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Details

Stereochemistry UNKNOWN
Molecular Formula C21H21FN2O4S
Molecular Weight 416.466
Optical Activity ( + )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAY-10471

SMILES

CN(C1CCC2=C(C1)C3=CC=CC=C3N2CC(O)=O)S(=O)(=O)C4=CC=C(F)C=C4

InChI

InChIKey=CANCTKXGRVNXFP-UHFFFAOYSA-N
InChI=1S/C21H21FN2O4S/c1-23(29(27,28)16-9-6-14(22)7-10-16)15-8-11-20-18(12-15)17-4-2-3-5-19(17)24(20)13-21(25)26/h2-7,9-10,15H,8,11-13H2,1H3,(H,25,26)

HIDE SMILES / InChI

Molecular Formula C21H21FN2O4S
Molecular Weight 416.466
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/16418339

TM30089 is a slective CRTH2 antagonist. TM30089, displayed high selectivity for and antagonistic potency on mouse CRTH2 but lacked affinity to TP and many other receptors including the related anaphylatoxin C3a and C5a receptors, selected chemokine receptors and the cyclooxygenase isoforms 1 and 2 which are all recognized players in allergic diseases. Furthermore, TM30089 and ramatroban, the latter used as a reference herein, similarly inhibited asthma pathology in vivo by reducing peribronchial eosinophilia and mucus cell hyperplasia.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
3.6 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Antagonism of the prostaglandin D2 receptor CRTH2 attenuates asthma pathology in mouse eosinophilic airway inflammation.
2007 Feb 28
PGH1, the precursor for the anti-inflammatory prostaglandins of the 1-series, is a potent activator of the pro-inflammatory receptor CRTH2/DP2.
2012
Patents

Sample Use Guides

Mice: mice were treated twice daily with TM30089 (5 mg/kg orally)
Route of Administration: Oral
1 uM of TM30089 inhibited chemotactic activation of human eosinophils, measured in eosinophil shape change assays.
Substance Class Chemical
Created
by admin
on Sat Dec 16 18:18:46 GMT 2023
Edited
by admin
on Sat Dec 16 18:18:46 GMT 2023
Record UNII
F449K9EB2G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAY-10471
Code English
(+)-3-[[(4-Fluorophenyl)sulfonyl]methylamino]-1,2,3,4-tetrahydro-9H-carbazole-9-acetic acid
Systematic Name English
TM30089
Code English
TM-30089
Code English
CAY10471
Code English
9H-Carbazole-9-acetic acid, 3-[[(4-fluorophenyl)sulfonyl]methylamino]-1,2,3,4-tetrahydro-, (+)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID00722396
Created by admin on Sat Dec 16 18:18:46 GMT 2023 , Edited by admin on Sat Dec 16 18:18:46 GMT 2023
PRIMARY
PUBCHEM
11384493
Created by admin on Sat Dec 16 18:18:46 GMT 2023 , Edited by admin on Sat Dec 16 18:18:46 GMT 2023
PRIMARY
CAS
627865-18-3
Created by admin on Sat Dec 16 18:18:46 GMT 2023 , Edited by admin on Sat Dec 16 18:18:46 GMT 2023
PRIMARY
FDA UNII
F449K9EB2G
Created by admin on Sat Dec 16 18:18:46 GMT 2023 , Edited by admin on Sat Dec 16 18:18:46 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY