novel positive allosteric modulators of the mGlu₅ receptor.
20438LFM-A13244240-24-298% Min.
LFM-A13 is a potent and selective inhibitor of Bruton's tyrosine kinase (BTK). LF
20266Linzagolix935283-04-8≧98.0%
Linzagolix is a novel, orally administered GnRH receptor antagonist that potentially
21244LY-34750702375815-63-598% Min.
LY-3475070 is a potent and selective CD73 Inhibitor with IC50 of 28 nM. LY3475070 Alo
210507LP-261915412-67-8≧98.0%
LP-261 is a novel tubulin targeting anticancer agent that binds at the colchicine sit
21225LM11A-31 HCl1243259-19-998% Min.
20113001LVN84663103784-66-398% Min.
LVN84663 is a useful reagent for determination of blood coagulating protease. It was
2091908LUN4251847142-51-898% Min.
LUN42518, also known as Phentolamine Analogue 1, is an analogue of phentolamine. Phen
2073106Lerociclib HCl (G1T38 HCl)2097938-59-3≧98.0%
Lerociclib HCl (G1T38)is a novel, selective,differentiated oral CDK4/6 inhibitor with
2071555Lobaplatin135558-11-198% Min.
Lobaplatin (D-19466) is a diastereometric mixture of platinum(II) complexes containin
2071524Lixivaptan168079-32-198% Min.
Lixivaptan, laso known as CRTX-080; VPA-985; WAY-VPA-985, is a potent, orally active,
2071505LAU1592055050-87-698% Min.
LAU159 is a potent modulator of α6β3γ2 GABAA receptor.
2071502Lificiguat170632-47-098% Min.
Lificiguat, also known as YC-1, is a inhibitor of Hypoxia-inducible factor-1alpha (HI
20732Lanraplenib1800046-95-098%
Lanraplenib (GS-9876) is a highly selective and orally active SYK inhibitor in develo
2061309Linperlisib free base1702816-75-898% Min.
Linperlisib, also known as YY-20394 and PI3Kδ-IN-2, is a potent and selective PI3Kδ
2061307 L006235294623-49-798% Min.
L006235 is a potent, reversible cathepsin K inhibitor (IC50 = 0.25 nM) that displays
2051510LML-1341542135-76-198%
LML134 is an orally active and high selective Histamine 3 receptor (H3R) inverse agon
2042701LUT-0142274819-46-298% Min.
LUT-014 is a B-Raf Inhibitor. Leveraging the paradoxical effect of B-Raf Inhibitors,
2041502LSZ1022135600-76-798% Min.
LSZ102 is a potent ERα antagonist and degrader. LSZ102 showed ERα degradation IC50
204502LUN425891848242-58-998% Min.
LUN42589, also known as PI3K/mTOR Inhibitor-2, is a potent dual pan-PI3K/mTOR inhibit
204302Lerociclib1628256-23-4 (free base)98%
Lerociclib , also known as G1T38, is an oral, potent and selective CDK4/6 inhibitor f
6111904Lemborexant (E-2006)1369764-02-298% Min.
Lemborexant(CAS 1369764-02-2)is a novel investigational small molecule that inhib
193262LY27941932173037-97-1>98%
LY2794193 is a highly potent and selective mGlu3 receptor agonist.