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

Details

Stereochemistry RACEMIC
Molecular Formula C17H22N2O
Molecular Weight 270.3694
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DOXYLAMINE

SMILES

CN(C)CCOC(C)(C1=CC=CC=C1)C2=CC=CC=N2

InChI

InChIKey=HCFDWZZGGLSKEP-UHFFFAOYSA-N
InChI=1S/C17H22N2O/c1-17(20-14-13-19(2)3,15-9-5-4-6-10-15)16-11-7-8-12-18-16/h4-12H,13-14H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C17H22N2O
Molecular Weight 270.3694
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.drugs.com/cdi/doxylamine.html

Doxylamine is an antihistamine commonly used as a sleep aid. This drug is also used to relieve symptoms of hay fever (allergic rhinitis), hives (rash or itching), and other allergic reactions. Doxylamine is a member of the ethanolamine class of antihistamines and has anti-allergy power far superior to virtually every other antihistamine on the market, with the exception of diphenhydramine (Benadryl). It is also the most powerful over-the-counter sedative available in the United States, and more sedating than many prescription hypnotics. In a study, it was found to be superior to even the barbiturate, phenobarbital for use as a sedative. Doxylamine is also a potent anticholinergic. Like other antihistamines, doxylamine acts by competitively inhibiting histamine at H1 receptors. It also has substantial sedative and anticholinergic effects. Used alone as a short-term sleep aid, in combination with other drugs as a night-time cold and allergy relief drug. Also used in combination with Vitamin B6 (pyridoxine) to prevent morning sickness in pregnant women.

CNS Activity

Curator's Comment: Penetrating into the central nervous system, the drug has a marked sedative effect, promoting sleep.

Originator

Curator's Comment: Bendectin (DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE) was introduced in 1957 by Merrell Dow Pharmaceuticals

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
42.0 nM [Ki]
200.0 nM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unisom

Approved Use

Allergic rhinitis or other respiratory allergies (oral liquid only): Temporary relief of rhinorrhea, sneezing, itchy nose or throat, and itchy, watery eyes due to hay fever or other respiratory allergies Insomnia (tablets only): Reduce difficulty falling asleep

Launch Date

1978
Primary
Unisom

Approved Use

Allergic rhinitis or other respiratory allergies (oral liquid only): Temporary relief of rhinorrhea, sneezing, itchy nose or throat, and itchy, watery eyes due to hay fever or other respiratory allergies Insomnia (tablets only): Reduce difficulty falling asleep

