| Pindobind |
 |
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 |
| PubChem |
4827 |
| ChemSpider |
4661 |
| Jmol-3D images |
Image 1 |
-
BrCC(=O)NC1(C)CCC(CC1)C(NCC(O)COc2cccc3c2ccn3)(C)C
|
-
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
|
| Properties |
| Molecular formula |
C23H34BrN3O3 |
| Molar mass |
480.44 g mol−1 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
| Infobox references |
Pindobind is a chemical patented by IBM.[1]It has experimentally been identified as a central nervous system depressant[2] which generated a response in animals of reducing offensive actions such as chasing, while also notably reducing tendencies of the test animal to evade when stimulated to do so.[2]
References [edit]
- ^ PubChem 4827
- ^ a b Bell, R; Hobson, H (1993). "Effects of pindobind 5-hydroxytryptamine1A (5-HT1A), a novel and potent 5-HT1A antagonist, on social and agonistic behaviour in male albino mice". Pharmacology, Biochemistry, and Behavior 46 (1): 67–72. doi:10.1016/0091-3057(93)90318-N. PMID 8255924.
