{"Abbreviation":["3-CMC"],"Aliases":["3-Chloromethcathinone","Metaclephedrone","3-Cmc","1-Propanone, 1-(3-chlorophenyl)-2-(methylamino)-","1-(3-Chlorophenyl)-2-(methylamino)-1-propanone","1-(3-Chloro-phenyl)-2-methylamino-propan-1-one"],"CAS":"1049677-59-9","ChEMBL":"CHEMBL3298873","ChemicalClasses":["cathinone"],"Chirality":"racemic","Classes":["Stimulant"],"DBI-IGS":["3-CMC","3-CMC"],"Dosing Info":[{"Method":"Insufflated","Tiers":{"Common":{"Entries":0,"Lower":150,"Percentage":0,"Unit":"mg","Upper":150},"Extreme":{"Entries":0,"Lower":200,"Percentage":0,"Unit":"mg","Upper":200},"Heavy":{"Entries":0,"Lower":200,"Percentage":0,"Unit":"mg","Upper":200},"Light":{"Entries":6,"Lower":150,"Percentage":66.7,"Unit":"mg","Upper":150},"Strong":{"Entries":3,"Lower":150,"Percentage":33.3,"Unit":"mg","Upper":200}}},{"Method":"Oral","Tiers":{"Common":{"Entries":2,"Lower":180,"Percentage":25,"Unit":"mg","Upper":280},"Extreme":{"Entries":1,"Lower":353,"Percentage":12.5,"Unit":"mg","Upper":353},"Heavy":{"Entries":1,"Lower":320,"Percentage":12.5,"Unit":"mg","Upper":353},"Light":{"Entries":2,"Lower":180,"Percentage":25,"Unit":"mg","Upper":180},"Strong":{"Entries":2,"Lower":280,"Percentage":25,"Unit":"mg","Upper":320}}},{"Method":"Intrarectal","Tiers":{"Common":{"Entries":1,"Lower":323.7,"Percentage":33.3,"Unit":"mg","Upper":340},"Extreme":{"Entries":1,"Lower":668,"Percentage":33.3,"Unit":"mg","Upper":668},"Heavy":{"Entries":0,"Lower":545,"Percentage":0,"Unit":"mg","Upper":668},"Light":{"Entries":1,"Lower":323.7,"Percentage":33.3,"Unit":"mg","Upper":323.7},"Strong":{"Entries":0,"Lower":340,"Percentage":0,"Unit":"mg","Upper":545}}}],"DurationOfAction":"1 – 4 hours","EliminationHalfLife":"","Esters":[],"Formating":[],"HeavyAtomCount":13,"IUPACName":"1-(3-chlorophenyl)-2-(methylamino)propan-1-one","InChI":"InChI=1S/C10H12ClNO/c1-7(12-2)10(13)8-4-3-5-9(11)6-8/h3-7,12H,1-2H3","InChIKey":"VOEFELLSAAJCHJ-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e12\u003c/sub\u003eClNO","MolecularWeight":"197.66 g/mol","Opticalactivity":"( + / - )","PD":"PD045799","PubChemId":50999285,"Record Description":["Wikipedia|List of designer drugs|Stimulants|Cathinones"],"RefChem":"1054153","RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/3-Chloromethcathinone","Name":"Clophedrone","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q69911605","Name":"Clophedrone","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/50999285","Name":"Clophedrone","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL3298873","Name":"Clophedrone","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD045799","Name":"Clophedrone","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=1049677-59-9","Name":"Clophedrone","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/I2GB1C4TM7","Name":"Clophedrone","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID501014162","Name":"Clophedrone","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 50999285, Clophedrone. Accessed October 14, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/50999285\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/50999285\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Clophedrone. UNII: I2GB1C4TM7. Global Substance Registration System. Accessed October 14, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/I2GB1C4TM7\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/I2GB1C4TM7\u003c/a\u003e"],"SMILES":"CC(C(=O)C1=CC(=CC=C1)Cl)NC","SaltData":[{"AcidCount":1,"Amine":"Clophedrone","AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 121.702 49.848\"\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=\"#1ff01f\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h122v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M71.359 41.181v-15.24M71.359 25.941l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M56.941 19.025V7.002M59.38 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M56.941 7.002v6.011M59.38 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.161 18.321-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m44.962 25.941-13.203-7.628M42.524 27.349l-10.765-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m31.759 18.313-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m18.561 25.933.005 15.248M21 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m18.566 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m31.769 48.81 13.198-7.62M31.769 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m44.962 25.941.005 15.249M18.561 25.933 6.875 19.188M71.359 25.941l10.045-5.799M87.71 20.142l10.045 5.799\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M60.42 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.757 0-1.263-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T58.175.56q.733 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath stroke=\"none\" d=\"M2.906 16.499q-.786 