Mavoglurant (CHEM100435)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-05 11:40:25 UTC | ||||||||
| Update Date | 2026-08-20 03:45:54 UTC | ||||||||
| Accession Number | CHEM100435 | ||||||||
| Identification | |||||||||
| Common Name | Mavoglurant | ||||||||
| Class | Small Molecule | ||||||||
| Description | Mavoglurant is an organic compound with the formula C19H23NO3 and an average molecular weight of 313.40 g/mol. Mavoglurant belongs to the indoles and derivatives, a class of organoheterocyclic compounds within the organic compounds. Regarding its pharmacological activity, the compound is recorded as a modulator of the protein target Metabotropic glutamate receptor 5 (GRM5). | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C19H23NO3 | ||||||||
| Average Molecular Mass | 313.397 g/mol | ||||||||
| Monoisotopic Mass | 313.168 g/mol | ||||||||
| CAS Registry Number | 543906-09-8 | ||||||||
| IUPAC Name | methyl (3aR,4S,7aR)-4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-octahydro-1H-indole-1-carboxylate | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | COC(=O)N1CC[C@@H]2[C@H]1CCC[C@@]2(O)C#CC1=CC=CC(C)=C1 | ||||||||
| InChI Identifier | InChI=1S/C19H23NO3/c1-14-5-3-6-15(13-14)8-11-19(22)10-4-7-17-16(19)9-12-20(17)18(21)23-2/h3,5-6,13,16-17,22H,4,7,9-10,12H2,1-2H3/t16-,17-,19-/m1/s1 | ||||||||
| InChI Key | ZFPZEYHRWGMJCV-ZHALLVOQSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
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| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
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| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
| External Links | |||||||||
| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
