Deserpidine information

Deserpidine
Names
	IUPAC name Methyl 17α-methoxy-18β-[(3,4,5-trimethoxybenzoyl)oxy]-3β,20α-yohimban-16β-carboxylate
	Systematic IUPAC name Methyl (1S,2R,4R,4aS,13bR,14aS)-2-methoxy-3-[(3,4,5-trimethoxybenzoyl)oxy]-1,2,3,4,4a,5,7,8,13,13b,14,14a-dodecahydroindolo[2′,3′:3,4]pyrido[1,2-b]isoquinoline-1-carboxylate
Identifiers
CAS Number	131-01-1 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:27478 ;
ChEMBL	ChEMBL1200515 ;
ChemSpider	8232 ;
DrugBank	DB01089 ;
ECHA InfoCard	100.004.551
IUPHAR/BPS	7064;
KEGG	D08194 ;
PubChem CID	8550;
UNII	9016E3VB47 ;
CompTox Dashboard (EPA)	DTXSID8020383 ;
	InChI InChI=1S/C32H38N2O8/c1-37-24-12-17(13-25(38-2)29(24)39-3)31(35)42-26-14-18-16-34-11-10-20-19-8-6-7-9-22(19)33-28(20)23(34)15-21(18)27(30(26)40-4)32(36)41-5/h6-9,12-13,18,21,23,26-27,30,33H,10-11,14-16H2,1-5H3/t18-,21+,23-,26-,27+,30+/m1/s1 Key: CVBMAZKKCSYWQR-WCGOZPBSSA-N ; InChI=1/C32H38N2O8/c1-37-24-12-17(13-25(38-2)29(24)39-3)31(35)42-26-14-18-16-34-11-10-20-19-8-6-7-9-22(19)33-28(20)23(34)15-21(18)27(30(26)40-4)32(36)41-5/h6-9,12-13,18,21,23,26-27,30,33H,10-11,14-16H2,1-5H3/t18-,21+,23-,26-,27+,30+/m1/s1 Key: CVBMAZKKCSYWQR-WCGOZPBSBL;
	SMILES O=C(OC)[C@H]6[C@H]4C[C@@H]3c2[nH]c1ccccc1c2CCN3C[C@H]4C[C@@H](OC(=O)c5cc(OC)c(OC)c(OC)c5)[C@@H]6OC;
Properties
Chemical formula	C32H38N2O8
Molar mass	578.662 g·mol−1
Pharmacology
ATC code	C02AA05 (WHO)
	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

Deserpidine (INN) or reserpidine (USAN) is an antihypertensive drug structurally related to reserpine^[1] which occurs naturally in Rauvolfia spp.

^ Fulton, S. C.; Healy, M. D. (1976). "Comparison of the effectiveness of deserpidine, reserpine, and alpha-methyltyrosine on brain biogenic amines". Federation Proceedings. 35 (14): 2558–2562. PMID 11134.

[1] Fulton, S. C.; Healy, M. D. (1976). "Comparison of the effectiveness of deserpidine, reserpine, and alpha-methyltyrosine on brain biogenic amines". Federation Proceedings. 35 (14): 2558–2562. PMID 11134.

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