Pindobind

Pindobind
Nazivi
	IUPAC naziv 2-Bromo-N-[4-(2[2-hidroksi-3-(1H-indol-4-iloksi)propil]amino2-propanil)-1-metilcikloheksil]acetamid
Identifikacija
CAS broj	106469-52-7 ;
3D model (Jmol)	interaktivna slika;
ChemSpider	4661;
PubChem C ID	4827;
	SMILES BrCC(=O)NC1(C)CCC(CC1)C(NCC(O)COc2cccc3c2ccn3)(C)C; ; ; ; ; ;
Svojstva
Hemijska formula	C23H34BrN3O3
Molarna masa	480,45 g·mol−1
	Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
	Reference infokutije

Pindobind je hemikalija koji je patentirao IBM.^[3] On je eksperimentalno identifikovan kao depresant centralnog nervnog sistema.^[4] On kod životinja uzrokuje smanjenje ofanzivnih akcija, kao što je jurinje.^[4]

Reference

^ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
^ Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
^ PubChem 4827
^ ^а ^б 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. PMID 8255924. doi:10.1016/0091-3057(93)90318-N.

[1] Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

[2] Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.

[3] PubChem 4827

[Pmid-4] а ^б 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. PMID 8255924. doi:10.1016/0091-3057(93)90318-N.

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