Pindobind

Pindobind is a compound developed by researchers associated with Stanford University,^[1] identified as a central nervous system depressant,^[2] which generated a response in animals reducing offensive actions such as chasing, while also notably reducing tendencies of the test animal to evade when stimulated to do so.^[2] It acts as an irreversible beta blocker and irreversible 5-HT_1A receptor antagonist.

Quick facts Names, Identifiers ...

Pindobind

Names
IUPAC name 2-Bromo-N-[4-(2-{[2-hydroxy-3-(1H-indol-4-yloxy)propyl]amino}-2-propanyl)-1-methylcyclohexyl]acetamide
Identifiers
CAS Number	106469-52-7 Y
3D model (JSmol)	Interactive image
ChemSpider	4661
PubChem CID	4827
CompTox Dashboard (EPA)	DTXSID80910012
InChI InChI=1S/C23H34BrN3O3/c1-22(2,16-7-10-23(3,11-8-16)27-21(29)13-24)26-14-17(28)15-30-20-6-4-5-19-18(20)9-12-25-19/h4-6,9,12,16-17,25-26,28H,7-8,10-11,13-15H2,1-3H3,(H,27,29) Key: XSAGAZCYTLNCEN-UHFFFAOYSA-N InChI=1/C23H34BrN3O3/c1-22(2,16-7-10-23(3,11-8-16)27-21(29)13-24)26-14-17(28)15-30-20-6-4-5-19-18(20)9-12-25-19/h4-6,9,12,16-17,25-26,28H,7-8,10-11,13-15H2,1-3H3,(H,27,29) Key: XSAGAZCYTLNCEN-UHFFFAOYAL
SMILES BrCC(=O)NC1(C)CCC(CC1)C(NCC(O)COc2cccc3c2cc[nH]3)(C)C
Properties
Chemical formula	C23H34BrN3O3
Molar mass	480.447 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Close