SCHEMBL696313

SCHEMBL696313

Cc1ccc[c]c1S(=O)(=O)O

nearest known ligand 0.33

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
MYC P01106 1/20 0.32
CA1 P00915 2/20 0.31
CA2 P00918 2/20 0.31
CA7 P43166 2/20 0.31
CA9 Q16790 2/20 0.31
ALDH1A1 P00352 1/20 0.31
ACHE P22303 1/20 0.31
SUMO2 P61956 1/20 0.30
SUMO1 P63165 1/20 0.30
SENP7 Q9BQF6 1/20 0.30
SENP3 Q9H4L4 1/20 0.30
SENP2 Q9HC62 1/20 0.30
SENP1 Q9P0U3 1/20 0.30

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
SCHEMBL11798388 0.82 KDM4E (0.40) MYCALDH1A1
SCHEMBL15415279 0.81 KEAP1 (0.34) TSHRCA1CA2CA7CA9
SCHEMBL11077665 0.79 HTR6 (0.37) TSHRSMN1; SMN2ALDH1A1ACHE
SCHEMBL11798381 0.77 HSD11B1 (0.39) MYCALDH1A1SUMO2SUMO1SENP7
SCHEMBL691617 0.77 ALDH1A1 (0.35) TSHRSMN1; SMN2ALDH1A1
SCHEMBL483018 0.77 SMN1; SMN2 (0.34) TSHRSMN1; SMN2CA2ALDH1A1
SCHEMBL692167 0.77 TTR (0.38) TSHRSMN1; SMN2MYC
SCHEMBL5152547 0.76 GABRA1 (0.39) TSHRSMN1; SMN2ALDH1A1
SCHEMBL15303121 0.75 TDP2 (0.30)
SCHEMBL458583 0.75 TTR (0.41) TSHRSMN1; SMN2CA1CA2CA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1633733-A4 CANNABINOID DERIVATIVES, METHODS OF MAKING, AND USE THEREOF UNIV TENNESSEE RES CORP (US) 2007-02-28 EP claimed
US-7169942-B2 agonists or antagonists; treatment for neuroinflammatory pathologies involving demyelinization, viral encephalitis, cerebrovascular accidents, cranial trauma, ocular disorders, pulmonary disorders, allergic diseases, inflammatory conditions, immune system disorders, central nervous system diseases, etc. UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2007-01-30 US claimed
JP-2007501279-A 2007-01-25 JP claimed
EP-1633733-A1 CANNABINOID DERIVATIVES, METHODS OF MAKING, AND USE THEREOF THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2006-03-15 EP claimed
US-20050026077-A1 Forming relief images; for ((opto)electronics; photoresists; mixture of binder and photoactivable compound SHIPLEY COMPANY, L.L.C. (US) 2005-02-03 US claimed
WO-2004113320-A1 CANNABINOID DERIVATIVES, METHODS OF MAKING, AND USE THEREOF THE UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION (US) 2004-12-29 WO claimed
US-20040242593-A1 Cannabinoid derivatives, methods of making, and use thereof UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION 2004-12-02 US claimed
EP-1407324-A1 PHOTOIMAGEABLE COMPOSITION Shipley Company LLC (US) 2004-04-14 EP claimed
US-20030099899-A1 Photoimageable composition SHIPLEY COMPANY, L.L.C. 2003-05-29 US claimed
WO-2002091083-A1 PHOTOIMAGEABLE COMPOSITION SHIPLEY COMPANY, L.L.C. (US) 2002-11-14 WO claimed
EP-0778284-A2 New 7-beta-substituted-4-aza-5alpha-androstan-3-ones as 5alpha-reductase inhibitors MERCK & CO. INC. (US) 1997-06-11 EP claimed
EP-0572166-A1 New 7beta-substituted-4-aza-5a-androstan-3-ones as 5a-reductase inhibitors MERCK & CO. INC. (US) 1993-12-01 EP claimed
WO-1993023039-A1 SUBSTITUTED 4-AZA-5A-ANDROSTAN-ONES AS 5A-REDUCTASE INHIBITORS MERCK & CO., INC. (US) 1993-11-25 WO claimed
WO-1993023420-A1 NEW 7β-SUBSTITUTED-4-AZA-5α-ANDROSTAN-3-ONES AS 5α-REDUCTASE INHIBITORS MERCK & CO., INC. (US) 1993-11-25 WO claimed
US-5151430-A Specific 17β-thiobenzoyl-4-aza-5α-androst-1-en-3-ones as antiandrogen agents MERCK & CO., INC. (US) 1992-09-29 US claimed
EP-0071985-B1 WATER-SOLUBLE MONO-AZO COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THEIR USE AS DYESTUFFS HOECHST AKTIENGESELLSCHAFT (DE) 1985-03-20 EP claimed
EP-0071985-A2 Water-soluble mono-azo compounds, process for their preparation and their use as dyestuffs HOECHST AKTIENGESELLSCHAFT (DE) 1983-02-16 EP claimed
EP-2421613-A2 KERATIN DYEING COMPOSITIONS COMPRISING A RADICAL SCAVENGER AND A CHELANT AND USE THEREOF The Procter & Gamble Company (US) 2012-02-29 EP disclosed
EP-0071985-B1 WATER-SOLUBLE MONO-AZO COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THEIR USE AS DYESTUFFS HOECHST AKTIENGESELLSCHAFT (DE) 1985-03-20 EP disclosed
EP-0071985-A2 Water-soluble mono-azo compounds, process for their preparation and their use as dyestuffs HOECHST AKTIENGESELLSCHAFT (DE) 1983-02-16 EP 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-20040242593-A1 Cannabinoid derivatives, methods of making, and use thereof CNR2, CNR1, GPR18 TSHR 1808/4885SMN1; SMN2 2941/4885MYC 3300/4885

“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.