Rescinamin

Rescinamin
(IUPAC) ime
	metil (3β,16β,17α,18β,20α)-11,17-dimetoksi-18[(2E)-3-(3,4,5-trimetoksifenil)prop-2-enoil]oksi}johimban-16-karboksilat
Klinički podaci
Identifikatori
CAS broj	24815-24-5
ATC kod	C02AA01
PubChem	5280954
DrugBank	DB01180
ChemSpider	4444446
UNII	Q6W1F7DJ2D
KEGG	D00198
ChEBI	CHEBI:28572
ChEMBL	CHEMBL1668
Hemijski podaci
Formula	C35H42N2O9
Mol. masa	634,716 g/mol
SMILES	eMolekuli & PubHem
InChI
	InChI=1S/C35H42N2O9/c1-40-21-8-9-22-23-11-12-37-18-20-15-29(46-30(38)10-7-19-13-27(41-2)33(43-4)28(14-19)42-3)34(44-5)31(35(39)45-6)24(20)17-26(37)32(23)36-25(22)16-21/h7-10,13-14,16,20,24,26,29,31,34,36H,11-12,15,17-18H2,1-6H3/b10-7+/t20-,24+,26-,29-,31+,34+/m1/s1 ; Key: SZLZWPPUNLXJEA-QEGASFHISA-N
Sinonimi	metil (1R,15S,17R,18R,19S,20S)-6,18-dimetoksi-17[(2E)-3-(3,4,5-trimetoksifenil)prop-2-enoil]oksi3,13-diazapentaciklo[11.8.0.02,10.04,9.015,20]henikosa-2(10),4(9),5,7-tetraen-19-karboksilat
Farmakoinformacioni podaci
Trudnoća	?
Pravni status	℞ Prescription only
Način primene	oralno

Rescinnamin je Inhibitor angiotenzin konvertujućeg enzima koji se koristi kao antihipertenziv.

On je vinka alkaloid koji se dobija iz biljke Rauwolfia serpentina^[6] i drugih Rauwolfia vrsta.^[7]

On je dostupan pod trgovačkim imenima: Moderil, Cinnasil, Anaprel.

ReferenceUredi

↑ 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
↑ 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.
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
↑ FIFE R, MACLAURIN JC, WRIGHT JH (December 1960). „Rescinnamine in treatment of hypertension in hospital clinic and in general practice”. British Medical Journal 2 (5216): 1848–50. DOI:10.1136/bmj.2.5216.1848. PMC 2098607. PMID 13699407.
↑ Balsevich J, Constabel F, Kurz WG. (1982). „Alkaloids of Vinca major cv. Variegata.”. Planta Med. 44 (2): 91-3. PMID 17402086.

Spoljašnje vezeUredi

	Portal Medicina
	Portal Hemija

Molimo Vas, obratite pažnju na važno upozorenje u vezi tema o zdravlju (medicini).

[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] 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.

[5] Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[pmid13699407-6] FIFE R, MACLAURIN JC, WRIGHT JH (December 1960). „Rescinnamine in treatment of hypertension in hospital clinic and in general practice”. British Medical Journal 2 (5216): 1848–50. DOI:10.1136/bmj.2.5216.1848. PMC 2098607. PMID 13699407.

[7] Balsevich J, Constabel F, Kurz WG. (1982). „Alkaloids of Vinca major cv. Variegata.”. Planta Med. 44 (2): 91-3. PMID 17402086.

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