SCHEMBL120702

SCHEMBL120702

COc1ccc(S(=O)(=O)NCc2ccccc2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 8/20 1.00
CYP19A1 P11511 1/20 0.80
POLB P06746 2/20 0.73
TSHR P16473 2/20 0.72
HTT P42858 2/20 0.71
KEAP1 Q14145 1/20 0.69
CA12 O43570 1/20 0.69
CYP1A2 P05177 1/20 0.69
CYP3A4 P08684 1/20 0.69
ATM Q13315 1/20 0.69
CA9 Q16790 1/20 0.69
L3MBTL1 Q9Y468 1/20 0.69
SMN1; SMN2 Q16637 2/20 0.68
LMNA P02545 1/20 0.68
PKM P14618 2/20 0.62
USP2 O75604 1/20 0.61
TDP1 Q9NUW8 1/20 0.61

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
SCHEMBL3659182 0.94 ALDH1A1 (0.88) ALDH1A1CYP19A1POLBTSHRHTT
SCHEMBL12793674 0.86 ALDH1A1 (0.78) ALDH1A1CYP19A1POLBTSHRHTT
SCHEMBL19636581 0.86 ALDH1A1 (1.00) ALDH1A1CYP19A1TSHRHTTCA12
SCHEMBL13310570 0.86 ALDH1A1 (0.78) ALDH1A1CYP19A1POLBTSHRHTT
SCHEMBL22234016 0.85 ALDH1A1 (0.74) ALDH1A1CYP19A1POLBTSHRHTT
SCHEMBL6272107 0.84 ALDH1A1 (0.76) ALDH1A1CYP19A1TSHRHTTSMN1; SMN2
SCHEMBL7109149 0.84 ALDH1A1 (1.00) ALDH1A1POLBSMN1; SMN2PKM
SCHEMBL3914871 0.84 ALDH1A1 (0.76) ALDH1A1CYP19A1TSHRHTTL3MBTL1
SCHEMBL1893565 0.84 ALDH1A1 (0.76) ALDH1A1CYP19A1TSHRHTTCA9
SCHEMBL13419650 0.84 ALDH1A1 (0.76) ALDH1A1CYP19A1TSHRHTTSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117964526-A Synthesis and application of (4-benzyl (p-toluenesulfonyl) amino) benzenesulfonamide compound 赣南医学院 2024-05-03 CN disclosed
CN-112047865-B Method for synthesizing N-alkyl sulfonamide in water 南京理工大学 2022-12-02 CN disclosed
CN-106279044-B Pyrimidine hydroxamic acid derivative and preparation method and application thereof 厦门市博瑞来医药科技有限公司 2021-02-19 CN disclosed
CN-112047865-A Method for synthesizing N-alkyl sulfonamide in water 南京理工大学 2020-12-08 CN disclosed
CN-104418678-B A kind of method of synthetic N-alkyl sulfonamide derivatives NANJING UNIVERSITY OF SCIENCE AND TECHNOLOGY (CN) 2016-05-18 CN disclosed
CN-104418678-A Method for synthesizing N-alkyl sulfonamide derivative UNIV NANJING SCIENCE & TECH 2015-03-18 CN disclosed
US-20120094964-A1 SULFAMOYL BENZOIC ACID DERIVATIVES AS TRPM8 ANTAGONISTS RAQUALIA PHARMA INC. (JP) 2012-04-19 US disclosed
EP-2424517-A1 SULFAMOYL BENZOIC ACID DERIVATIVES AS TRPM8 ANTAGONISTS RaQualia Pharma Inc (JP) 2012-03-07 EP disclosed
WO-2010125831-A1 SULFAMOYL BENZOIC ACID DERIVATIVES AS TRPM8 ANTAGONISTS RAQUALIA PHARMA INC. (JP) 2010-11-04 WO disclosed
US-7348017-B2 Dithiazole compounds, matrix metalloprotease inhibitors and external preparations for the skin SHISEIDO CO., LTD. (JP) 2008-03-25 US disclosed
WO-1998016503-A2 THE PREPARATION AND USE OF ORTHO-SULFONAMIDO ARYL HYDROXAMIC ACIDS AS MATRIX METALLOPROTEINASE AND TACE INHIBITORS AMERICAN CYANAMID COMPANY (US) 1998-04-23 WO disclosed
WO-1998016514-A1 ORTHO-SULFONAMIDO BICYCLIC HETEROARYL HYDROXAMIC ACIDS AS MATRIX METALLOPROTEINASE AND TACE INHIBITORS AMERICAN CYANAMID COMPANY (US) 1998-04-23 WO disclosed
EP-0801083-A2 Improved functionalized resin for chemical synthesis PFIZER INC. (US) 1997-10-15 EP disclosed
EP-0606046-B1 Arylsulfonamido-substituted hydroxamic acids CIBA GEIGY AG (CH) 1997-10-08 EP disclosed
US-5672615-A MATRIX-DEGRADING METALLOPROTEINASE INHIBITORS NOVARTIS CORPORATION (US) 1997-09-30 US disclosed
US-5646167-A ADMINISTERED AS METALLOPROTEINASE INHIBITOR, ANTITUMOR OR ANTICARCINOGENIC AGENT CIBA-GEIGY CORPORATION (US) 1997-07-08 US disclosed
US-5552419-A METALLOPROTEINASE INHIBITORS CIBA-GEIGY CORPORATION (US) 1996-09-03 US disclosed
US-5506242-A METALLOELASTASE INHIBITOR; TREATS EMPHYSEMA CIBA-GEIGY CORPORATION (US) 1996-04-09 US disclosed
US-5455258-A Useful as inhibitors of matrix-degrading metalloproteinase enzymes such as stromelysin and/or collegenase CIBA-GEIGY CORPORATION (US) 1995-10-03 US disclosed
EP-0606046-A1 Arylsulfonamido-substituted hydroxamic acids CIBA-GEIGY AG (CH) 1994-07-13 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-20120094964-A1 SULFAMOYL BENZOIC ACID DERIVATIVES AS TRPM8 ANTAGONISTS TRPM8, TRPM5, TRPM6 ALDH1A1 1996/4885CYP19A1 3568/4885POLB 4630/4885

“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.