ALPHAPRODINE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C16H23NO2
Molecular Weight	261.3593
Optical Activity	( + / - )
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of ALPHAPRODINE

Structure Search

SMILES

CCC(=O)O[C@@]1(CCN(C)C[C@@H]1C)C2=CC=CC=C2

InChI

InChIKey=UVAZQQHAVMNMHE-XJKSGUPXSA-N

InChI=1S/C16H23NO2/c1-4-15(18)19-16(14-8-6-5-7-9-14)10-11-17(3)12-13(16)2/h5-9,13H,4,10-12H2,1-3H3/t13-,16+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C16H23NO2
Molecular Weight	261.3593
Charge	0
Count

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

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:04:49 UTC 2023` Edited by `admin` on `Fri Dec 15 15:04:49 UTC 2023`
Record UNII	001O2254AC
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ALPHAPRODINE

Official Name

English

ACSCN-9010

Common Name

English

alphaprodine [INN]

Common Name

English

DL-.ALPHA.-PRODINE

Common Name

English

ALPHAPRODINE [HSDB]

Common Name

English

NISINTIL

Common Name

English

.ALPHA.-1,3-DIMETHYL-4-PHENYL-4-PROPIONOXYPIPERIDINE

Common Name

English

(±)-1,3-DIMETHYL-4-PHENYL-4-PIPERIDINOL PROPIONATE (ESTER)

Common Name

English

PRISILIDIN

Common Name

English

ALPHAPRODINE [MI]

Common Name

English

ALPHAPRODINE [VANDF]

Common Name

English

IDS-NA-011

Code

English

Alphaprodine [WHO-DD]

Common Name

English

4-PIPERIDINOL, 1,3-DIMETHYL-4-PHENYL-, PROPANOATE (ESTER), CIS-(±)-

Common Name

English

Classification Tree Code System Code

DEA NO.

9010

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

NCI_THESAURUS

C67413

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

Code System Code Type Description

NCI_THESAURUS

C83528

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

PRIMARY

ChEMBL

CHEMBL1623765

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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SMS_ID

100000087470

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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WIKIPEDIA

Prodine

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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FDA UNII

001O2254AC

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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CAS

77-20-3

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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DRUG BANK

DB13160

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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INN

1063

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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HSDB

3283

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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DRUG CENTRAL

132

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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RXCUI

594

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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RxNorm

EVMPD

SUB05366MIG

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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PUBCHEM

120738

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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MERCK INDEX

m1576

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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Merck Index

MESH

D000522

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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ECHA (EC/EINECS)

201-011-5

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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EPA CompTox

DTXSID4022575

Created by admin on Fri Dec 15 15:04:49 UTC 2023 , Edited by admin on Fri Dec 15 15:04:49 UTC 2023

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Related Record Type Details


					CO51Q2EI5Z

ALPHAPRODINE HYDROCHLORIDE

SALT/SOLVATE -> PARENT

Comments:

APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)

Amount:

Related Record Type Details


					001O2254AC

ACTIVE MOIETY