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

Details

Stereochemistry RACEMIC
Molecular Formula C17H14O3S
Molecular Weight 298.356
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ZALTOPROFEN

SMILES

CC(C(O)=O)C1=CC=C2SC3=CC=CC=C3C(=O)CC2=C1

InChI

InChIKey=MUXFZBHBYYYLTH-UHFFFAOYSA-N
InChI=1S/C17H14O3S/c1-10(17(19)20)11-6-7-15-12(8-11)9-14(18)13-4-2-3-5-16(13)21-15/h2-8,10H,9H2,1H3,(H,19,20)

HIDE SMILES / InChI

Molecular Formula C17H14O3S
Molecular Weight 298.356
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, http://www.ncbi.nlm.nih.gov/pubmed/16473424

Zaltoprofen is a non-steroidal anti-inflammatory drug approved in Japan for the treatment of lumbar pain, frozen shoulder, osteoarthritis, musculoskeletal pain, dental pain, post-operative pain. The main mechanism of action involves the inhibition of COX-2. Additional mechanism may be associated with the inhibitory effect of zaltoprofen on bradykinin-induced nociceptive responses that happens without blocking bradykinin receptors.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P35354
Gene ID: 5743.0
Gene Symbol: PTGS2
Target Organism: Homo sapiens (Human)
Sources: www.ncbi.nlm.nih.gov/pubmed/12065695
0.34 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
SOLETON

Approved Use

It is usually used for anti-inflammation and analgesia in rheumatoid arthritis, osteoarthritis, low back pain, shoulder periarthritis, cervicobrachial syndrome as well as pain after operation, injuries or tooth removal.
Palliative
SOLETON

Approved Use

It is usually used for anti-inflammation and analgesia in rheumatoid arthritis, osteoarthritis, low back pain, shoulder periarthritis, cervicobrachial syndrome as well as pain after operation, injuries or tooth removal.
Palliative
SOLETON

Approved Use

It is usually used for anti-inflammation and analgesia in rheumatoid arthritis, osteoarthritis, low back pain, shoulder periarthritis, cervicobrachial syndrome as well as pain after operation, injuries or tooth removal.
Palliative
SOLETON

Approved Use

It is usually used for anti-inflammation and analgesia in rheumatoid arthritis, osteoarthritis, low back pain, shoulder periarthritis, cervicobrachial syndrome as well as pain after operation, injuries or tooth removal.
Primary
SOLETON

Approved Use

It is usually used for anti-inflammation and analgesia in rheumatoid arthritis, osteoarthritis, low back pain, shoulder periarthritis, cervicobrachial syndrome as well as pain after operation, injuries or tooth removal.
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
5 μg/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
5.37 μg/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
12.32 μg/mL
160 mg single, oral
dose: 160 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
16.41 μg/mL
240 mg single, oral
dose: 240 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
4.9 μg/mL
80 mg 3 times / day steady-state, oral
dose: 80 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
4.85 μg/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
4.46 μg/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
3.71 μg/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
3.52 μg/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
12.77 μg × h/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
15.57 μg × h/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
41.61 μg × h/mL
160 mg single, oral
dose: 160 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
53.41 μg × h/mL
240 mg single, oral
dose: 240 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
16.54 μg × h/mL
80 mg 3 times / day steady-state, oral
dose: 80 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
19.66 μg × h/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
20.35 μg × h/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
20.14 μg × h/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
20.09 μg × h/mL
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
9.08 h
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
4.83 h
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
5.04 h
160 mg single, oral
dose: 160 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
4.83 h
240 mg single, oral
dose: 240 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
6.49 h
80 mg 3 times / day steady-state, oral
dose: 80 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
4.89 h
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
4.95 h
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
4.89 h
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
4.87 h
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FED
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
2%
80 mg single, oral
dose: 80 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
ZALTOPROFEN plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
100 mg 3 times / day multiple, oral
Highest studied dose
Dose: 100 mg, 3 times / day
Route: oral
Route: multiple
Dose: 100 mg, 3 times / day
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M
Food Status: UNKNOWN
Sources:
300 mg single, oral
Highest studied dose
Dose: 300 mg
Route: oral
Route: single
Dose: 300 mg
Sources:
healthy, ADULT
Health Status: healthy
Age Group: ADULT
Sex: M
Food Status: FASTED
Sources:
PubMed

PubMed

TitleDatePubMed
Preemptive analgesia by zaltoprofen that inhibits bradykinin action and cyclooxygenase in a post-operative pain model.
2005-04
Patents

Sample Use Guides

In general, for adults, take 1 tablet (80 mg of the active ingredient) at a time, 3 times a day. If the medicine is taken as needed, take 1 to 2 tablets (80 mg to 160 mg) at a time.
Route of Administration: Oral
In Vitro Use Guide
Sources: www.ncbi.nlm.nih.gov/pubmed/12065695
The proliferation of rheumatoid synovial cells was studied after incubation with zaltoprofen (300 uM). IC50 value for inhibition of cell viability was 135.2 uM. Zaltoprofen suppressedthecellproliferationin a concentration-dependent manner, with IC50 value of 48.9 uM.
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:30:26 GMT 2025
Edited
by admin
on Mon Mar 31 18:30:26 GMT 2025
Record UNII
H8635NG3PY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ZALTOPROFEN
INN   MART.   MI   WHO-DD  
INN  
Official Name English
PEON
Preferred Name English
SORETON
Brand Name English
CN-100
Code English
ZALTOPROFEN [MI]
Common Name English
ZALTOPROFEN [MART.]
Common Name English
ZALTOPROFEN [JAN]
Common Name English
Zaltoprofen [WHO-DD]
Common Name English
zaltoprofen [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
Code System Code Type Description
FDA UNII
H8635NG3PY
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
277-973-5
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
WIKIPEDIA
Zaltoprofen
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
ChEMBL
CHEMBL1765291
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
CAS
89482-00-8
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
SUPERSEDED
NCI_THESAURUS
C66681
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
INN
6703
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
DRUG BANK
DB06737
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
EVMPD
SUB00135MIG
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
MERCK INDEX
m11580
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY Merck Index
DRUG CENTRAL
2858
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
SMS_ID
100000079388
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
CAS
74711-43-6
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
PUBCHEM
5720
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID0049076
Created by admin on Mon Mar 31 18:30:26 GMT 2025 , Edited by admin on Mon Mar 31 18:30:26 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY