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Details

Stereochemistry ACHIRAL
Molecular Formula C10H14ClN.ClH
Molecular Weight 220.139
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORPHENTERMINE HYDROCHLORIDE

SMILES

Cl.CC(C)(N)CC1=CC=C(Cl)C=C1

InChI

InChIKey=WEJDYJKJPUPMLH-UHFFFAOYSA-N
InChI=1S/C10H14ClN.ClH/c1-10(2,12)7-8-3-5-9(11)6-4-8;/h3-6H,7,12H2,1-2H3;1H

HIDE SMILES / InChI

Molecular Formula C10H14ClN
Molecular Weight 183.678
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/13931448 | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2274216/pdf/canfamphys00340-0041.pdf

Chlorphentermine exerts anorectic properties. It is a synthetic amphetamine derivatc claimed to have none of the excitatory effects of the parenit substanice. PRE-SATE (Chlorphentermine HCl) is an effective appetite suppressant with a pattern of pharmacologic action substantially different from those of traditional anorexigenics. In providing dependable appetite control with appreciable loss of bodyweight, PRE-SATE does not significantly increase central nervous system (CNS), cardiorespiratory or metabolic activity.

CNS Activity

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
338.0 nM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
PRE-SATE

Approved Use

PRE-SATE is indicated as an adlunct in the short term (i.e. a few weeks) management of exogenous obesity and related less serious overweight conditions in conjunction with a medically supervised regimen of weight reduction based on caloric restriction.
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
0.4 μg/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CHLORPHENTERMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
10.6 μg × h/mL
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CHLORPHENTERMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
41 h
100 mg single, oral
dose: 100 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
CHLORPHENTERMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
PubMed

PubMed

TitleDatePubMed
Chlorphentermine, a new anorectic agent.
1962 Sep
Experimental myopathy induced by amphiphilic cationic compounds including several psychotropic drugs.
1979
The early changes in experimental myopathy induced by chloroquine and chlorphentermine.
1980 Jan
The effect of fenfluramine on the pulmonary disposition of 5-hydroxytryptamine in the isolated perfused rat lung: a comparison with chlorphentermine.
2000 Jan
Anorexigen-induced pulmonary hypertension and the serotonin (5-HT) hypothesis: lessons for the future in pathogenesis.
2002
Screening for amphetamine and amphetamine-type drugs in doping analysis by liquid chromatography/mass spectrometry.
2006
Successful drug development despite adverse preclinical findings part 2: examples.
2010 Dec
Insight into human alveolar macrophage and M. tuberculosis interactions via metabolic reconstructions.
2010 Oct 19
Patents

Patents

Sample Use Guides

Adults: 65 mg (one tablet) taken with or shortly after the first meal of the day.
Route of Administration: Oral
In Vitro Use Guide
In contrast, lymphocytes pre-incubated with 10(-5)M chlorphentermine (CP) for 60 min, then stimulated with Con A for 2 hours in the presence of 10(-5)M CP, exhibit a significantly depressed inositol phosphate formation. In addition, CP also inhibited the activity of phospholipase C (IC50 = 0.58 mM), the enzyme responsible for the formation of inositol phosphates during lymphocyte activation. Further, lymphocytes activated in a manner that bypasses the phosphatidylinositol pathway are not inhibited by 10(-7)M or 10(-9)M CP as are cells activated with Con A.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:01:26 GMT 2023
Edited
by admin
on Fri Dec 15 15:01:26 GMT 2023
Record UNII
RL11HOJ7DM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORPHENTERMINE HYDROCHLORIDE
MART.   MI   ORANGE BOOK   USAN   WHO-DD  
USAN  
Official Name English
CHLORPHENTERMINE HYDROCHLORIDE [USAN]
Common Name English
CHLORPHENTERMINE HCL
Common Name English
Chlorphentermine hydrochloride [WHO-DD]
Common Name English
P-CHLORO-.ALPHA.,.ALPHA.-DIMETHYLPHENETHYLAMINE HYDROCHLORIDE
Common Name English
NSC-76098
Code English
CHLORPHENTERMINE HYDROCHLORIDE [MI]
Common Name English
S-62
Code English
PRE-SATE
Brand Name English
W-2426
Code English
BENZENEETHANAMINE, 4-CHLORO-.ALPHA.,.ALPHA.-DIMETHYL-, HYDROCHLORIDE
Systematic Name English
CHLORPHENTERMINE HYDROCHLORIDE [ORANGE BOOK]
Common Name English
CHLORPHENTERMINE HYDROCHLORIDE [MART.]
Common Name English
W 2426
Code English
Classification Tree Code System Code
NCI_THESAURUS C47795
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
DEA NO. 1645
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
Code System Code Type Description
FDA UNII
RL11HOJ7DM
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
NSC
76098
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
EPA CompTox
DTXSID1047815
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
NCI_THESAURUS
C65324
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
ECHA (EC/EINECS)
205-782-9
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
MERCK INDEX
m3458
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY Merck Index
PUBCHEM
65477
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
ChEMBL
CHEMBL1201269
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
SMS_ID
100000084738
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
DRUG BANK
DBSALT000815
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
EVMPD
SUB01251MIG
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
CAS
151-06-4
Created by admin on Fri Dec 15 15:01:26 GMT 2023 , Edited by admin on Fri Dec 15 15:01:26 GMT 2023
PRIMARY
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