Ramatroban

Ramatroban

SCHEMBL29031

O=C(O)CCn1c2c(c3ccccc31)CC(NS(=O)(=O)c1ccc(F)cc1)CC2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGDR2TBXA2R

The experimentally established mechanism targets of Ramatroban. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
PTGDR2 known ✓ Q9Y5Y4 18/20 1.00
TBXA2R known ✓ P21731 8/20 1.00
PTGDR Q13258 6/20 1.00
ABCB11 O95342 1/20 1.00
CYP2C9 P11712 1/20 1.00
DRD1 P21728 1/20 1.00
CCKAR P32238 1/20 1.00
KDM4E B2RXH2 1/20 0.51
ALDH1A1 P00352 1/20 0.51
RB1 P06400 1/20 0.48

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Ramatroban SCHEMBL29030 1.00 PTGDR2 (1.00) PTGDR2TBXA2RPTGDRABCB11CYP2C9
Ramatroban SCHEMBL20769768 1.00 PTGDR2 (1.00) PTGDR2TBXA2RPTGDRABCB11CYP2C9
Ramatroban SCHEMBL29503087 1.00 PTGDR2 (1.00) PTGDR2TBXA2RPTGDRABCB11CYP2C9
Ramatroban SCHEMBL1427851 1.00 PTGDR2 (1.00) PTGDR2TBXA2RPTGDRABCB11CYP2C9
Ramatroban SCHEMBL1427848 0.99 PTGDR2 (0.98) PTGDR2TBXA2RPTGDRABCB11CYP2C9
Ramatroban SCHEMBL1427850 0.99 PTGDR2 (0.98) PTGDR2TBXA2RPTGDRABCB11CYP2C9
SCHEMBL9442771 0.95 PTGDR2 (0.90) PTGDR2TBXA2RPTGDRABCB11CYP2C9
SCHEMBL9833660 0.93 PTGDR2 (0.87) PTGDR2TBXA2RPTGDRABCB11CYP2C9
Ramatroban SCHEMBL1427849 0.92 PTGDR2 (0.85) PTGDR2TBXA2RPTGDRABCB11CYP2C9
SCHEMBL9429657 0.92 PTGDR2 (0.85) PTGDR2TBXA2RPTGDRABCB11CYP2C9

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Appears in 3515 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250228844-A1 SINGLE NUCLEOTIDE POLYMORPHIC ALLELES OF HUMAN DP-2 GENE FOR DETECTION OF SUSCEPTIBILITY TO HAIR GROWTH INHIBITION BY PGD2 THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2025-07-17 US claimed
CN-120154601-A Application of ramatrum Ban Zaizhi in preparation of medicine for preventing or treating radioactive esophageal injury caused by ionizing radiation 核工业四一六医院 2025-06-17 CN claimed
US-20250144079-A1 METHODS OF INHIBITING TUMOR METASTASIS VANDERBILT UNIVERSITY 2025-05-08 US claimed
US-12201625-B2 Single nucleotide polymorphic alleles of human DP-2 gene for detection of susceptibility to hair growth inhibition by PGD2 THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2025-01-21 US claimed
CN-112368300-B SPNS2 neutralizing antibodies 帝人制药株式会社 2024-10-01 CN claimed
US-20240216380-A1 BTK Inhibitors to Treat Solid Tumors Through Modulation of the Tumor Microenvironment ACERTA PHARMA BV (NL) 2024-07-04 US claimed
US-20240180904-A1 Methods of Treating Chronic Lymphocytic Leukemia and Small Lymphocytic Leukemia Using a BTK Inhibitor ACERTA PHARMA BV (NL) 2024-06-06 US claimed
US-20240041839-A1 METHODS OF INHIBITING TUMOR METASTASIS VANDERBILT UNIVERSITY 2024-02-08 US claimed
US-20230414575-A1 MK2 ACTIVATING COMPOUNDS FOR USE IN TREATING VASCULAR LEAK AND ENDOTHELIAL BARRIER DISORDERS AKTTYVA THERAPEUTICS INC (US) 2023-12-28 US claimed
CN-117122687-A Methods for inhibiting tumor metastasis 凡德贝尔大学 2023-11-28 CN claimed
CN-1282320-A Thermodynamically stable form of -3- [ [ (4-fluorophenyl) sulfonyl ] amino ] -1, 2,3, 4-tetrahydro-9H-carbazole-9-propanoic acid (ramatroban) BAYER YAKUHIN LTD (JP) 2001-01-31 CN claimed
EP-1051398-A1 THERMODYNAMICALLY STABLE FORM OF (R)-3- (4-FLUOROPHENYL) SULPHONYL]AMINO] -1,2,3,4- TETRAHYDRO -9H-CARBAZOLE -9-PROPANOIC ACID (RAMATROBAN) BAYER YAKUHIN LTD. (JP) 2000-11-15 EP claimed
WO-1999033803-A1 THERMODYNAMICALLY STABLE FORM OF (R)-3-[ [(4-FLUOROPHENYL) SULPHONYL]AMINO] -1,2,3,4- TETRAHYDRO -9H-CARBAZOLE -9-PROPANOIC ACID (RAMATROBAN) BAYER YAKUHIN, LTD. (JP) 1999-07-08 WO claimed
US-5462726-A Suppressing vasoconstriction BRISTOL-MYERS SQUIBB COMPANY (US) 1995-10-31 US claimed
US-5204121-A Active material core, double layer comprising outer acrylic layer and inner jacket of hydrophobic additive and hydroxy-propyl cellulose BAYER AKTIENGESELLSCHAFT (DE) 1993-04-20 US claimed
EP-0386440-B1 MEDICAMENT WITH CONTROLLED RELEASE OF THE ACTIVE INGREDIENT BAYER AG (DE) 1992-08-05 EP claimed
EP-0448274-A2 Use of a thromboxane A2 receptor antagonist for the manufacture of a medicament for the treatment of ulcerative gastrointestinal conditions E.R. SQUIBB & SONS, INC. (US) 1991-09-25 EP claimed
EP-0242518-B1 Cycloalkano[1,2-b]indole-sulfonamides BAYER AG (DE) 1991-04-10 EP claimed
US-4965258-A Anticoagulant; thromboxane a2 antagonist BAYER AKTIENGESELLSCHAFT (DE) 1990-10-23 US claimed
EP-0242518-A1 Cycloalkano[1,2-b]indole-sulfonamides BAYER AG (DE) 1987-10-28 EP claimed