U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry EPIMERIC
Molecular Formula C19H19N.C4H6O6
Molecular Weight 411.4477
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENINDAMINE TARTRATE

SMILES

O[C@H]([C@@H](O)C(O)=O)C(O)=O.CN1CCC2=C(C1)C(C3=CC=CC=C23)C4=CC=CC=C4

InChI

InChIKey=WFXURHIXPXVPGM-LREBCSMRSA-N
InChI=1S/C19H19N.C4H6O6/c1-20-12-11-16-15-9-5-6-10-17(15)19(18(16)13-20)14-7-3-2-4-8-14;5-1(3(7)8)2(6)4(9)10/h2-10,19H,11-13H2,1H3;1-2,5-6H,(H,7,8)(H,9,10)/t;1-,2-/m.1/s1

HIDE SMILES / InChI

Molecular Formula C4H6O6
Molecular Weight 150.0868
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula C19H19N
Molecular Weight 261.3609
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/18907211

Phenindamine (thephorin or 2-methyl-9-phenyl-2,3,4,9-tetrahydro-1-pyridindene) a pyridindene derivative proved to be a potent antihistaminic. Phenindamine was used to treat sneezing; runny nose; itching, watery eyes; hives; rashes; itching; and other symptoms of allergies and the common cold.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
THEPHORIN

Approved Use

Phenindamine was used to treat sneezing; runny nose; itching, watery eyes; hives; rashes; itching; and other symptoms of allergies and the common cold.

Launch Date

-7.1634243E11
PubMed

PubMed

TitleDatePubMed
Treatment of allergic and some other dermatoses with thephorin; a preliminary report.
1947 Aug
Thephorin in the treatment of disseminated neurodermatitis.
1948 Aug
Histamine and the antihistaminic drugs.
1950 May
Performance enhancement effects of d-amphetamine, methylphenidate, pipradrol and phenindamine in rats.
1976
The histamine H1-receptor antagonist binding site. A stereoselective pharmacophoric model based upon (semi-)rigid H1-antagonists and including a known interaction site on the receptor.
1995 Aug 18
Patents

Patents

Sample Use Guides

The maximum amount of phenindamine that you should take in 1 day is 75 mg.
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:01:16 UTC 2023
Edited
by admin
on Fri Dec 15 15:01:16 UTC 2023
Record UNII
28725X3PV8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENINDAMINE TARTRATE
MART.   USAN   VANDF   WHO-DD  
USAN  
Official Name English
PHENINDAMINE BITARTRATE
Common Name English
PERNOVINE
Common Name English
NOLAHIST
Brand Name English
1H-INDENO(2,1-C)PYRIDINE, 2,3,4,9-TETRAHYDRO-2-METHYL-9-PHENYL-, (R-(R*,R*))-2,3-DIHYDROXYBUTANEDIOATE (1:1)
Common Name English
PHENINDAMINE TARTRATE [VANDF]
Common Name English
PERNOVIN
Brand Name English
THEPHORIN TARTRATE
Common Name English
2,3,4,9-TETRAHYDRO-2-METHYL-9-PHENYL-1H-INDENO(2,1-C)PYRIDINE TARTRATE
Systematic Name English
PHENINDAMINE TARTRATE [USAN]
Common Name English
2,3,4,9-TETRAHYDRO-2-METHYL-9-PHENYL-1H-INDENO-(2,1-C)PYRIDINE BITARTRATE
Systematic Name English
NSC-91526
Code English
1H-INDENO(2,1-C)PYRIDINE, 2,3,4,9-TETRAHYDRO-2-METHYL-9-PHENYL-, (2R,3R)-2,3-DIHYDROXYBUTANEDIOATE (1:1)
Systematic Name English
PHENINDAMINE TARTRATE [MART.]
Common Name English
PHENINDAMINE HYDROGEN TARTRATE [MI]
Common Name English
Phenindamine tartrate [WHO-DD]
Common Name English
1H-INDENO(2,1-C)PYRIDINE, 2,3,4,9-TETRAHYDRO-2-METHYL-9-PHENYL-, TARTRATE (1:1)
Systematic Name English
PHENINDAMINE HYDROGEN TARTRATE
MI  
Common Name English
Classification Tree Code System Code
CFR 21 CFR 341.12
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
NCI_THESAURUS C29578
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
Code System Code Type Description
CAS
569-59-5
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
CAS
31348-79-5
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
SUPERSEDED
EPA CompTox
DTXSID40972338
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
DRUG BANK
DBSALT002846
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
ChEMBL
CHEMBL278398
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
MERCK INDEX
m8617
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY Merck Index
EVMPD
SUB03745MIG
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
ECHA (EC/EINECS)
209-320-7
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
PUBCHEM
11290
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
NCI_THESAURUS
C87746
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
FDA UNII
28725X3PV8
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
RXCUI
221137
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY RxNorm
NSC
91526
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
SMS_ID
100000085682
Created by admin on Fri Dec 15 15:01:16 UTC 2023 , Edited by admin on Fri Dec 15 15:01:16 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY