SCHEMBL8071

SCHEMBL8071

O=S(=O)(Cl)c1ccccc1Br

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 3/20 0.62
CA2 P00918 3/20 0.62
CA4 P22748 2/20 0.62
CA6 P23280 2/20 0.62
PLCG1 P19174 1/20 0.58
MAPT P10636 1/20 0.44
TDP1 Q9NUW8 3/20 0.44
ALDH1A1 P00352 1/20 0.44
HSD17B10 Q99714 1/20 0.44
AKR1B1 P15121 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.41
RECQL P46063 1/20 0.41
LOX P28300 1/20 0.41
POLB P06746 3/20 0.40
CA5A P35218 2/20 0.39
CA9 Q16790 2/20 0.39
CA12 O43570 1/20 0.39
CYP2C9 P11712 1/20 0.39
CA7 P43166 1/20 0.39
CA14 Q9ULX7 1/20 0.39

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
SCHEMBL29540971 1.00 CA1 (0.62) CA1CA2CA4CA6PLCG1
Pyridine SCHEMBL6698276 0.86 CA1 (0.48) CA1CA2CA4CA6PLCG1
SCHEMBL6294222 0.82 CA1 (0.48) CA1CA2CA4CA6PLCG1
SCHEMBL841244 0.81 CA2 (0.46) CA1CA2CA4CA6PLCG1
SCHEMBL250199 0.81 ALDH1A1 (0.55) CA1CA2CA4CA6PLCG1
SCHEMBL25294557 0.79 CA2 (0.45) CA1CA2CA4CA6PLCG1
SCHEMBL31152920 0.79 CA2 (0.45) CA1CA2CA4CA6PLCG1
SCHEMBL38660050 0.79 CA1 (0.68) CA1CA2CA4CA6PLCG1
SCHEMBL2475835 0.79 CA1 (0.68) CA1CA2CA4CA6PLCG1
SCHEMBL11521127 0.78 CA2 (0.52) CA1CA2CA4CA6PLCG1

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 1472 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119425423-A Positively charged composite membrane and preparation method and application thereof 中国石油化工股份有限公司 2025-02-14 CN claimed
CN-117603097-B Method for rapidly preparing 2-bromo-5-nitrobenzenesulfonyl chloride 安徽泽升科技股份有限公司 2024-06-18 CN claimed
CN-117924290-A Preparation method and application of long-life organic room-temperature phosphorescent material of filter paper matrix 天津理工大学 2024-04-26 CN claimed
CN-117603097-A Method for rapidly preparing 2-bromo-5-nitrobenzenesulfonyl chloride 安徽泽升科技股份有限公司 2024-02-27 CN claimed
CN-117551005-A Synthesis method of 2-bromobenzenesulfonyl chloride and derivatives thereof 常州锐博生物科技有限公司 2024-02-13 CN claimed
CN-115181100-A Sulfonamide micromolecule inhibitor with purine and pyrrolopyrimidine parent nucleus 广西大学 2022-10-14 CN claimed
CN-111675716-B Fangchinoline derivative with anticancer activity and preparation method and application thereof 山东省农业科学院农产品研究所 2022-09-13 CN claimed
CN-217313437-U Continuous production system of 2-bromobenzene sulfonyl chloride 常州锐博生物科技有限公司 2022-08-30 CN claimed
CN-113185435-A Method for preparing beta-carbonyl sulfone compound by using half-sandwich iridium complex 上海应用技术大学 2021-07-30 CN claimed
CN-108727224-B Process for preparing intermediates for the synthesis of pharmaceuticals 株式会社LG化学 2021-03-23 CN claimed
EP-1328523-A2 METHODS FOR THE PREPARATION OF BIPHENYL ISOXAZOLE SULFONAMIDES Bristol-Myers Squibb Company (US) 2003-07-23 EP claimed
US-20020132838-A1 Methods for the preparation of biphenyl isoxazole sulfonamides BRISTOL-MYERS SQUIBB COMPANY 2002-09-19 US claimed
WO-2002032884-A2 METHODS FOR THE PREPARATION OF BIPHENYL ISOXAZOLE SULFONAMIDES BRISTOL-MYERS SQUIBB COMPANY (US) 2002-04-25 WO claimed
EP-0904077-A4 METHODS FOR THE PREPARATION OF BIPHENYL ISOXAZOLE SULFONAMIDES BRISTOL MYERS SQUIBB CO (US) 1999-12-22 EP claimed
EP-0904077-A2 METHODS FOR THE PREPARATION OF BIPHENYL ISOXAZOLE SULFONAMIDES BRISTOL-MYERS SQUIBB COMPANY (US) 1999-03-31 EP claimed
CN-1211183-A Methods for preparation of biphenyl isoxazole sulfonamides BRISTOL MYERS SQUIBB CO (US) 1999-03-17 CN claimed
EP-0576229-B1 Low temperature process for preparing alpha-anomer enriched 2-deoxy-2, 2-difluoro-D-ribofuranosyl sulfonates LILLY CO ELI (US) 1997-12-17 EP claimed
WO-1997029747-A1 METHODS FOR THE PREPARATION OF BIPHENYL ISOXAZOLE SULFONAMIDES BRISTOL-MYERS SQUIBB COMPANY (US) 1997-08-21 WO claimed
US-5401861-A CONTACTING A LACTOL WITH AN AMINE BASE, COOLING AND ADDING A SULFONATING REAGENT ELI LILLY AND COMPANY (US) 1995-03-28 US claimed
EP-0576229-A1 Low temperature process for preparing alpha-anomer enriched 2-deoxy-2, 2-difluoro-D-ribofuranosyl sulfonates ELI LILLY AND COMPANY (US) 1993-12-29 EP claimed

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-20020132838-A1 Methods for the preparation of biphenyl isoxazole sulfonamides REN, STS, CYP4X1 CA1 2974/4885CA2 602/4885CA4 717/4885

“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.