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TH 1217, also known as ZINC1775962367, is a potent and selective dCTPase pyrophosphatase 1 (dCTPase) inhibitor, with...
TH-162, also known as (R)-PIA and Adenosine, N-(1-methyl-2-phenylethyl)-, (R)- is an A1 adenosine receptor...
TH1760 is a novel inhibitor against the NUDIX hydrolase NUDT15, sensitizing cells to 6-thioguanine through enhanced...
TH-2120, also known as Sodium ionophore III, is a ionophore. Ionophore is suitable for the assay of sodium activity...
TH-237A is a novel neuroprotective agent, which possess protective properties against β-amyloid (Aβ)-induced...
TH257 is a Potent and selective allosteric LIMK 1/2 inhibitor.
TH-263 is an inactive analog control for the type III allosteric LIM-kinase (LIMK) inhibitors TH-257, TH-255 and...
TH287 is a potent inhibitor of human 7,8-Dihydro-8-oxoguaninetriphosphatase MTH1 (NUDT1) with an IC50 value of 5 nM...
TH34 is a potent HDAC6/8/10 inhibitor. TH34 induces DNA damage-mediated cell death in human high-grade neuroblastoma...
TH 5487 is a selective 8-oxoguanine DNA glycosylase 1 (OGG1) inhibitor.
TH588 is a potent inhibitor of human 7,8-Dihydro-8-oxoguaninetriphosphatase MTH1 (NUDT1) with an IC50 value of 5 nM...
TH 588 hydrochloride
CAS#: 1640282-30-9 (HCl);
TH588 HCl is a potent inhibitor of human 7,8-Dihydro-8-oxoguaninetriphosphatase MTH1 (NUDT1) with an IC50 value of 5...
Thailanstatin A, also known as TST-A, is a potent antiproliferative agent, which was isolated from the fermentation...
Thalidomide is a synthetic derivative of glutamic acid (alpha-phthalimido-glutarimide) with teratogenic,...
Thalidomide 5'-amine-alkylC10-amine is a functionalized cereblon ligand for PROTAC® research and development;...
Thalidomide 5'-amine-alkylC8-amine is a functionalized cereblon ligand for PROTAC® research and development;...
Thalidomide-5-(C6-amine) is a PROTAC building block that contains an E3 ligase ligand substituted with a terminal...
Thalidomide-5-(PEG2-acid) is a PROTAC building block that contains an E3 ligase ligand substituted with carboxylic...
Thalidomide-5-(PEG2-amine) is a PROTAC building block that contains an E3 ligase ligand substituted with a terminal...
Thalidomide-5-(PEG4-acid) is a PROTAC building block that contains an E3 ligase ligand substituted with carboxylic...
Thalidomide-5-(PEG4-amine) is a PROTAC building block that contains an E3 ligase ligand substituted with a terminal...
Thalidomide-Acid is a linker of Thalidomide which is commonly used as a precursor to PROTAC that hijacks cereblon as...
Thalidomide-O-acetamido-C4-amine HCl salt
Thalidomide-O-acetamido-C4-amine HCl salt is comprised of a Thalidomide based cereblon ligand and a ligand-linker...
Thalidomide-O-amido-PEG4-azide is a PROTAC linker that is reactive with alkyne or DBCO, BCN attached molecule via...
Thalidomide-O-Hexyl-Acid is an E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon...