SCHEMBL6097355

SCHEMBL6097355

Cc1ccc(S(=O)(=O)O)cc1.Cc1nn(-c2ccc(CCNC(=O)NS(=O)(=O)c3ccc(C(C)(C)C)cc3)cc2)c(C)c1-c1ccccc1

nearest known ligand 0.49

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
PTGER4 P35408 8/20 0.49
CA1 P00915 6/20 0.47
CA2 P00918 6/20 0.47
CA12 O43570 3/20 0.47
CA9 Q16790 3/20 0.47
MAPK13 O15264 1/20 0.42
MAPK12 P53778 1/20 0.42
MAPK11 Q15759 1/20 0.42
MAPK14 Q16539 1/20 0.42
CA4 P22748 3/20 0.41
CA7 P43166 3/20 0.41
TBXA2R P21731 1/20 0.41
PTGER3 P43115 1/20 0.41
PTGER2 P43116 1/20 0.41
POLB P06746 1/20 0.41
MAPT P10636 1/20 0.41
RAB9A P51151 2/20 0.41
NPC1 O15118 1/20 0.41
FPR1 P21462 1/20 0.40

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
SCHEMBL6098510 0.94 CA1 (0.48) PTGER4CA1CA2CA12CA9
SCHEMBL6096713 0.94 CA1 (0.52) PTGER4CA1CA2CA12CA9
SCHEMBL6096770 0.93 CA1 (0.47) PTGER4CA1CA2CA12CA9
SCHEMBL6095181 0.91 CA1 (0.49) PTGER4CA1CA2CA12CA9
SCHEMBL6097730 0.91 PTGER4 (0.53) PTGER4CA1CA2CA12CA9
SCHEMBL4446913 0.91 CA1 (0.56) PTGER4CA1CA2CA12CA9
SCHEMBL6097860 0.90 CA12 (0.55) PTGER4CA1CA2CA12CA9
SCHEMBL6096359 0.89 CA1 (0.53) PTGER4CA1CA2CA12CA9
SCHEMBL6097743 0.89 CA1 (0.47) PTGER4CA1CA2CA12CA9
SCHEMBL6098095 0.88 PTGER4 (0.45) PTGER4CA1CA2CA12CA9

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 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7001917-B2 Pyrazole compounds as anti-inflammatory and analgesic agents WARNER LAMBERT COMPANY LLC (US) 2006-02-21 US disclosed
US-20040019045-A1 2-(4-(4-(4-Fluorophenyl)-3,5-imethyl-1H-pyrazol-1-yl)phenyl) ethyl (4-methylphenyl)sulfonylcarbamate ammonium salt, e.g., as an antagonist for Prostoglandin E receptor; analgesics; antipyretics; antiinflammatory agents HIRANO MISATO (JP) 2004-01-29 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 (1 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-20040019045-A1 2-(4-(4-(4-Fluorophenyl)-3,5-imethyl-1H-pyrazol-1-yl)phenyl) ethyl (4-methylphenyl)sulfonylcarbamate ammonium salt, e.g., as an antagonist for Prostoglandin E receptor; analgesics; antipyretics; antiinflammatory agents PTGER1, PTGS1, PTGIR PTGER4 5/4885CA1 1837/4885CA2 230/4885

“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.