Enprostil

Enprostil
(IUPAC) ime
Metil 7-[(1S,2S,3S)- 3-hidroksi-2-[(S,E)-3-hidroksi-4-fenoksibut-1-enil]-5-oksociklopentil]hepta-4,5-dienoat
Klinički podaci
AHFS/Drugs.com Internacionalno ime leka
Identifikatori
CAS broj 73121-56-9
ATC kod A02BB02
PubChem[1][2] 51744
UNII J4IP5Z9DAU DaY
KEGG[3] D01891 DaY
Hemijski podaci
Formula C23H28O6 
Mol. masa 400,46 g/mol
SMILES eMolekuli & PubHem
InChI
InChI=1S/C23H28O6/c1-28-23(27)12-8-3-2-7-11-19-20(22(26)15-21(19)25)14-13-17(24)16-29-18-9-5-4-6-10-18/h3-7,9-10,13-14,17,19-20,22,24,26H,8,11-12,15-16H2,1H3/t2?,17-,19+,20+,22+/m1/s1 DaY
Key: PTOJVMZPWPAXER-JRIPZDIHSA-N DaY
Farmakoinformacioni podaci
Trudnoća ?
Pravni status

Enprostil je sintetički prostaglandin koji je sličan sa dinoprostonom. Enprostil je veoma potentan inhibitor sekrecije želudačne HCl.[4]

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. ↑ Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H. 
  4. ↑ Roszkowski, AP; Garay, GL; Baker, S; Schuler, M; Carter, H (1986). „Gastric antisecretory and antiulcer properties of enprostil, (+/-)-11 alpha, 15 alpha-dihydroxy-16-phenoxy-17,18,19,20-tetranor-9-oxoprosta- 4,5,13(t)-trienoic acid methyl ester”. The Journal of Pharmacology and Experimental Therapeutics 239 (2): 382–9. PMID 3095537. 

Literatura

  • Toshina, K.; Hirata, I.; Maemura, K.; Sasaki, S.; Murano, M.; Nitta, M.; Yamauchi, H.; Nishikawa, T. i dr.. (2000). „Enprostil, a Prostaglandin-E2 Analogue, Inhibits Interleukin-8 Production of Human Colonic Epithelial Cell Lines”. Scandinavian Journal of Immunology 52 (6): 570–5. DOI:10.1046/j.1365-3083.2000.00815.x. PMID 11119262. 
  • Tari, Akira; Hamada, Masanori; Kamiyasu, Toshiki; Sumii, Koji; Haruma, Ken; Inoue, Masaki; Kishimoto, Shinya; Kajiyama, Goro i dr.. (1997). „Effect of enprostil on omeprazole-induced hypergastrinemia and inhibition of gastric acid secretion in peptic ulcer patients”. Digestive Diseases and Sciences 42 (8): 1741–6. DOI:10.1023/A:1018825902055. PMID 9286243. 
  • Ching, C. K.; Lam, S. K. (1995). „A comparison of two prostaglandin analogues (enprostil vs misoprostol) in the treatment of acute duodenal ulcer disease”. Journal of Gastroenterology 30 (5): 607–14. DOI:10.1007/BF02367786. PMID 8574332. 

Spoljašnje veze

Portal Medicina
Portal Hemija
  • p
  • r
  • u
PrekursorProstanoidi
Prekursor
H2
Aktivni
D/J
D2
E/F
E2 (Dinoproston): Enprostil • Sulproston

E1 (Alprostadil): Mizoprostol • Gemeprost

F2α (Dinoprost): Bimatoprost • Karboprost • Latanoprost • Tafluprost • Travoprost • Unoproston
I
I2 (Prostaciklin/Epoprostenol): Beraprost • Iloprost • Treprostinil
A2 • B2
Leukotrieni (LT)
Prekursor
Inicijalni
A4 • B4
C4 • D4 • E4
Neklasični
Lipoksini (A4, B4) • Virodhamin
Po funkciji
bronhokonstrikcija (PGF2α, TXA2, LTC4, LTD4, LTE4)

vazokonstrikcija (PGF2α, TXA2, TXB2) • vazodilatacija (PGE2, PGI2, LTC4, LTD4, LTE4)

trombociti: indukuje (TXA2) inhibira (PGD2, PGI2) • leukociti: indukuje (TXA2, LTB4) inhibira (PGD2, PGE2)

Porođaj stimulacija: (PGE2 (Dinoproston), PGF2α (Dinoprost))

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)

Biohemijske familije: Ugljeni hidrati (Glikozidi,Alkoholi) • Lipidi (Steroidi,Fosfolipidi,Glikolipidi,Masne kiseline,Tetrapiroli) • Proteini (Aminokiseline,Peptidi,Glikoproteini) • Nukleobaze/Nukleinske kiseline