Diastereomer 2

Diastereomer 2

SCHEMBL1044552

CS(=O)(=O)c1cc(F)cc2c3c(n(Cc4ccc(Cl)cc4)c12)C(CC(=O)O)CC3

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGDR

The experimentally established mechanism targets of Diastereomer 2. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
PTGDR known ✓ Q13258 15/20 1.00
TBXA2R P21731 13/20 1.00
PTGER2 P43116 5/20 1.00
PTGER3 P43115 3/20 1.00
PTGIR P43119 3/20 1.00
PTGER1 P34995 2/20 1.00
PTGFR P43088 2/20 1.00
PDE4A P27815 1/20 1.00
TSPO P30536 1/20 1.00
DRD3 P35462 1/20 1.00
PDE4D Q08499 1/20 1.00
PTGDR2 Q9Y5Y4 1/20 1.00
PDE2A O00408 7/20 0.90
PTGER4 P35408 1/20 0.74

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
Laropiprant SCHEMBL991107 1.00 PTGDR (1.00) PTGDRTBXA2RPTGER2PTGER3PTGIR
Laropiprant SCHEMBL29612617 1.00 PTGDR (1.00) PTGDRTBXA2RPTGER2PTGER3PTGIR
Diastereomer 2 SCHEMBL32668949 1.00 PTGDR (1.00) PTGDRTBXA2RPTGER2PTGER3PTGIR
SCHEMBL991121 0.95 PTGDR (1.00) PTGDRTBXA2RPTGER2PTGER3PTGIR
SCHEMBL4548354 0.95 PTGDR (1.00) PTGDRTBXA2RPTGER2PTGER3PTGIR
SCHEMBL13344157 0.93 PTGDR (0.86) PTGDRTBXA2RPTGER2PTGER3PTGIR
SCHEMBL19799336 0.93 PTGDR (0.86) PTGDRTBXA2RPTGER2PTGER3PTGIR
SCHEMBL13344139 0.93 PTGDR (0.86) PTGDRTBXA2RPTGER2PTGER3PTGIR
Laropiprant SCHEMBL29398067 0.89 PTGDR (0.80) PTGDRTBXA2RPTGER2PTGER3PTGIR
SCHEMBL19861546 0.89 PTGDR (0.80) PTGDRTBXA2RPTGER2PTGER3PTGIR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2295409-B1 FLUORO SUBSTITUTED CYCLOALKANOINDOLES AND THEIR USE AS PROSTAGLANDIN D2 RECEPTOR ANTAGONISTS MERCK CANADA INC (CA) 2014-07-02 EP claimed
EP-2295409-A1 Fluoro substituted cycloalkanoindoles and their use as prostaglandin D2 receptor antagonists Merck Frosst Canada Limited (CA) 2011-03-16 EP claimed
EP-1470107-B1 FLUORO SUBSTITUTED CYCLOALKANOINDOLES AND THEIR USE AS PROSTAGLANDIN D2 RECEPTOR ANTAGONISTS MERCK FROSST CANADA LTD (CA) 2008-11-19 EP claimed
US-20080033028-A1 Fluoro substituted cycloalkanoindoles, compositions containing such compounds and methods of treatment BERTHELETTE CARL 2008-02-07 US claimed
US-20060069148-A1 Fluoro substituted cycloalkanoindoles, compositions containing such compounds and methods of treatment BERTHELETTE CARL 2006-03-30 US claimed
US-20050124680-A1 Fluoro substituted cycloalkanoindoles, compositions containing such compounds and methods of treatment MERCK CANADA INC. (CA) 2005-06-09 US claimed
EP-1470107-A2 FLUORO SUBSTITUTED CYCLOALKANOINDOLES AND THEIR USE AS PROSTAGLANDIN D2 RECEPTOR ANTAGONISTS Merck Frosst Canada & Co. (CA) 2004-10-27 EP claimed
US-20030158246-A1 For the treatment of prostaglandin mediated diseases, such as allergic asthma or rhinitis. MERCK FROSST CANADA & CO. (CA) 2003-08-21 US claimed
WO-2003062200-A2 FLUORO SUBSTITUTED CYCLOALKANOINDOLES AND THEIR USE AS PROSTAGLANDIN D2 RECEPTOR ANTAGONISTS MERCK FROSST CANADA & CO. (CA) 2003-07-31 WO 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-4420734-A2 PTGDR-1 AND/OR PTGDR-2 ANTAGONISTS FOR PREVENTING AND/OR TREATING SYSTEMIC LUPUS ERYTHEMATOSUS Institut National de la Santé et de la Recherche Médicale (FR) 2024-08-28 EP disclosed
