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Details

Stereochemistry RACEMIC
Molecular Formula C19H19N.ClH
Molecular Weight 297.822
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENINDAMINE HYDROCHLORIDE

SMILES

Cl.CN1CCC2=C(C1)C(C3=CC=CC=C23)C4=CC=CC=C4

InChI

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

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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 effects of phenindamine tartrate on sleepiness and psychomotor performance.
1992 Dec
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 Sat Dec 16 08:39:02 UTC 2023
Edited
by admin
on Sat Dec 16 08:39:02 UTC 2023
Record UNII
2B049A11FH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENINDAMINE HYDROCHLORIDE
MI  
Common Name English
1H-INDENO(2,1-C)PYRIDINE, 2,3,4,9-TETRAHYDRO-2-METHYL-9-PHENYL-, HYDROCHLORIDE (1:1)
Systematic Name English
PHENINDAMINE HYDROCHLORIDE [MI]
Common Name English
1H-INDENO(2,1-C)PYRIDINE, 2,3,4,9-TETRAHYDRO-2-METHYL-9-PHENYL-, HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID90970389
Created by admin on Sat Dec 16 08:39:02 UTC 2023 , Edited by admin on Sat Dec 16 08:39:02 UTC 2023
PRIMARY
PUBCHEM
21673
Created by admin on Sat Dec 16 08:39:02 UTC 2023 , Edited by admin on Sat Dec 16 08:39:02 UTC 2023
PRIMARY
FDA UNII
2B049A11FH
Created by admin on Sat Dec 16 08:39:02 UTC 2023 , Edited by admin on Sat Dec 16 08:39:02 UTC 2023
PRIMARY
MERCK INDEX
m8617
Created by admin on Sat Dec 16 08:39:02 UTC 2023 , Edited by admin on Sat Dec 16 08:39:02 UTC 2023
PRIMARY Merck Index
CAS
5503-08-2
Created by admin on Sat Dec 16 08:39:02 UTC 2023 , Edited by admin on Sat Dec 16 08:39:02 UTC 2023
PRIMARY
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