Thiorphan (CHEM100582)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-05 11:48:52 UTC | ||||||||
| Update Date | 2026-05-14 18:58:53 UTC | ||||||||
| Accession Number | CHEM100582 | ||||||||
| Identification | |||||||||
| Common Name | Thiorphan | ||||||||
| Class | Small Molecule | ||||||||
| Description | Thiorphan is an organic compound with the formula C12H15NO3S and an average molecular weight of 253.32 g/mol. Thiorphan belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. In terms of its biological activity, it acts as an inhibitor of the protein target Neprilysin (MME). | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C12H15NO3S | ||||||||
| Average Molecular Mass | 253.320 g/mol | ||||||||
| Monoisotopic Mass | 253.077 g/mol | ||||||||
| CAS Registry Number | 76721-89-6 | ||||||||
| IUPAC Name | 2-[(2S)-2-benzyl-3-sulfanylpropanamido]acetic acid | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | OC(=O)CNC(=O)C(CS)CC1=CC=CC=C1 | ||||||||
| InChI Identifier | InChI=1S/C12H15NO3S/c14-11(15)7-13-12(16)10(8-17)6-9-4-2-1-3-5-9/h1-5,10,17H,6-8H2,(H,13,16)(H,14,15)/t10-/m1/s1 | ||||||||
| InChI Key | LJJKNPQAGWVLDQ-SNVBAGLBSA-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 | ||||||||