EP-3256121-B1 PTGDR-1 AND/OR PTGDR-2 ANTAGONISTS FOR PREVENTING AND/OR TREATING SYSTEMIC LUPUS ERYTHEMATOSUS INST NAT SANTE RECH MED (FR) 2024-08-07 EP disclosed
US-20230330062-A1 PTGDR-1 AND/OR PTGDR-2 ANTAGONISTS FOR PREVENTING AND/OR TREATING SYSTEMIC LUPUS ERYTHEMATOSUS INST NAT SANTE RECH MED (FR) 2023-10-19 US disclosed
US-20070299101-A1 Niacin Receptor Agonists, Compositions Containing Such Compounds and Methods of Treatment MERCK SHARP & DOHME CORP. 2007-12-27 US disclosed
US-20070244107-A1 Method of Treating Atherosclerosis, Dyslipidemias and Related Conditions MERCK & CO., INC. 2007-10-18 US disclosed
US-20060069148-A1 Fluoro substituted cycloalkanoindoles, compositions containing such compounds and methods of treatment BERTHELETTE CARL 2006-03-30 US disclosed
US-20050124680-A1 Fluoro substituted cycloalkanoindoles, compositions containing such compounds and methods of treatment MERCK CANADA INC. (CA) 2005-06-09 US disclosed
US-20040229844-A1 Method of treating atherosclerosis, dyslipidemias and related conditions CHENG KANG (US) 2004-11-18 US disclosed
US-20030158246-A1 For the treatment of prostaglandin mediated diseases, such as allergic asthma or rhinitis. MERCK FROSST CANADA & CO. (CA) 2003-08-21 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 (10 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 16/4885PTGER2 8/4885
US-20060069148-A1 Fluoro substituted cycloalkanoindoles, compositions containing such compounds and methods of treatment PTGER1, PTGER3, PTGER2 PTGDR 7/4885TBXA2R 17/4885PTGER2 3/4885
US-20030158246-A1 For the treatment of prostaglandin mediated diseases, such as allergic asthma or rhinitis. PTGES, PTGIR, PTGER1 PTGDR 14/4885TBXA2R 25/4885PTGER2 5/4885
US-20050124680-A1 Fluoro substituted cycloalkanoindoles, compositions containing such compounds and methods of treatment PTGER1, PTGER3, PTGER2 PTGDR 7/4885TBXA2R 17/4885PTGER2 3/4885
US-20080033028-A1 Fluoro substituted cycloalkanoindoles, compositions containing such compounds and methods of treatment PTGER1, PTGER3, PTGER2 PTGDR 7/4885TBXA2R 17/4885PTGER2 3/4885
US-12589089-B2 PTGDR-1 and/or PTGDR-2 antagonists for preventing and/or treating systemic lupus erythematosus PTGIR, PTGDR, SSB PTGDR 2/4885TBXA2R 13/4885PTGER2 14/4885
US-20070299101-A1 Niacin Receptor Agonists, Compositions Containing Such Compounds and Methods of Treatment LDLR, APOB, FFAR1 PTGDR 591/4885TBXA2R 44/4885PTGER2 466/4885
US-20230330062-A1 PTGDR-1 AND/OR PTGDR-2 ANTAGONISTS FOR PREVENTING AND/OR TREATING SYSTEMIC LUPUS ERYTHEMATOSUS PTGDR2, PTGDR, PTGIR PTGDR 2/4885TBXA2R 10/4885PTGER2 9/4885
US-20070244107-A1 Method of Treating Atherosclerosis, Dyslipidemias and Related Conditions LDLR, LIPA, APOB PTGDR 97/4885TBXA2R 68/4885PTGER2 223/4885
US-20040229844-A1 Method of treating atherosclerosis, dyslipidemias and related conditions LDLR, HCAR1, FFAR1 PTGDR 201/4885TBXA2R 37/4885PTGER2 442/4885

“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.