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YM-202074 sesquifumarate salt hydrate_Molecular_structure_CAS_299900-84-8(anhydrous))
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YM-202074 sesquifumarate salt hydrate

Catalog No. Y1271 Name Sigma Aldrich
CAS Number 299900-84-8(anhydrous) Website http://www.sigmaaldrich.com
M. F. C74H100N12O15S3 Telephone 1-800-521-8956
M. W. 1493.8522 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 154474

SYNONYMS

IUPAC name
tris(N-cyclohexyl-11-{[(2-methoxyethyl)(methyl)amino]methyl}-N-methyl-5-thia-2,7-diazatricyclo[6.4.0.02,6]dodeca-1(12),3,6,8,10-pentaene-4-carboxamide) bis(but-2-enedioic acid) hydrate
IUPAC Traditional name
tris(N-cyclohexyl-11-{[(2-methoxyethyl)(methyl)amino]methyl}-N-methyl-5-thia-2,7-diazatricyclo[6.4.0.02,6]dodeca-1(12),3,6,8,10-pentaene-4-carboxamide) bis(butenedioic acid) hydrate
Synonyms
YM 202074
YM202074
N-cyclohexyl-6-{[(2-methoxyethyl)(methyl)amino]methyl}-N-methylthiazolo[3,2-a]benzimidazole-2-carboxamide

DATABASE IDS

MDL Number MFCD16879020
CAS Number 299900-84-8(anhydrous)

PROPERTIES

Empirical Formula (Hill Notation) C22H30N4O2S · 1.5C4H4O4 · xH2O
Purity ≥98% (HPLC)
Apperance white to off-white powder
Solubility DMSO: >20 mg/mL
Solubility H2O: >5 mg/mL
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H301-H319
European Hazard Symbols Toxic Toxic (T)
MSDS Link Download
GHS Precautionary statements P301 + P310-P305 + P351 + P338
RID/ADR UN 2811 6.1/PG 3
Risk Statements 25-36
Safety Statements 26-45
Storage Temperature room temp
Hazard Class 6.1
UN Number 2811
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
YM-202074 is a potent and selective allosteric metabotropic glutamate receptor type 1 (mGluR1) antagonist. It bound an allosteric site of rat mGluR1 with a Ki value of 4.8 nM. It also inhibited the mGluR1-mediated inositol phosphates production in rat cerebellar granule cells with an IC50 value of 8.6 nM, while showing selectivity over mGluR(2-7).
Description (简体中文)
Biochem/physiol Actions
YM-202074 is a potent and selective allosteric metabotropic glutamate receptor type 1 (mGluR1) antagonist. It bound an allosteric site of rat mGluR1 with a Ki value of 4.8 nM. It also inhibited the mGluR1-mediated inositol phosphates production in rat cerebellar granule cells with an IC50 value of 8.6 nM, while showing selectivity over mGluR(2-7).

REFERENCES