0-1.239.53-.452.524-.452 1.447 0 .91.417 1.446.422.53 1.268.53.321 0 .607-.054.291-.059.565-.142v.535q-.274.102-.565.149-.292.054-.697.054-.744 0-1.25-.31-.5-.309-.75-.875-.25-.571-.25-1.339 0-.745.268-1.31.274-.566.804-.881.529-.322 1.279-.322.78 0 1.352.286l-.244.524q-.226-.101-.506-.185-.274-.083-.607-.083m2.756 4.423h-.601v-5.215h.601z\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M86.498 20.771h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM86.361 15.31h-.619v-2.286h-2.513v2.286h-.613v-4.9h.613v2.072h2.513V10.41h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#1ff01f\" d=\"m6.875 19.188 5.843 3.372\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m81.404 20.142-5.023 2.899M81.404 20.142l-5.023 2.899M87.71 20.142l5.022 2.899M87.71 20.142l5.022 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003cg class=\"mol\"\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M118.385 23.072q-.786 0-1.238.53-.453.524-.453 1.447 0 .911.417 1.447.423.529 1.268.529.322 0 .607-.053.292-.06.566-.143v.536q-.274.101-.566.149-.291.053-.696.053-.744 0-1.25-.309-.5-.31-.75-.876-.25-.571-.25-1.339 0-.744.267-1.31.274-.565.804-.881.53-.321 1.28-.321.78 0 1.351.286l-.244.523q-.226-.101-.506-.184-.273-.084-.607-.084m2.757 4.424h-.601v-5.215h.601zM115.478 27.496h-.619V25.21h-2.512v2.286h-.614v-4.9h.614v2.072h2.512v-2.072h.619z\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"Clophedrone hydrochloride","UNII":"VKP2A6NM3Y"}],"Salts":["hydrochloride"],"Scheduling":[{"gov":"Germany","ref":[],"schedule":"Anlage II substance"},{"gov":"United Kingdom","ref":[],"schedule":"Class B substance"}],"StereoisomerData":[{"Aliases":null,"PubChemId":null,"SMILES":"CN[C@H](C)C(=O)C1=CC(Cl)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 98.793 49.848\"\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 0h99v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M97.755 25.941 87.71 20.142M81.404 20.142l-10.045 5.799\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M71.709 25.941h-.7M71.959 28.118h-1.2M72.209 30.295h-1.7M72.459 32.473h-2.2M72.709 34.65h-2.7M72.959 36.827h-3.2M73.209 39.004h-3.7M73.459 41.181h-4.2\"/\u003e\u003c/g\u003e\u003cpath d=\"m71.359 25.941-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M56.941 19.025V7.002M59.38 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M56.941 7.002v6.011M59.38 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.161 18.321-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m44.962 25.941-13.203-7.628M42.524 27.349l-10.765-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m31.759 18.313-13.198 7.62M18.561 25.933 6.875 19.188\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m18.561 25.933.005 15.248M21 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m18.566 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m31.769 48.81 13.198-7.62M31.769 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m44.962 25.941.005 15.249\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M86.498 20.771h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM86.361 15.31h-.619v-2.286h-2.513v2.286h-.613v-4.9h.613v2.072h2.513V10.41h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M60.42 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.757 0-1.263-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T58.175.56q.733 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M2.906 16.499q-.786 0-1.239.53-.452.524-.452 1.447 0 .91.417 1.446.422.53 1.268.53.321 0 .607-.054.291-.059.565-.142v.535q-.274.102-.565.149-.292.054-.697.054-.744 0-1.25-.31-.5-.309-.75-.875-.25-.571-.25-1.339 0-.745.268-1.31.274-.566.804-.881.529-.322 1.279-.322.78 0 1.352.286l-.244.524q-.226-.101-.506-.185-.274-.083-.607-.083m2.756 4.423h-.601v-5.215h.601z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m87.71 20.142 5.022 2.899M87.71 20.142l5.022 2.899M81.404 20.142l-5.023 2.899M81.404 20.142l-5.023 2.899\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m6.875 19.188 5.843 3.372\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(R)-Clophedrone","UNII":null},{"Aliases":null,"PubChemId":null,"SMILES":"CN[C@@H](C)C(=O)C1=CC(Cl)=CC=C1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 98.793 49.848\"\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 0h99v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M97.755 25.941 87.71 20.142M81.404 20.142l-10.045 5.799\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M71.709 25.941h-.7l-1.75 15.24h4.2z\" class=\"bond\"/\u003e\u003cpath d=\"m71.359 25.941-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M56.941 19.025V7.002M59.38 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M56.941 7.002v6.011M59.38 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.161 18.321-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m44.962 25.941-13.203-7.628M42.524 