SCHEMBL1255151

SCHEMBL1255151

C[C@@H](c1ccc(Cl)cc1)n1c2c(c3cc(F)cc(S(C)(=O)=O)c31)CCC[C@@H]2CC(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
PTGDR Q13258 19/20 1.00
TBXA2R P21731 14/20 1.00
PDE2A O00408 6/20 1.00
PTGER1 P34995 1/20 0.82
PTGER4 P35408 1/20 0.82
PTGFR P43088 1/20 0.82
PTGER3 P43115 1/20 0.82
PTGER2 P43116 1/20 0.82
PTGIR P43119 1/20 0.82

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
SCHEMBL5824247 1.00 PTGDR (1.00) PTGDRTBXA2RPDE2APTGER1PTGER4
SCHEMBL20531411 1.00 PTGDR (1.00) PTGDRTBXA2RPDE2APTGER1PTGER4
SCHEMBL1255195 1.00 PTGDR (1.00) PTGDRTBXA2RPDE2APTGER1PTGER4
SCHEMBL6521839 1.00 PTGDR (1.00) PTGDRTBXA2RPDE2APTGER1PTGER4
SCHEMBL1043387 0.95 PTGDR (0.90) PTGDRTBXA2RPDE2APTGER1PTGER4
SCHEMBL20531485 0.95 PTGDR (0.90) PTGDRTBXA2RPDE2APTGER1PTGER4
SCHEMBL5421906 0.95 PTGDR (0.90) PTGDRTBXA2RPDE2APTGER1PTGER4
SCHEMBL990414 0.95 PTGDR (1.00) PTGDRTBXA2RPDE2APTGER1PTGER4
SCHEMBL6097496 0.92 PTGDR (1.00) PTGDRTBXA2RPDE2APTGER1PTGER4
SCHEMBL989833 0.92 PTGDR (1.00) PTGDRTBXA2RPDE2APTGER1PTGER4