Launch Date

1978
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
61.94 ng/mL
12.5 mg single, oral
dose: 12.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
124.91 ng/mL
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
12.9 ng/mL
3.2 mg single, nasal
dose: 3.2 mg
route of administration: Nasal
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
18.9 ng/mL
6.3 mg single, nasal
dose: 6.3 mg
route of administration: Nasal
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
27.1 ng/mL
12.7 mg single, nasal
dose: 12.7 mg
route of administration: Nasal
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
142 ng/mL
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
99 ng/mL
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
83.3 ng/mL
20 mg single, oral
dose: 20 mg
route of administration: Oral
experiment type: SINGLE
co-administered: PYRIDOXINE HYDROCHLORIDE
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
168.6 ng/mL
40 mg 1 times / day multiple, oral
dose: 40 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered: PYRIDOXINE HYDROCHLORIDE
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
859.74 ng × h/mL
12.5 mg single, oral
dose: 12.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
1697.58 ng × h/mL
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
81.1 ng × h/mL
3.2 mg single, nasal
dose: 3.2 mg
route of administration: Nasal
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
117.7 ng × h/mL
6.3 mg single, nasal
dose: 6.3 mg
route of administration: Nasal
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
161.8 ng × h/mL
12.7 mg single, nasal
dose: 12.7 mg
route of administration: Nasal
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
751.8 ng × h/mL
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
1280.9 ng × h/mL
20 mg single, oral
dose: 20 mg
route of administration: Oral
experiment type: SINGLE
co-administered: PYRIDOXINE HYDROCHLORIDE
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
3721.5 ng × h/mL
40 mg 1 times / day multiple, oral
dose: 40 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered: PYRIDOXINE HYDROCHLORIDE
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
12.23 h
12.5 mg single, oral
dose: 12.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
12.45 h
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
10.2 h
3.2 mg single, nasal
dose: 3.2 mg
route of administration: Nasal
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
11.8 h
6.3 mg single, nasal
dose: 6.3 mg
route of administration: Nasal
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
10.1 h
12.7 mg single, nasal
dose: 12.7 mg
route of administration: Nasal
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
10.4 h
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
10.1 h
25 mg single, oral
dose: 25 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
10.1 h
20 mg single, oral
dose: 20 mg
route of administration: Oral
experiment type: SINGLE
co-administered: PYRIDOXINE HYDROCHLORIDE
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
11.9 h
40 mg 1 times / day multiple, oral
dose: 40 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered: PYRIDOXINE HYDROCHLORIDE
DOXYLAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
150 mg single, oral
Overdose
Dose: 150 mg
Route: oral
Route: single
Dose: 150 mg
Sources:
unknown, 2
Health Status: unknown
Age Group: 2
Sex: M
Sources:
Other AEs: Agitation, Dilated pupils...
Other AEs:
Agitation
Dilated pupils
Sources:
25 mg single, oral
Studied dose
Dose: 25 mg
Route: oral
Route: single
Dose: 25 mg
Sources:
healthy, 28 - 58
Health Status: healthy
Age Group: 28 - 58
Sex: M+F
Sources:
Other AEs: Somnolence...
Other AEs:
Somnolence (50%)
Sources:
12.7 mg single, intranasal
Highest studied dose
Dose: 12.7 mg
Route: intranasal
Route: single
Dose: 12.7 mg
Sources:
unhealthy, 35.9 (8.00)
Health Status: unhealthy
Age Group: 35.9 (8.00)
Sex: M+F
Sources:
13 mg/kg single, oral
Overdose
Dose: 13 mg/kg
Route: oral
Route: single
Dose: 13 mg/kg
Sources:
unknown
Health Status: unknown
Sources:
Other AEs: Rhabdomyolysis...
Other AEs:
Rhabdomyolysis
Sources:
20 mg 2 times / day multiple, oral
Recommended
Dose: 20 mg, 2 times / day
Route: oral
Route: multiple
Dose: 20 mg, 2 times / day
Sources:
unhealthy
Other AEs: Somnolence...
20 mg 2 times / day multiple, oral
Recommended
Dose: 20 mg, 2 times / day
Route: oral
Route: multiple
Dose: 20 mg, 2 times / day
Sources:
unhealthy
Other AEs: Drowsiness...
20 mg single, oral
Recommended
Dose: 20 mg
Route: oral
Route: single
Dose: 20 mg
Sources:
healthy
Disc. AE: Vomiting...
AEs leading to
discontinuation/dose reduction:
Vomiting
Sources:
20 mg 2 times / day steady, oral
Recommended
Dose: 20 mg, 2 times / day
Route: oral
Route: steady
Dose: 20 mg, 2 times / day
Sources:
healthy
Disc. AE: Vomiting, Decreased hemoglobin...
AEs leading to
discontinuation/dose reduction:
Vomiting
Decreased hemoglobin
Visual impairment
Sources:
AEs

AEs

AESignificanceDosePopulation
Agitation
150 mg single, oral
Overdose
Dose: 150 mg
Route: oral
Route: single
Dose: 150 mg
Sources:
unknown, 2
Health Status: unknown
Age Group: 2
Sex: M
Sources:
Dilated pupils
150 mg single, oral
Overdose
Dose: 150 mg
Route: oral
Route: single
Dose: 150 mg
Sources:
unknown, 2
Health Status: unknown
Age Group: 2
Sex: M
Sources:
Somnolence 50%
25 mg single, oral
Studied dose
Dose: 25 mg
Route: oral
Route: single
Dose: 25 mg
Sources:
healthy, 28 - 58
Health Status: healthy
Age Group: 28 - 58
Sex: M+F
Sources:
Rhabdomyolysis
13 mg/kg single, oral
Overdose
Dose: 13 mg/kg
Route: oral
Route: single
Dose: 13 mg/kg
Sources:
unknown
Health Status: unknown
Sources:
Somnolence
20 mg 2 times / day multiple, oral
Recommended
Dose: 20 mg, 2 times / day
Route: oral
Route: multiple
Dose: 20 mg, 2 times / day
Sources:
unhealthy
Drowsiness grade 3
20 mg 2 times / day multiple, oral
Recommended
Dose: 20 mg, 2 times / day
Route: oral
Route: multiple
Dose: 20 mg, 2 times / day
Sources:
unhealthy
Vomiting Disc. AE
20 mg single, oral
Recommended
Dose: 20 mg
Route: oral
Route: single
Dose: 20 mg
Sources:
healthy
Decreased hemoglobin Disc. AE
20 mg 2 times / day steady, oral
Recommended
Dose: 20 mg, 2 times / day
Route: oral
Route: steady
Dose: 20 mg, 2 times / day
Sources:
healthy
Visual impairment Disc. AE
20 mg 2 times / day steady, oral
Recommended
Dose: 20 mg, 2 times / day
Route: oral
Route: steady
Dose: 20 mg, 2 times / day
Sources:
healthy
Vomiting Disc. AE
20 mg 2 times / day steady, oral
Recommended
Dose: 20 mg, 2 times / day
Route: oral
Route: steady
Dose: 20 mg, 2 times / day
Sources:
healthy
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer





