HMS-101

Modify Date: 2025-08-25 19:16:35

HMS-101 Structure
HMS-101 structure
Common Name HMS-101
CAS Number 1070690-06-0 Molecular Weight 305.433
Density 1.1±0.1 g/cm3 Boiling Point 395.2±42.0 °C at 760 mmHg
Molecular Formula C18H28FN3 Melting Point N/A
MSDS N/A Flash Point 192.8±27.9 °C

 Use of HMS-101


HMS-101 (HMS101) is a potent, selective mutant IDH1 inhibitor, the IC50 is significantly lower in mouse bone marrow cells transduced with IDH1mut compared with IDH1wt (1 uM vs 12 uM, respectively); binds to the isocitrate-binding pocket of mutant IDH1, significantly reduces intracellular R-2HG levels in vitro HoxA9+IDH1mut cells at 10 uM; induces apoptosis in IDH1mut cells, markedly reduces phospho-ERK1/2 and the ratio of phospho-ERK/total-ERK, inhibits human AML cell growth.

 Names

Name 2-{2-[3-(4-Fluorophenyl)-1-pyrrolidinyl]ethyl}-1,4-dimethylpiperazine
Synonym More Synonyms

 HMS-101 Biological Activity

Description HMS-101 (HMS101) is a potent, selective mutant IDH1 inhibitor, the IC50 is significantly lower in mouse bone marrow cells transduced with IDH1mut compared with IDH1wt (1 uM vs 12 uM, respectively); binds to the isocitrate-binding pocket of mutant IDH1, significantly reduces intracellular R-2HG levels in vitro HoxA9+IDH1mut cells at 10 uM; induces apoptosis in IDH1mut cells, markedly reduces phospho-ERK1/2 and the ratio of phospho-ERK/total-ERK, inhibits human AML cell growth.
References References 1. Chaturvedi A, et al. Blood. 2013 Oct 17;122(16):2877-87. View Related Products by Target Isocitrate Dehydrogenase (IDH)

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 395.2±42.0 °C at 760 mmHg
Molecular Formula C18H28FN3
Molecular Weight 305.433
Flash Point 192.8±27.9 °C
Exact Mass 305.226715
LogP 1.75
Vapour Pressure 0.0±0.9 mmHg at 25°C
Index of Refraction 1.524

 Synonyms

Piperazine, 2-[2-[3-(4-fluorophenyl)-1-pyrrolidinyl]ethyl]-1,4-dimethyl-
2-{2-[3-(4-Fluorophenyl)-1-pyrrolidinyl]ethyl}-1,4-dimethylpiperazine
MFCD30726281
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