{"Abbreviation":[],"Aliases":["Zolazepamum","CI 716","Pyrazolo(3,4-e)(1,4)diazepin-7(1H)-one, 4-(2-fluorophenyl)-6,8-dihydro-1,3,8-trimethyl-","Zolasepam","4-(2-fluorophenyl)-1,3,8-trimethyl-1H,6H,7H,8H-pyrazolo(3,4-e)(1,4)diazepin-7-one","Flupyrazapon","Zolazepam-d3","1286480-83-8","4-(2-Fluorophenyl)-1,3,8-trimethyl-6,8-dihydropyrazolo[3,4-e][1,4]diazepin-7(1H)-one","orb1694684","LBC48083","DB11555","4-(2-Fluorophenyl)-6,8-dihydro-1,3,8-trimethylpyrazolo-(3,4-e)(1,4)diazepin-7(1H)-one","Ncgc00522014-01","HY-119146","Q4024647","4-(O-fluorophenyl)-6,8-dihydro-1,3,8-trimethylpyrazolo(3,4-e)(1,4)diazepin-7(1h)-one"],"CAS":"31352-82-6","ChEMBL":"CHEMBL2111144","ChemicalClasses":[],"Chirality":"achiral","Erowid Experience Reports":[],"Esters":[],"European Community (EC) Number":"608-606-2","Formating":[],"HMDB ID":"HMDB0260040","HeavyAtomCount":21,"IUPACName":"4-(2-fluorophenyl)-1,3,8-trimethyl-6H-pyrazolo[3,4-e][1,4]diazepin-7-one","InChI":"InChI=1S/C15H15FN4O/c1-9-13-14(10-6-4-5-7-11(10)16)17-8-12(21)19(2)15(13)20(3)18-9/h4-7H,8H2,1-3H3","InChIKey":"GDSCFOSHSOWNDL-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Agents that alleviate ANXIETY, tension, and ANXIETY DISORDERS, promote sedation, and have a calming effect without affecting clarity of consciousness or neurologic conditions. ADRENERGIC BETA-ANTAGONISTS are commonly used in the symptomatic treatment of anxiety but are not included here. (See all compounds classified as Anti-Anxiety Agents.)","MolecularFormula":"C\u003csub\u003e15\u003c/sub\u003eH\u003csub\u003e15\u003c/sub\u003eFN\u003csub\u003e4\u003c/sub\u003eO","MolecularWeight":"286.30 g/mol","PubChemId":35775,"RefCount":2,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Zolazepam","Name":"Zolazepam","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB11555","Name":"Zolazepam","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/35775","Name":"Zolazepam","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2111144","Name":"Zolazepam","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=31352-82-6","Name":"Zolazepam","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0260040","Name":"Zolazepam","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/G1R474U58U","Name":"Zolazepam","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID30185278","Name":"Zolazepam","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 35775, Zolazepam. Accessed July 27, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/35775\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/35775\u003c/a\u003e"],"SMILES":"CC1=NN(C2=C1C(=NCC(=O)N2C)C3=CC=CC=C3F)C","SaltData":[],"Salts":[],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 65.039 95.8\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#3050f8\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h66v96H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m58.325 59.791-4.728-14.489\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.597 45.302 6.336-8.711M52.664 42.44l5.297-7.283\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m59.933 36.591-3.168 4.356M57.961 35.157l-2.648 3.641\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m59.933 29.427-3.73-5.13M50.324 21.768l-11.255 3.621\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M39.069 25.389v15.24M41.507 27.166v11.686\"/\u003e\u003c/g\u003e\u003cpath d=\"m53.597 45.302-14.528-4.673M39.069 40.629l-11.888 9.55\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m15.652 47.494 11.529 2.685M16.205 45.119l10.374 2.416\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m15.652 47.494 5.764 1.343M16.205 45.119l5.187 1.208\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"M10.561 43.013 5.744 33.009M5.744 33.009l6.604-13.716\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m11.761 20.511-7.425-9.269M13.664 18.986 6.239 9.717\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m4.336 11.242 3.713 4.635M6.239 9.717l3.712 4.635\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m12.348 19.293 11.529-2.685M39.069 25.389l-8.855-7.115M28.051 12.023 30.567.979M27.181 50.179l3.386 14.859\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m45.046 69.532-14.479-4.494M42.983 71.445l-11.79-3.659\"/\u003e\u003c/g\u003e\u003cpath d=\"m45.046 69.532 3.41 14.854\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m37.388 94.745 11.068-10.359M36.752 92l9.014-8.436\"/\u003e\u003c/g\u003e\u003cpath d=\"m37.388 94.745-14.579-4.471\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m19.399 75.421 3.41 14.853M22.091 76.248l2.78 12.108\"/\u003e\u003c/g\u003e\u003cpath d=\"M30.567 65.038 19.399 75.421M19.399 75.421 7.404 71.735M54.831 16.934l3.494-10.707\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M64.479 35.458h-.72l-2.62-4.066h-.03l.03.596q.024.357.024.732v2.738h-.565v-4.899h.714l2.607 4.054h.03l-.018-.327-.024-.477q-.006-.262-.006-.482v-2.768h.578zM55.538 23.165h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.732v2.739h-.565v-4.9h.714l2.608 4.054h.029l-.018-.327-.023-.476q-.006-.262-.006-.482v-2.769h.577zM14.289 49.174h-.721l-2.619-4.066h-.03l.03.596q.024.357.024.732v2.738h-.566v-4.899h.714l2.608 4.054h.03l-.018-.327-.024-.477q-.006-.262-.006-.482v-2.768h.578z\" class=\"atom\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M5.078 7.396q0 .756-.256 1.327-.256.566-.756.881t-1.244.316q-.756 0-1.262-.316-.506-.315-.756-.887Q.56 8.146.56 7.384q0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.863 0q0 .923.387 1.458.393.53 1.22.53.84 0 1.221-.53.387-.535.387-1.458 0-.929-.387-1.453-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.453\" class=\"atom\"/\u003e\u003cpath stroke=\"none\" d=\"M29.122 18.288h-.72l-2.62-4.066h-.029l.029.595q.024.357.024.733v2.738h-.565v-4.899h.714l2.608 4.054h.029l-.018-.328-.023-.476q-.006-.262-.006-.482v-2.768h.577z\" class=\"atom\"/\u003e\u003cpath fill=\"#90e050\" stroke=\"none\" d=\"M4.078 73.395h-.613v-4.9h2.732v.542H4.078v1.738h1.994v.542H4.078z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m59.933 29.427-1.865-2.565M56.203 24.297l1.865 2.565M50.324 21.768l-5.627 1.81M10.561 43.013l-2.409-5.002M23.877 16.608l-5.764 1.342M30.214 18.274l4.428 3.557M28.051 12.023l1.258-5.522\" class=\"hi\"/\u003e\u003cpath stroke=\"#90e050\" d=\"m7.404 71.735 5.998 1.843\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m54.831 16.934 1.747-5.353\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Zolazepam","UNII":"G1R474U58U","Wikipedia":"Zolazepam","XLogP":1.7}