PHYSOVENINE

CNC(=O)OC1=CC2=C(C=C1)N(C)[C@H]3OCC[C@@]23C

InChIKey=LXTKNVLLWOLCOV-JSGCOSHPSA-N

InChI=1S/C14H18N2O3/c1-14-6-7-18-12(14)16(3)11-5-4-9(8-10(11)14)19-13(17)15-2/h4-5,8,12H,6-7H2,1-3H3,(H,15,17)/t12-,14-/m0/s1

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

PubMed

Title	Date	PubMed
An interrupted Fischer indolization approach toward fused indoline-containing natural products.	2009-08-06	19601608
Accommodation of physostigmine and its analogues by acetylcholinesterase is dominated by hydrophobic interactions.	2009-01-01	18729824
Novel anticholinesterases based on the molecular skeletons of furobenzofuran and methanobenzodioxepine.	2005-02-24	15715468
Efficient formal total synthesis of physostigmine and physovenine: conformational analysis of key intermediates.	2002-02	11858744

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:50:38 GMT 2025` Edited by `admin` on `Mon Mar 31 21:50:38 GMT 2025`
Record UNII	H67Q5553UW
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

(-)-PHYSOVENINE

Preferred Name

English

PHYSOVENINE

Common Name

English

2H-FURO(2,3-B)INDOL-5-OL, 3,3A,8,8A-TETRAHYDRO-3A,8-DIMETHYL-, METHYLCARBAMATE (ESTER), (3AS-CIS)-

Systematic Name

English

2H-FURO(2,3-B)INDOL-5-OL, 3,3A,8,8A-TETRAHYDRO-3A,8-DIMETHYL-, 2-(N-METHYLCARBAMATE), (3AS,8AS)-

Systematic Name

English

PHYSOVENINE [MI]

Common Name

English

Code System Code Type Description

PUBCHEM

442113