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Catalog NoChemical NameCAS NumberPurityChemical Structure
61726Ensifentrine ( RPL554 )1884461-72-6≧98.0%
Ensifentrine (RPL554) is an investigational, first-in-class, inhaled dual inhibitor o
2073104Enarodustat ( JTZ-951 )1262132-81-998% Min.
Enarodustat ( JTZ-951 ) is an orally-active HIF-PH inhibitor with an EC50 of 0.22 Μm
2071554Empesertib1443763-60-798% Min.
Empesertib, also known as BAY1161909, is an orally bioavailable, selective inhibitor
2071537EIDD-19313258-02-498% Min.
EIDD-1931 is a promising COVID-19 inhibitor. EIDD-1931 has broad spectrum antiviral a
2062030ethyl 2-(2-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)acetate2107880-93-198% Min.
2061703Ethacrynic acid58-54-898% Min.
Etharcrynic Acid is a compound that inhibits symport of sodium, potassium, and chlori
2061302EB-3D1839150-63-8(溴化物98% Min.
EB-3D is a novel potent and selective choline kinase ChoKα inhibitor. EB-3D Induces
2052801Elexacaftor2216712-66-098% Min.
Elexacaftor, also known as VX-445 and WHO 11180, is a next-generation cystic fibrosis
2051508EC-50261809885-32-298% Min.
EC5026, also known as BPN-19186, is a first-in-class, potent and orally active solubl
1843212Ensartinib hydrochloride2137030-98-798% Min.
Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k
112594Evenamide HCl1092977-06-498% Min.
Evenamide HCl ( CAS 1092977-06-4) ,a sodium channel blocker, shows efficacy in a broa
112593Evenamide1092977-61-198% Min.
venamide is a sodium and/or calcium channel modulator. Evenamide may be potentia usef
95071ethyl 2-acetyl-4-bromobenzoate182567-89-1>98%
ethyl 2-acetyl-4-bromobenzoate;2-ACETYL-4-BROMOBENZOIC ACID ETHYL ESTER
19318Ertapenem 153832-46-3>98%
Ertapenem is a parenteral carbapenem that is highly resistant to inactivation by a wi
192182Eprosartan 133040-01-4>98%
Eprosartan is a competitive and reversible angiotensin II receptor antagonist used fo
192153EX-229 free acid1219739-36-2>98%
EX-229, also known as AMPK Activator 991, is a novel AMPK activator, increasing AMPK
19121Elacridar HCl143851-98-3>98%
Elacridar, also known as GF120918A, is a P-glycoprotein (P-gp) inhibitor, and has bee
1812293E7820289483-69-8>98%
E7820 is a small molecule and aromatic sulfonamide derivative with potential antiangi
1810253EMD6386831181770-72-8>98%
EMD638683 is a potent inhibitor of SGK1 with an IC50 value of 3 μM.
1810231E2012870843-42-8>98%
E2012 is a γ-secretase modulator (GSM).
1810165EBI-25112098546-05-3>98%
EBI-2511 is a Highly Potent and Orally Active EZH2 Inhibitor for the Treatment of Non
186293Entasobulin501921-61-5>98%
Entasobulin is a β-tubulin polymerization inhibitor with potential anticancer activi
186292Epothilone D189453-10-9>98%
Epothilone D is a natural polyketide compound isolated from the myxobacterium Sorangi
186272EZM23021628830-21-6>98%
EZM2302 is a potent, selective, and orally available arginine methyltransferase CARM1
186271Exatecan mesylate169869-90-3>98%
Exatecan, also known as DX 8951, is semisynthetic, water-soluble camptothecin derivat
186213Efinaconazole164650-44-6>98%
Efinaconazole is a triazole antifungal. It is approved for use in Canada and the USA
186157Erteberel533884-09-2>98%
Erteberel, also known as LY500307, is a selective estrogen receptor beta (ERβ) agoni
18671Edonerpic maleate519187-97-4>98%
Edonerpic, also known as T-817, is a neuroprotectant.
184124Endoxifen E-isomer HCl1197194-61-8>98%
Endoxifen E-isomer is a tamoxifen metabolite and potent Selective Estrogen Response M
184321Ensartinib ( X396 )1370651-20-9>98%
Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k