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￥ 0.00 “17”的搜索结果
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Nitromifene
Catalog No. A20417 -
Simurosertib
Catalog No. A20392 CDC7 inhibitorSimurosertib (TAK-931) is a selective cycle 7 (CDC7) kinase inhibitor, with an IC50<0.3 nM. 了解更多 -
(±)-Zanubrutinib
Catalog No. A20381 Btk inhibitor(±)-Zanubrutinib is a potent, selective and orally available Bruton's tyrosine kinase (Btk) inhibitor. 了解更多 -
Fisogatinib
Catalog No. A20354 FGFR4 inhibitorFisogatinib (BLU-554) is a potent, highly selective and orally active fibroblast growth factor receptor 4 (FGFR4) inhibitor with an IC50 of 5 nM. 了解更多 -
Folcisteine
Catalog No. A20317 -
PDD 00017273
Catalog No. A20305 PARG inhibitorPDD 00017273 is a potent inhibitor of Poly(ADP-ribose) Glycohydrolase (PARG), with an IC50 of 26 nM, and a KD of 1.45 nM. 了解更多 -
Abaperidone
Catalog No. A20286 5-HT2A/dopamine D2 antagonistAbaperidone is a potent antagonist of 5-HT2A?receptor and dopamine D2 receptor with IC50s of 6.2 and 17 nM. 了解更多 -
Linperlisib
Catalog No. A20275 PI3Kδ inhibitorLinperlisib is a potent and selective inhibitor of PI3Kδ extracted from patent WO 2015055071 A1, compound 10; has an IC50 of 6.4 nM. 了解更多 -
Oxamflatin
Catalog No. A20265 HDAC inhibitorOxamflatin (Metacept-3) is a potent HDAC inhibitor with an IC50 of 15.7 nM. 了解更多 -
α-2,3-sialyltransferase-IN-1
Catalog No. A20249 α-2,3-sialyltransferase inhibitorα-2,3-sialyltransferase-IN-1 (Lith-O-Asp analog) is a noncompetitive α-2,3-sialyltransferase inhibitor with an IC50 of 6 μM. 了解更多 -
Palmitodiolein
Catalog No. A20217 Palmitodiolein (Triglyceride POO) is a triacylglycerol which is present in vegetable oils. 了解更多 -
(S,R,S)-AHPC-PEG4-N3
Catalog No. A20214 E3 ligase ligand-linker conjugate(S,R,S)-AHPC-PEG4-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 4-unit PEG linker used in PROTAC technology. 了解更多 -
ALB-127158(a)
Catalog No. A20211 MCH1 receptor antagonistALB-127158(a) is a potent and selective melanin concentrating hormone 1 (MCH1) receptor antagonist. 了解更多 -
Thalidomide-O-amido-C4-NH2
Catalog No. A20184 E3 ligase ligand-linker conjugateThalidomide-O-amido-C4-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. 了解更多 -
Thalidomide-O-amido-C8-NH2
Catalog No. A20174 Thalidomide-O-amido-C8-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. 了解更多 -
MAT2A inhibitor 2
Catalog No. A20171 MAT2A inhibitorMAT2A inhibitor 2 is a methionine adenosyltransferase 2A (MAT2A) inhibitor. 了解更多 -
C-176
Catalog No. A20121 -
Thalidomide-O-amido-C4-NH2 (TFA)
Catalog No. A20120 E3 ligase ligand-linker conjugateThalidomide-O-amido-C4-NH2 TFA (Cereblon Ligand-Linker Conjugates 6 TFA) is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. 了解更多 -
CS-722 Free base
Catalog No. A20119 CS-722 Free base is a synthesized centrally acting muscle relaxant, and has a muscle relaxant activity and depressant effectson the spinal reflex. 了解更多 -
DAAO inhibitor-1
Catalog No. A20117 DAAO inhibitorDAAO inhibitor-1 is a potent D-amino acid oxidase (DAAO) inhibitor with an IC50 of 0.12 μM. 了解更多 -
Branebrutinib
Catalog No. A20043 BTK inhibitorBranebrutinib (BMS-986195) is a highly potent, selective covalent, irreversible inhibitor of Bruton??s tyrosine kinase (BTK), with an IC50 of 0.1 nM. 了解更多
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