27.349l-10.765-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m31.759 18.313-13.198 7.62M18.561 25.933 6.875 19.188\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m18.561 25.933.005 15.248M21 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m18.566 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m31.769 48.81 13.198-7.62M31.769 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m44.962 25.941.005 15.249\" class=\"bond\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M86.498 20.771h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM86.361 15.31h-.619v-2.286h-2.513v2.286h-.613v-4.9h.613v2.072h2.513V10.41h.619z\"/\u003e\u003c/g\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M60.42 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.757 0-1.263-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T58.175.56q.733 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M2.906 16.499q-.786 0-1.239.53-.452.524-.452 1.447 0 .91.417 1.446.422.53 1.268.53.321 0 .607-.054.291-.059.565-.142v.535q-.274.102-.565.149-.292.054-.697.054-.744 0-1.25-.31-.5-.309-.75-.875-.25-.571-.25-1.339 0-.745.268-1.31.274-.566.804-.881.529-.322 1.279-.322.78 0 1.352.286l-.244.524q-.226-.101-.506-.185-.274-.083-.607-.083m2.756 4.423h-.601v-5.215h.601z\" class=\"atom\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m87.71 20.142 5.022 2.899M87.71 20.142l5.022 2.899M81.404 20.142l-5.023 2.899M81.404 20.142l-5.023 2.899\" class=\"hi\"/\u003e\u003cpath stroke=\"#1ff01f\" d=\"m6.875 19.188 5.843 3.372\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(S)-Clophedrone","UNII":null}],"StereoisomerType":"enantiomer","Stereoisomers":["(R)-Clophedrone","(S)-Clophedrone"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 98.793 49.848\"\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 0h99v50H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"M71.359 41.181v-15.24M71.359 25.941l-13.198-7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M56.941 19.025V7.002M59.38 19.025V7.002\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M56.941 7.002v6.011M59.38 7.002v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m58.161 18.321-13.199 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m44.962 25.941-13.203-7.628M42.524 27.349l-10.765-6.22\"/\u003e\u003c/g\u003e\u003cpath d=\"m31.759 18.313-13.198 7.62\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m18.561 25.933.005 15.248M21 27.34l.004 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m18.566 41.181 13.203 7.629\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m31.769 48.81 13.198-7.62M31.769 45.994l10.759-6.212\"/\u003e\u003c/g\u003e\u003cpath d=\"m44.962 25.941.005 15.249M18.561 25.933 6.875 19.188M71.359 25.941l10.045-5.799M87.71 20.142l10.045 5.799\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M60.42 3.078q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.757 0-1.263-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881T58.175.56q.733 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.221.53.839 0 1.22-.53.387-.536.387-1.459 0-.929-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524-.393.523-.393 1.452\" class=\"atom\"/\u003e\u003cpath fill=\"#1ff01f\" stroke=\"none\" d=\"M2.906 16.499q-.786 0-1.239.53-.452.524-.452 1.447 0 .91.417 1.446.422.53 1.268.53.321 0 .607-.054.291-.059.565-.142v.535q-.274.102-.565.149-.292.054-.697.054-.744 0-1.25-.31-.5-.309-.75-.875-.25-.571-.25-1.339 0-.745.268-1.31.274-.566.804-.881.529-.322 1.279-.322.78 0 1.352.286l-.244.524q-.226-.101-.506-.185-.274-.083-.607-.083m2.756 4.423h-.601v-5.215h.601z\" class=\"atom\"/\u003e\u003cg stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M86.498 20.771h-.721l-2.619-4.066h-.03l.03.595q.024.357.024.732v2.739h-.566v-4.9h.715l2.607 4.055h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.769h.578zM86.361 15.31h-.619v-2.286h-2.513v2.286h-.613v-4.9h.613v2.072h2.513V10.41h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#1ff01f\" d=\"m6.875 19.188 5.843 3.372\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m81.404 20.142-5.023 2.899M81.404 20.142l-5.023 2.899M87.71 20.142l5.022 2.899M87.71 20.142l5.022 2.899\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":{"Cognitive Effects":["Analysis enhancement","Ego inflation","Focus enhancement","Increased music appreciation","Motivation enhancement","Thought acceleration","Wakefulness","Disinhibition","Suggestibility suppression","Cognitive euphoria","Compulsive redosing","Mania"],"Physical Effects":["Increased libido","Stamina enhancement","Stimulation","Appetite suppression","Dehydration","Dry mouth","Restless legs","Shakiness","Teeth grinding","Abnormal heartbeat","Increased blood pressure","Increased heart rate","Vasoconstriction"],"Visual Effects":[]},"Title":"Clophedrone","UNII":"I2GB1C4TM7","Wikidata":"Q69911605","Wikipedia":"3-Chloromethcathinone","XLogP":2.2}