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

Claimed or disclosed in 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070054951-A1 Fluoro-methanesulfonyl-substituted cycloalkanoindoles and their use as prostaglandin D2 antagonists MERCK FROSST CANADA & CO. (CA) 2007-03-08 US claimed
US-12589089-B2 PTGDR-1 and/or PTGDR-2 antagonists for preventing and/or treating systemic lupus erythematosus INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE) (FR) 2026-03-31 US disclosed
US-20250017900-A1 PTGDR-1 AND/OR PTGDR-2 ANTAGONISTS FOR PREVENTING AND/OR TREATING SYSTEMIC LUPUS ERYTHEMATOSUS UNIVERSITÉ PARIS CITÉ (FR) 2025-01-16 US disclosed
EP-2116244-B1 Method of treating atherosclerosis, dyslipidemias and related conditions SCHERING CORP (US) 2012-08-08 EP disclosed
US-20110118292-A1 METHOD OF TREATING ATHEROSCLEROSIS, DYSLIPIDEMIAS AND RELATED CONDITIONS CHENG KANG 2011-05-19 US disclosed
EP-2286816-A1 Method of treating atherosclerosis, dyslipidemias and related conditions MERCK SHARP & DOHME (I.A.) CORP. (US) 2011-02-23 EP disclosed
US-20100076002-A1 Method of Treating Atherosclerosis, Dyslipidemias and Related Conditions and Pharmaceutical Compositions CHENG KANG 2010-03-25 US disclosed
EP-2116244-A1 Method of treating atherosclerosis, dyslipidemias and related conditions Merck & Co., Inc. (US) 2009-11-11 EP disclosed
US-20090233977-A1 Method of Treating Atherosclerosis, dyslipidemias and related conditions MERCK SHARP & DOHME CORP. 2009-09-17 US disclosed
EP-1809284-A4 NIACIN RECEPTOR AGONISTS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT MERCK & CO INC (US) 2009-09-09 EP disclosed
US-20070244107-A1 Method of Treating Atherosclerosis, Dyslipidemias and Related Conditions MERCK & CO., INC. 2007-10-18 US disclosed
EP-1809284-A2 NIACIN RECEPTOR AGONISTS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT Merck & Co., Inc. (US) 2007-07-25 EP disclosed
US-20070054951-A1 Fluoro-methanesulfonyl-substituted cycloalkanoindoles and their use as prostaglandin D2 antagonists MERCK FROSST CANADA & CO. (CA) 2007-03-08 US disclosed
US-20070054951-A1 Fluoro-methanesulfonyl-substituted cycloalkanoindoles and their use as prostaglandin D2 antagonists MERCK FROSST CANADA & CO. (CA) 2007-03-08 US disclosed
US-20070054951-A1 Fluoro-methanesulfonyl-substituted cycloalkanoindoles and their use as prostaglandin D2 antagonists MERCK FROSST CANADA & CO. (CA) 2007-03-08 US disclosed
WO-2006052555-A2 NIACIN RECEPTOR AGONISTS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT MERCK & CO., INC. (US) 2006-05-18 WO disclosed
WO-2006052798-A2 METHOD OF TREATING PATHOLOGICAL BLUSHING MERCK & CO., INC. (US) 2006-05-18 WO disclosed
US-7019022-B2 Substituted tetrahydrocarbazole and cyclopentanoindole derivatives MERCK FROSST CANADA & CO. (CA) 2006-03-28 US disclosed
US-20050154044-A1 Substituted tetrahydrocarbazole and cyclopentanoindole derivatives MERCK FROSST CANADA LTD. (CA) 2005-07-14 US disclosed
US-20040229844-A1 Method of treating atherosclerosis, dyslipidemias and related conditions CHENG KANG (US) 2004-11-18 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (9 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20250017900-A1 PTGDR-1 AND/OR PTGDR-2 ANTAGONISTS FOR PREVENTING AND/OR TREATING SYSTEMIC LUPUS ERYTHEMATOSUS PTGDR, PTGDR2, PTGIR PTGDR 1/4885TBXA2R 16/4885PDE2A 223/4885
US-20100076002-A1 Method of Treating Atherosclerosis, Dyslipidemias and Related Conditions and Pharmaceutical Compositions LDLR, LPAR5, FFAR1 PTGDR 164/4885TBXA2R 44/4885PDE2A 813/4885
US-20070054951-A1 Fluoro-methanesulfonyl-substituted cycloalkanoindoles and their use as prostaglandin D2 antagonists PTGDR2, PTGER2, PTGDR PTGDR 3/4885TBXA2R 18/4885PDE2A 295/4885
US-20090233977-A1 Method of Treating Atherosclerosis, dyslipidemias and related conditions LDLR, HCAR1, FFAR1 PTGDR 201/4885TBXA2R 37/4885PDE2A 1108/4885
US-12589089-B2 PTGDR-1 and/or PTGDR-2 antagonists for preventing and/or treating systemic lupus erythematosus PTGIR, PTGDR, SSB PTGDR 2/4885TBXA2R 13/4885PDE2A 346/4885
US-20070244107-A1 Method of Treating Atherosclerosis, Dyslipidemias and Related Conditions LDLR, LIPA, APOB PTGDR 97/4885TBXA2R 68/4885PDE2A 1070/4885
US-20050154044-A1 Substituted tetrahydrocarbazole and cyclopentanoindole derivatives PTGIR, PTGDR, PTGDR2 PTGDR 2/4885TBXA2R 10/4885PDE2A 1080/4885
US-20110118292-A1 METHOD OF TREATING ATHEROSCLEROSIS, DYSLIPIDEMIAS AND RELATED CONDITIONS LDLR, HCAR1, FFAR1 PTGDR 201/4885TBXA2R 37/4885PDE2A 1108/4885
US-20040229844-A1 Method of treating atherosclerosis, dyslipidemias and related conditions LDLR, HCAR1, FFAR1 PTGDR 201/4885TBXA2R 37/4885PDE2A 1108/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.