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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
2041503TVB-366498% Min.
TVB-3664 is a FASN inhibitor which significantly reduces tubulin palmitoylation and m
193184TD-1062250288-69-6>98%
TD-106 is a cereblon (CRBN) modulator, which can be used for targeted protein degrada
193183Tafamidis meglumine 951395-08-7>98%
Tafamidis meglumine , also known as Fx-1006 or PF-06291826, is a drug for the amelior
193182Tafamidis 594839-88-0>98%
Tafamidis, Tafamidis, also known as Fx-1006 or PF-06291826, is a drug for the amelior
193135TH2871609960-30-6>98%
TH287 is a potent inhibitor of human 7,8-Dihydro-8-oxoguaninetriphosphatase MTH1 (NUD
193112Tinostamustine HCl1793059-58-1>98%
Tinostamustine, also known as EDO-S101, is an alkylatlng histone-deacetylase inhibito
19374Telithromycin191114-48-4>98%
Telithromycin, also known as HMR-3647 and RU-66647, is a semi-synthetic erythromycin
192273TH342196203-96-8>98%
TH34 is a potent HDAC6/8/10 inhibitor. TH34 induces DNA damage-mediated cell death in
192252THZ21604810-84-5>98%
THZ2, an analog of THZ1, with the potential to treat Triple-negative breast cancer (T
192145Tegatrabetan1227637-23-1>98%
Tegatrabetan, also known as Tegavivint and BC2059, is an orally bioavailable and pote
192144Telratolimod1359993-59-1>98%
Telratolimod, also known as 3M-052 or MEDI-9197, is a toll-like receptor 7 (TLR-7) an
191286TAS-​1161260533-36-5>98%
TAS-116 is a potent and selective inhibitor of heat shock protein 90 (Hsp90) subtypes
191254Tamibarotene94497-51-5>98%
Tamibarotene, also known as SY-1425, is an orally active, synthetic retinoid, develop
191123Tafenoquine succinate106635-81-8≧98.0%
Tafenoquine is being investigated as a potential treatment for malaria, as well as fo
191122Tafenoquine ( WR 238605 )106635-80-7≧98.0%
Tafenoquine is being investigated as a potential treatment for malaria, as well as fo
1812282TP0463518 1558021-37-0>98%
TP0463518 is a novel, highly potent HIF prolyl hydroxylase (PHD) inhibitor. TP0463518
1812133Thiamet G1009816-48-1>98%
Thiamet G is a potent and selective inhibitor of O-GlcNAcase.
181252Talmapimod HCl309915-12-6>98%
Talmapimod, also known as SCIO-469, is an orally bioavailable, small-molecule, p38 mi
181232TG4-1551164462-05-8>98%
TG4-155 is a brain penetrant EP2 antagonist (KB = 2.4 nM) that is over 1000-fold less
181231Tebanicline HCl203564-54-9>98%
Tebanicline, also known as ABT-594 and Ebanicline, a potent synthetic nicotinic (non-
1811212Topotecan123948-87-8>98%
Topocecan is a semisynthetic derivative of camptothecin with antineoplastic activity.
1811191TAS-1201448169-71-8>98%
TAS-120 is an orally bioavailable inhibitor of the fibroblast growth factor receptor
1811161Tulrampator ( CX-1632 )1038984-31-4≧98.0%
Tulrampator, also known as S-47445 and CX-1632, is a positive allosteric modulator (P
1811122Thiazovivin1226056-71-8>98%
Thiazovivin is a selective, cell-permeable small molecule that inhibits ROCK activity
1811021TH 12171862212-48-3>98%
TH 1217 is a potent dCTP pyrophosphatase 1 inhibitor.
18831TW-37877877-35-5>98%
TW-37 is a small-molecule inhibitor of Bcl-2 family proteins, inhibited cell growth a
187202TAK-715303162-79-0>98%
TAK-715 is a potent p38 MAPK inhibitor. which displays potent inhibitory activity and
18762TAK-9601137868-52-0>98%
TAK-960 is an orally available PLK1 inhibitor with potential antineoplastic activity.
186235Theliatinib1353644-70-8>98%
Theliatinib, also known as HMPL-309, is a novel small molecule, epidermal growth fact
186233Tucidinostat1616493-44-7>98%
Tucidinostat is a benzamide type inhibitor of histone deacetylase (HDAC) isoenzymes 1