NICOMORPHINE

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NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C29H25N3O5
Molecular Weight	495.5259
Optical Activity	UNSPECIFIED
Defined Stereocenters	5 / 5
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of NICOMORPHINE

Structure Search

SMILES

[H][C@@]12OC3=C(OC(=O)C4=CN=CC=C4)C=CC5=C3[C@@]16CCN(C)[C@]([H])(C5)[C@]6([H])C=C[C@@H]2OC(=O)C7=CN=CC=C7

InChI

InChIKey=HNDXBGYRMHRUFN-CIVUWBIHSA-N

InChI=1S/C29H25N3O5/c1-32-13-10-29-20-7-9-23(36-28(34)19-5-3-12-31-16-19)26(29)37-25-22(8-6-17(24(25)29)14-21(20)32)35-27(33)18-4-2-11-30-15-18/h2-9,11-12,15-16,20-21,23,26H,10,13-14H2,1H3/t20-,21+,23-,26-,29-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C29H25N3O5
Molecular Weight	495.5259
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	5 / 5
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 16:29:27 UTC 2023` Edited by `admin` on `Fri Dec 15 16:29:27 UTC 2023`
Record UNII	Y95FRL95FW
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NICOMORPHINE

Official Name

English

NICOMORPHINE [MI]

Common Name

English

MORPHINAN-3,6-DIOL, 7,8-DIDEHYDRO-4,5-EPOXY-17-METHYL- (5.ALPHA.,6.ALPHA.)-, 3,6-DI-3-PYRIDINECARBOXYLATE

Systematic Name

English

DEA NO. 9312

Common Name

English

MORPHINE ESTER WITH NICOTINIC ACID

Common Name

English

IDS-NN-003

Code

English

MORPHINE DINICOTINATE ESTER

Common Name

English

Nicomorphine [WHO-DD]

Common Name

English

MORPHINE DINICOTINATE

Common Name

English

3,6-DINICOTINOYLMORPHINE

Common Name

English

nicomorphine [INN]

Common Name

English

MORPHINE DINICOTINATE (ESTER)

Common Name

English

Classification Tree Code System Code

WHO-ATC

N02AA04

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

DEA NO.

9312

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

WHO-VATC

QN02AA04

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

Code System Code Type Description

DRUG BANK

DB13454

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

PRIMARY

FDA UNII

Y95FRL95FW

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

PRIMARY

MESH

C008549

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

PRIMARY

ECHA (EC/EINECS)

211-357-9

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

PRIMARY

CAS

639-48-5

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

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SMS_ID

100000084397

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

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MERCK INDEX

m7875

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

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Merck Index

EVMPD

SUB09241MIG

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

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NCI_THESAURUS

C170218

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

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DRUG CENTRAL

1918

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

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INN

789

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

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PUBCHEM

5362460

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

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WIKIPEDIA

NICOMORPHINE

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

PRIMARY

ChEMBL

CHEMBL2106851

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

PRIMARY

EPA CompTox

DTXSID00213517

Created by admin on Fri Dec 15 16:29:27 UTC 2023 , Edited by admin on Fri Dec 15 16:29:27 UTC 2023

PRIMARY

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NICOMORPHINE HYDROCHLORIDE

SALT/SOLVATE -> PARENT

Comments:

APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)

Amount:

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