Demoksitocin

{{chembox-lat |ImageFile=Demoxytocin.svg |ImageSize= |IUPACName= 2-[(1-{[13-(butan-2-yl)-10-(2-carbamoylethyl)-7-(carbamoylmethyl)-16-[(4-hydroxyphenyl)methyl]-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentaazacycloicosan-4-yl]carbonyl}pyrrolidin-2-yl)formamido]-N-(carbamoylmethyl)-4-methylpentanamide |OtherNames= |Section1=! colspan=2 style="background: #f8eaba; text-align: center;" |Identifikacija

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CAS broj

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3D model (Jmol)

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| ECHA InfoCard | 100.003.668 |-



| MeSH | deaminooxytocin |-

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PubChem[1][2] C ID

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  • CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(CSSCCC(=O)NC(C(=O)N1)CC2=CC=C(C=C2)O)C(=O)N3CCCC3C(=O)NC(CC(C)C)C(=O)NCC(=O)N)CC(=O)N)CCC(=O)N

|- |Section2=! colspan=2 style="background: #f8eaba; text-align: center;" |Svojstva

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Hemijska formula

| C43H65N11O12S2

|- | Molarna masa

| 992,1727

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Demoksitocin (INN, trgovačko ime Sandopart) ili deaminooksitocin, je akušerski lek koji se koristi za prevenciju postnatalnog mastitisa.[3][4] On je analogan oksitocinu.

  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. ^ Ulstein M, Sagen N, Eikhom SN (1979). „A comparative study of labor induced by oral prostaglandin E2 and buccal tablets of demoxytocin”. Int J Gynaecol Obstet. 17 (3): 243—5. PMID 42577. 
  4. ^ Lykkesfeldt G, Osler M (1981). „Induction of labor with oral prostaglandin E2 and buccal demoxytocin without amniotomy”. Acta Obstet Gynecol Scand. 60 (4): 429—30. PMID 7282312. 

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