Sulfanilamide

Sulfanilamide

SCHEMBL2215151

CCCC.Nc1ccc(S(N)(=O)=O)cc1

nearest known ligand 0.77

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

folP

The experimentally established mechanism targets of Sulfanilamide. 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
CA2 P00918 17/20 0.77
CA9 Q16790 12/20 0.77
CA1 P00915 12/20 0.77
CA12 O43570 11/20 0.77
CA7 P43166 8/20 0.77
CA14 Q9ULX7 3/20 0.77
CA6 P23280 3/20 0.77
CA5A P35218 3/20 0.77
CA5B Q9Y2D0 3/20 0.77
TSHR P16473 2/20 0.77
CA13 Q8N1Q1 2/20 0.77
CA4 P22748 2/20 0.77
USP2 O75604 1/20 0.77
TDP1 Q9NUW8 1/20 0.77
AGO2 Q9UKV8 1/20 0.77
GAA P10253 1/20 0.59
SMN1; SMN2 Q16637 1/20 0.57
HTT P42858 1/20 0.55
CA3 P07451 1/20 0.54

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
Sulfanilamide SCHEMBL27635251 0.90 CA2 (0.68) CA2CA9CA1CA12CA7
Sulfanilamide SCHEMBL419065 0.89 CA2 (0.74) CA2CA9CA1CA12CA7
Sulfanilamide SCHEMBL4188099 0.88 CA2 (0.90) CA2CA9CA1CA12CA7
Sulfanilamide SCHEMBL2798899 0.88 CA2 (1.00) CA2CA9CA1CA12CA7
Sulfanilamide SCHEMBL740 0.88 CA2 (1.00) CA2CA9CA1CA12CA7
Sulfanilamide SCHEMBL31544839 0.88 CA2 (1.00) CA2CA9CA1CA12CA7
Sulfanilamide SCHEMBL30659052 0.88 CA2 (1.00) CA2CA9CA1CA12CA7
Sulfanilamide SCHEMBL737140 0.87 CA2 (0.71) CA2CA9CA1CA12CA7
Sulfanilamide SCHEMBL28201481 0.86 CA2 (0.85) CA2CA9CA1CA12CA7
Sulfanilamide SCHEMBL27364276 0.86 CA2 (0.85) CA2CA9CA1CA12CA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11950480-B2 Color correction filter for white organic electroluminescent light source, and organic electroluminescent display device FUJIFILM CORPORATION (JP) 2024-04-02 US disclosed
US-20210005673-A1 COLOR CORRECTION FILTER FOR WHITE ORGANIC ELECTROLUMINESCENT LIGHT SOURCE, AND ORGANIC ELECTROLUMINESCENT DISPLAY DEVICE FUJIFILM CORPORATION (JP) 2021-01-07 US disclosed
CN-107995910-A The inhibitor of human immunodeficiency virus replication VIIV保健英国第五有限公司 2018-05-04 CN disclosed
EP-1745032-B1 CXCR1 and CXCR2 chemokine antagonists MERCK SHARP & DOHME (US) 2013-07-31 EP disclosed
CN-101605728-B Systems and methods for removing fluorine-containing compounds from water 3M INNOVATIVE PROPERTIES CO 2013-07-24 CN disclosed
EP-2361246-A1 OXOPIPERIDINYL AND PYRANYL SULFONAMIDES AS AMPA POTENTIATORS Pfizer Inc. (US) 2011-08-31 EP disclosed
US-20110172297-A1 Oxopiperdinyl And Pyranyl Sulfonamides and Pharmaceutical Compositions Thereof PFIZER INC 2011-07-14 US disclosed
WO-2010038167-A1 OXOPIPERIDINYL AND PYRANYL SULFONAMIDES AS AMPA POTENTIATORS PFIZER INC. (US) 2010-04-08 WO disclosed
CN-101605728-A Systems and methods for removing fluorine-containing compounds from water 3M INNOVATIVE PROPERTIES CO (US) 2009-12-16 CN disclosed
US-7326729-B2 CXCR1 and CXCR2 chemokine antagonists SCHERING CORPORATION (US) 2008-02-05 US disclosed
EP-0821670-A1 N-AROYLAMINO ACID AMIDES AS ENDOTHELIN INHIBITORS Novartis AG (CH) 1998-02-04 EP disclosed
WO-1996033170-A1 N-AROYLAMINO ACID AMIDES AS ENDOTHELIN INHIBITORS NOVARITS AG (CH) 1996-10-24 WO disclosed
EP-0351603-B1 Transvinylation reaction UNION CARBIDE CORP (US) 1994-12-07 EP disclosed
US-5155253-A Reacting vinyl derivative of first Bronsted acid with labile Bronsted acid in presence of ruthenium catalyst, maintaining concentration below certain level and removing product as formed UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1992-10-13 US disclosed
EP-0506070-A2 Transvinylation process for the preparation of thermally labile vinyl compounds and vinyl compounds prepared from thermally labile acids UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1992-09-30 EP disclosed
US-4981973-A BRONSTED ACID, RUTHENIUM CATALYST UNION CARBIDE CHEMICALS AND PLASTICS COMPANY, INC. (US) 1991-01-01 US disclosed
EP-0351603-A2 Transvinylation reaction UNION CARBIDE CORPORATION (US) 1990-01-24 EP disclosed
CN-86102681-A The preparation method of p-aminophenol derivative and purposes 1987-10-28 CN disclosed
US-4220630-A ORGANIC SULFONIC ACID DEFOAMER OCCIDENTAL PETROLEUM CORPORATION (US) 1980-09-02 US disclosed
US-4196172-A FROM PHOSPHATE ROCK AND SULFURIC ACID OCCIDENTAL PETROLEUM CORPORATION (US) 1980-04-01 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-20110172297-A1 Oxopiperdinyl And Pyranyl Sulfonamides and Pharmaceutical Compositions Thereof GRIK5, GABRE, GRIK2 CA2 1400/4885CA9 4017/4885CA1 1941/4885

“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.