Pindobind

Pindobind
	2-Bromo-N-[4-(2[2-hidroksi-3-(1H-indol-4-iloksi)propil]amino2-propanil)-1-metilcikloheksil]acetamid
Identifikacija
CAS registarski broj	106469-52-7
PubChem	4827
ChemSpider	4661
Jmol-3D slike	Slika 1
SMILES
	BrCC(=O)NC1(C)CCC(CC1)C(NCC(O)COc2cccc3c2ccn3)(C)C
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) ; Kod: 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); Kod: XSAGAZCYTLNCEN-UHFFFAOYAL
Svojstva
Molekulska formula	C23H34BrN3O3
Molarna masa	480.44 g mol−1
	; ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Pindobind je hemikalija koji je patentirao IBM.^[4] On je eksperimentalno identifikovan kao depresant centralnog nervnog sistema.^[5] On kod životinja uzrokuje smanjenje ofanzivnih akcija, kao što je jurinje.^[5]

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. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ 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.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ PubChem 4827
↑ ^5,0 ^5,1 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.

[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. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[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] Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[4] PubChem 4827

[Pmid-5] 5,0 ^5,1 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.

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