GEISSOSCHIZOLINE METHIODIDE

Details

Stereochemistry	UNKNOWN
Molecular Formula	C20H29N2O.I
Molecular Weight	440.3615
Optical Activity	UNSPECIFIED
Defined Stereocenters	6 / 7
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of GEISSOSCHIZOLINE METHIODIDE

Structure Search

SMILES

[I-].CC[C@@H]1C[N+]2(C)CC[C@@]34[C@@H](NC5=C3C=CC=C5)[C@@H](CO)[C@H]1C[C@H]24

InChI

InChIKey=BPUDSGVMWJBRMI-DNDBAWMXSA-M

InChI=1S/C20H29N2O.HI/c1-3-13-11-22(2)9-8-20-16-6-4-5-7-17(16)21-19(20)15(12-23)14(13)10-18(20)22;/h4-7,13-15,18-19,21,23H,3,8-12H2,1-2H3;1H/q+1;/p-1/t13-,14+,15+,18+,19+,20-,22?;/m1./s1

HIDE SMILES / InChI

Molecular Formula	HI
Molecular Weight	127.91241
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	C20H28N2O
Molecular Weight	312.4491
Charge	0
Count

Stereochemistry	EPIMERIC
Additional Stereochemistry	No
Defined Stereocenters	6 / 7
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 23:26:18 GMT 2025` Edited by `admin` on `Mon Mar 31 23:26:18 GMT 2025`
Record UNII	402QU7LR2B
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

GEISSOSCHIZOLINE METHIODIDE [MI]

Preferred Name

English

GEISSOSCHIZOLINE METHIODIDE

Common Name

English

CURANIUM, 17-HYDROXY-4-METHYL-, IODIDE, (16.ALPHA.)-

Systematic Name

English

N-METHYLPEREIRINIUM IODIDE

Common Name

English

PEREIRINE METHIODIDE

Common Name

English

Code System Code Type Description

CAS

103458-77-1

Created by admin on Mon Mar 31 23:26:18 GMT 2025 , Edited by admin on Mon Mar 31 23:26:18 GMT 2025

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FDA UNII

402QU7LR2B

Created by admin on Mon Mar 31 23:26:18 GMT 2025 , Edited by admin on Mon Mar 31 23:26:18 GMT 2025

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MERCK INDEX

m5683

Created by admin on Mon Mar 31 23:26:18 GMT 2025 , Edited by admin on Mon Mar 31 23:26:18 GMT 2025

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Merck Index

PUBCHEM

90479501

Created by admin on Mon Mar 31 23:26:18 GMT 2025 , Edited by admin on Mon Mar 31 23:26:18 GMT 2025

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