Bietaserpine: Difference between revisions

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Bietaserpine
Identifiers
3D model (JSmol)	Interactive image;
ChemSpider	16735698;
ECHA InfoCard	Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value).
PubChem CID	65518;
	InChI InChI=1S/C39H53N3O9/c1-9-40(10-2)15-16-42-29-20-25(45-3)11-12-26(29)27-13-14-41-22-24-19-33(37(49-7)34(39(44)50-8)28(24)21-30(41)35(27)42)51-38(43)23-17-31(46-4)36(48-6)32(18-23)47-5/h11-12,17-18,20,24,28,30,33-34,37H,9-10,13-16,19,21-22H2,1-8H3/t24-,28+,30-,33-,34+,37+/m1/s1 Key: WFTSRDISOMSAQC-ZNFOTRSXSA-N; InChI=1/C39H53N3O9/c1-9-40(10-2)15-16-42-29-20-25(45-3)11-12-26(29)27-13-14-41-22-24-19-33(37(49-7)34(39(44)50-8)28(24)21-30(41)35(27)42)51-38(43)23-17-31(46-4)36(48-6)32(18-23)47-5/h11-12,17-18,20,24,28,30,33-34,37H,9-10,13-16,19,21-22H2,1-8H3/t24-,28+,30-,33-,34+,37+/m1/s1 Key: WFTSRDISOMSAQC-ZNFOTRSXBI;
	SMILES COc1cc(cc(OC)c1OC)C(=O)O[C@@H]4C[C@@H]5CN6CCc3c(n(CCN(CC)CC)c2cc(OC)ccc23)[C@H]6C[C@@H]5[C@H](C(=O)OC)[C@H]4OC;
Properties
Chemical formula	C39H53N3O9
Molar mass	707.87 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

VisualWikitext

Latest revision as of 18:08, 18 August 2015

Template:Chembox E number

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Bietaserpine (INN), or 1-diaminoethylreserpine, is a derivative of reserpine used as an antihypertensive agent. Like reserpine, bietaserpine is probably a VMAT inhibitor.^[1]

References

↑ Buckingham J et al. (eds.) (1993). Dictionary of Natural Products, vol. 5, p. 4923, Boca Raton: Chapman & Hall/CRC. ISBN 978-0-412-46620-5. Retrieved on June 22, 2009 through Google Book Search.

[1] Buckingham J et al. (eds.) (1993). Dictionary of Natural Products, vol. 5, p. 4923, Boca Raton: Chapman & Hall/CRC. ISBN 978-0-412-46620-5. Retrieved on June 22, 2009 through Google Book Search.

[1]

@@ Line 33: / Line 33: @@
    }}
 }}
+__NOTOC__
+{{SI}}
+{{CMG}}
+==Overview==
 '''Bietaserpine''' ([[International Nonproprietary Name|INN]]), or '''1-diaminoethylreserpine''', is a derivative of [[reserpine]] used as an [[antihypertensive drugs|antihypertensive agent]]. Like reserpine, bietaserpine is probably a [[VMAT]] inhibitor.<ref>Buckingham J ''et al.'' (eds.) (1993). ''[http://books.google.com.br/books?id=P4aNJh3pv2UC&pg=PA4923 Dictionary of Natural Products]'', vol. 5, p. 4923, Boca Raton: Chapman & Hall/CRC. ISBN 978-0-412-46620-5. Retrieved on June 22, 2009 through [[Google Book Search]].</ref>
 ==References==
-{{Reflist}}
+{{Reflist|2}}
 [[Category:Antihypertensive agents]]
 [[Category:Drug]]
 [[Category:Cardiovascular Drugs]]

Identifiers

3D model (JSmol)	Interactive image
ChemSpider	16735698
ECHA InfoCard	Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value).
PubChem CID	65518
InChI InChI=1S/C39H53N3O9/c1-9-40(10-2)15-16-42-29-20-25(45-3)11-12-26(29)27-13-14-41-22-24-19-33(37(49-7)34(39(44)50-8)28(24)21-30(41)35(27)42)51-38(43)23-17-31(46-4)36(48-6)32(18-23)47-5/h11-12,17-18,20,24,28,30,33-34,37H,9-10,13-16,19,21-22H2,1-8H3/t24-,28+,30-,33-,34+,37+/m1/s1 Key: WFTSRDISOMSAQC-ZNFOTRSXSA-N InChI=1/C39H53N3O9/c1-9-40(10-2)15-16-42-29-20-25(45-3)11-12-26(29)27-13-14-41-22-24-19-33(37(49-7)34(39(44)50-8)28(24)21-30(41)35(27)42)51-38(43)23-17-31(46-4)36(48-6)32(18-23)47-5/h11-12,17-18,20,24,28,30,33-34,37H,9-10,13-16,19,21-22H2,1-8H3/t24-,28+,30-,33-,34+,37+/m1/s1 Key: WFTSRDISOMSAQC-ZNFOTRSXBI
SMILES COc1cc(cc(OC)c1OC)C(=O)O[C@@H]4C[C@@H]5CN6CCc3c(n(CCN(CC)CC)c2cc(OC)ccc23)[C@H]6C[C@@H]5[C@H](C(=O)OC)[C@H]4OC
Properties
Chemical formula	C₃₉H₅₃N₃O₉
Molar mass	707.87 g·mol⁻¹
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is ^YN ?)
Infobox references

Bietaserpine: Difference between revisions

Latest revision as of 18:08, 18 August 2015

Overview

References

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