Pindobind

Pindobind
IUPAC ime
 
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 DaY
PubChem[1][2] 4827
ChemSpider[3] 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) DaY
Kod: XSAGAZCYTLNCEN-UHFFFAOYSA-N DaY

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

  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
  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.