Drug as perpetrator​
PubMed

PubMed

TitleDatePubMed
Rational quantitative structure-activity relationship (RQSAR) screen for PXR and CAR isoform-specific nuclear receptor ligands.
2010-12-05
Effectiveness of delayed-release doxylamine and pyridoxine for nausea and vomiting of pregnancy: a randomized placebo controlled trial.
2010-12
An unusual death involving a sensory deprivation tank.
2010-11
Clinical practice. Nausea and vomiting in pregnancy.
2010-10-14
An overdose death involving the insufflation of extended-release oxymorphone tablets.
2010-10
Commonly prescribed medications and potential false-positive urine drug screens.
2010-08-15
Optimal management of nausea and vomiting of pregnancy.
2010-08-04
Learning curves for pediatric laparoscopy: how many operations are enough? The Amsterdam experience with laparoscopic pyloromyotomy.
2010-08
Managing hyperemesis gravidarum: a multimodal challenge.
2010-07-15
[Hyperemesis gravidarum: a rare but potentially severe complication of the first trimester of pregnancy].
2010-06-20
Biotransformation of ginsenosides Rb1, Rg3 and Rh2 in rat gastrointestinal tracts.
2010-05-26
Multiple-drug toxicity caused by the coadministration of 4-methylmethcathinone (mephedrone) and heroin.
2010-04
A tendency for re-offending in drug-facilitated crime.
2010-03-20
Authenticity of claims made in drug promotional literature.
2010-02
Does advice from pharmacy staff vary according to the nonprescription medicine requested?
2009-11
Drugs associated with more suicidal ideations are also associated with more suicide attempts.
2009-10-02
Acute renal failure caused by pheniramine maleate induced rhabdomyolysis: an unusual case.
2009-10
Extended suicide using an atypical stud gun.
2009-08-10
Comparison of chiral separation of basic drugs in capillary electrophoresis and liquid chromatography using neutral and negatively charged cyclodextrins.
2009-07-10
Long-term neurodevelopment of children exposed to maternal nausea and vomiting of pregnancy and diclectin.
2009-07
The identification of ingested dandelion juice in gastric contents of a deceased person by direct sequencing and GC-MS methods.
2009-05
Doxylamine toxicity: seizure, rhabdomyolysis and false positive urine drug screen for methadone.
2009
Pharmacokinetic comparison of a delayed-release combination of doxylamine succinate and pyridoxine hydrocholoride (Diclectin) and oral solutions of these drugs in healthy women of childbearing age.
2009
A thyrotoxicosis outbreak due to dietary pills in Paris.
2008-12
"DXemon juice:" analytical evaluation of an extraction process for the purification and freebasing of dextromethorphan from cold preparations.
2008-12
Simultaneous determination of a ternary mixture of doxylamine succinate, pyridoxine hydrochloride, and folic acid by the ratio spectra-zero-crossing, double divisor-ratio spectra derivative, and column high-performance liquid chromatographic methods.
2008-11-05
Sleep complaints: Whenever possible, avoid the use of sleeping pills.
2008-10
[Is good care (only) guaranteed by a specialist?].
2008-04-15
Representation and re-presentation in litigation science.
2008-01
Differentially expressed genes in embryonic cardiac tissues of mice lacking Folr1 gene activity.
2007-11-20
An estimate of the proportion of drug-facilitation of sexual assault in four U.S. localities.
2007-11
Managing nausea and vomiting of pregnancy: a survey of obstetrician-gynecologists.
2007-10
Risk factors for rhabdomyolysis following doxylamine overdose.
2007-08
[Chemicotoxicological evaluation of doxylamine].
2007-06-30
Inactivation of anthracyclines by serum heme proteins.
2007-06
Separation of cold medicine ingredients using a precise MEKC method at elevated pH.
2007-06
OTC product: Zicam Cold and Flu Medicated Spoons.
2007-05-23
First-generation H1 antihistamines found in pilot fatalities of civil aviation accidents, 1990-2005.
2007-05
Characterization of antihistamine-human serum protein interactions by capillary electrophoresis.
2007-04-20
Efficacy of a single evening dose of syrup containing paracetamol, dextromethorphan hydrobromide, doxylamine succinate and ephedrine sulfate in subjects with multiple common cold symptoms.
2007-04
Comparison of lactated Ringer's solution and 0.9% saline in the treatment of rhabdomyolysis induced by doxylamine intoxication.
2007-04
[Transitory acute psychosis with serotoninergic syndrome at the time of an intoxication by dosulepin associated with doxylamine and ethanol].
2007-03-14
Possible role of pseudoephedrine and other over-the-counter cold medications in the deaths of very young children.
2007-03
American Gastroenterological Association institute medical position statement on the use of gastrointestinal medication in pregnancy.
2007-02
The risk of risk reduction: can postmarket surveillance pose more risk than benefit?
2007
Preventing recurrence of severe morning sickness.
2006-12
Vanished behind the counter. Starting this week, you'll need help buying your claritin and nyquil.
2006-10-02
[Juvenile pityriasis rubra pilaris].
2006-10
[Unilateral laterothoracic exanthema].
2006-10
Therapy insight: drugs for gastrointestinal disorders in pregnant women.
2006-05
Patents

