Kalusteron

Kalusteron
Nazivi
IUPAC naziv
(1S,2R,9S,10R,11S,14S,15S)-14-hidroksi-2,9,14,15-tetrametiltetraciklo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-on
Identifikacija
3D model (Jmol)
ChemSpider
DrugBank
  • [H][C@@]12CC[C@](C)(O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])[C@@H](C)CC2=CC(=O)CC[C@]12C
Svojstva
C21H32O2
Molarna masa 316,4776
Tačka topljenja 128
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
Зелена квачицаДа verifikuj (šta je Зелена квачицаДаRed КрстићНе ?)
Reference infokutije

Kalusteron je oralno aktivni androgeni steroid koji je alkilisan u poziciji 17. On je kontrolisana supstanca u Kanadi.[3][4][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. 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. ^ Meli, R. J.; Ros, P. R. (1992). „MR appearance of intra-abdominal metastatic melanoma”. Magnetic Resonance Imaging. 10 (4): 705—8. PMID 1501542. doi:10.1016/0730-725x(92)90024-t. 
  4. ^ Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS (2011). „DrugBank 3.0: a comprehensive resource for omics research on drugs”. Nucleic Acids Res.. 39 (Database issue): D1035—41. PMC 3013709 Слободан приступ. PMID 21059682. doi:10.1093/nar/gkq1126. 
  5. ^ Wishart DS, Knox C, Guo AC, Cheng D, Shrivastava S, Tzur D, Gautam B, Hassanali M (Nucleic Acids Res) (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. Nucleic Acids Research. 36 (Database issue): D901—6. PMC 2238889 Слободан приступ. PMID 18048412. doi:10.1093/nar/gkm958. 

Spoljašnje veze

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