Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C19H22BrNO3 |
| Molecular Weight | 392.287 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C2[C@H](CNCC3=C(OC)C=CC=C3)CC2=C(OC)C(Br)=C1
InChI
InChIKey=CLSBQRBXTFTLEX-ZDUSSCGKSA-N
InChI=1S/C19H22BrNO3/c1-22-16-7-5-4-6-12(16)10-21-11-13-8-14-18(13)17(23-2)9-15(20)19(14)24-3/h4-7,9,13,21H,8,10-11H2,1-3H3/t13-/m0/s1
Approval Year
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
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WIKIPEDIA |
Designer-drugs-2CBCB-NBOMe
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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| Code System | Code | Type | Description | ||
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1354634-09-5
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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PRIMARY | |||
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WGI3S41A26
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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PRIMARY | |||
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2CBCB-NBOME
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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PRIMARY | 2CBCB-NBOMe (NBOMe-TCB-2) is a compound indirectly derived from the phenethylamine series of hallucinogens, which was discovered in 2007 at Purdue University as part of the ongoing research program of the team led by David Nichols focusing on the mapping of the specific amino acid residues responsible for ligand binding to the 5HT2A receptor. 2CBCB-NBOMe acts as a potent and selective agonist for the 5-HT2A and 5-HT2C receptors, with a Ki of 0.27nM at the human 5-HT2A receptor, a similar potency to other agonists such as TCB-2, NBOMe-2C-I and Bromo-DragonFLY. | ||
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DTXSID501028189
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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PRIMARY | |||
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57483909
Created by
admin on Mon Mar 31 23:08:26 GMT 2025 , Edited by admin on Mon Mar 31 23:08:26 GMT 2025
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PRIMARY |
ACTIVE MOIETY