Sample Use Guides

In Vivo Use Guide
Usual Adult Dose for Allergic Rhinitis Doxylamine 5 mg oral tablet, chewable: 10 mg orally every 4 to 6 hours not to exceed 6 doses daily. Usual Adult Dose for Allergic Conjunctivitis Doxylamine 5 mg oral tablet, chewable: 10 mg orally every 4 to 6 hours not to exceed 6 doses daily. Usual Adult Dose for Insomnia 12 years of age and older: 25 mg orally 30 minutes before bed
Route of Administration: Oral
In Vitro Use Guide
Doxylamine at 50 ug/ml inhibited both differentiation and proliferation in rat embryo limb bud cell cultures
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:26:51 GMT 2025
Edited
by admin
on Mon Mar 31 21:26:51 GMT 2025
Record UNII
95QB77JKPL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(±)-DOXYLAMINE
Preferred Name English
DOXYLAMINE
HSDB   INN   MI   VANDF   WHO-DD  
INN  
Official Name English
DOXYLAMINE [VANDF]
Common Name English
PYRIDINE, 2-(.ALPHA.-(2-(DIMETHYLAMINO)ETHOXY)-.ALPHA.-METHYLBENZYL)-
Systematic Name English
2-(.ALPHA.(2-(DIMETHYLAMINO)ETHOXY)-.ALPHA.-METHYLBENZYL)PYRIDINE
Systematic Name English
doxylamine [INN]
Common Name English
ETHANAMINE, N,N-DIMETHYL-2-(1-PHENYL-1-(2-PYRIDINYL)ETHOXY)-
Systematic Name English
DOXYLAMINE [MI]
Common Name English
DOXYLAMINE [HSDB]
Common Name English
Doxylamine [WHO-DD]
Common Name English
N,N-DIMETHYL-2-(1-PHENYL-1-(2-PYRIDINYL)ETHOXY)ETHANAMINE
Systematic Name English
Classification Tree Code System Code
WHO-ATC R06AA59
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
CFR 21 CFR 520.784
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
WHO-VATC QR06AA59
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
WHO-ATC R06AA09
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
LIVERTOX NBK548828
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
NCI_THESAURUS C29578
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
NDF-RT N0000175750
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
WHO-VATC QR06AA09
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
Code System Code Type Description
EVMPD
SUB06394MIG
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
DRUG BANK
DB00366
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
FDA UNII
95QB77JKPL
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
IUPHAR
7171
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
DRUG CENTRAL
962
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
NCI_THESAURUS
C61738
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
CHEBI
51380
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
CAS
469-21-6
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-414-2
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
CAS
102737-83-7
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
SUPERSEDED
PUBCHEM
3162
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
MESH
D004319
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
MERCK INDEX
m4759
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID1022970
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
WIKIPEDIA
DOXYLAMINE
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
INN
1782
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
HSDB
5184
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
RXCUI
3642
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY RxNorm
SMS_ID
100000080796
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
LACTMED
Doxylamine
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
DAILYMED
95QB77JKPL
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
ChEMBL
CHEMBL1004
Created by admin on Mon Mar 31 21:26:51 GMT 2025 , Edited by admin on Mon Mar 31 21:26:51 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
ACTIVE ENANTIOMER->RACEMATE
Related Record Type Details
METABOLITE -> PARENT
METABOLITE -> PARENT
Could be free or glucuronide conjugate
URINE
METABOLITE -> PARENT
URINE
METABOLITE -> PARENT
URINE
METABOLITE -> PARENT
METABOLITE -> PARENT
Could be free or glucuronide conjugate
URINE
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC