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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
2062321tert-Butyl 2-((tosyloxy)methyl)morpholine-4-carboxylate130546-33-798% Min.
2062318 tert-butyl 3-bromo-5-chloro-2-fluorophenyl-carbamate1269232-94-198% Min.
2062310tert-butyl N-(4-bromo-2-methoxyphenyl)carbamate262433-01-298% Min.
2062302Thiazole-5-carboxylic acid14527-41-498% Min.
2062301tert-butyl N-[[4-[(Z)-C-chloro-N-hydroxycarbonimidoyl]phenyl]methyl]-N-methylcarbamate1402390-77-596% Min.
2062035tert-butyl 4-[[6-[2-(quinoxaline-2-carbonylamino)phenyl]imidazo[2,1-b][1,3]thiazol-3-yl]methyl]piperazine-1-carboxylate925436-46-096% Min.
2062034tert-Butyl 4-(1-oxoisoindolin-2-yl-methyl)piperidine-1-carboxylate359629-19-998% Min.
20620244,4,5,5-tetramethyl-2-(4-propan-2-ylsulfonylphenyl)-1,3,2-dioxaborolane1256359-13-396% Min.
20620112,3,5-Tri-O-benzyl-D-ribonolactone55094-52-596% Min.
2061704Tafenoquine-d3 succinate1133378-83-298% Min.
Tafenoquine-d3 is a trideuerium-labeled Tafenoquine derivative. Tafenoquine, also kno
2061501TLR4-C3440592-88-998% Min.
TLR4-C34 is a TLR4 inhibitor that inhibits TLR4 signaling in enterocytes and macropha
2061311TH2572244678-29-198% Min.
TH257 is a Potent and selective allosteric LIMK 1/2 inhibitor.
2061303TH-263313520-94-498% Min.
TH-263 is an inactive analog control for the type III allosteric LIM-kinase (LIMK) in
S-2041582,4,6-tris(4-phenylphenyl)-1,3,5-triazine31274-51-898% Min.
S-203041[4-(2,2,2-trifluoroethoxy)phenyl]boronic acid886536-37-495%
g scale to Kg scale may be provided.
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