SCHEMBL2408403

SCHEMBL2408403

CC(C)(C)NS(=O)(=O)c1ccc(N)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.59
MAPT P10636 3/20 0.59
SMN1; SMN2 Q16637 3/20 0.59
CA1 P00915 5/20 0.56
CA2 P00918 5/20 0.56
CA9 Q16790 5/20 0.56
CA12 O43570 4/20 0.56
MMP1 P03956 1/20 0.55
MMP2 P08253 1/20 0.55
MMP9 P14780 1/20 0.55
MMP8 P22894 1/20 0.55
MMP13 P45452 1/20 0.55
CYP3A4 P08684 2/20 0.54
MEN1 O00255 2/20 0.54
KMT2A Q03164 2/20 0.54
CYP1A2 P05177 1/20 0.54
CYP2C19 P33261 1/20 0.54
CYP2C9 P11712 1/20 0.54
MAPK1 P28482 1/20 0.54
DHFR P00374 1/20 0.53

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
SCHEMBL634085 0.81 ALDH1A1 (0.79) ALDH1A1MAPTSMN1; SMN2CA1CA2
SCHEMBL23345377 0.81 ALDH1A1 (0.67) ALDH1A1MAPTSMN1; SMN2CA1CA2
SCHEMBL15840367 0.81 ALDH1A1 (0.67) ALDH1A1MAPTSMN1; SMN2CA1CA2
SCHEMBL6952974 0.80 ALDH1A1 (0.66) ALDH1A1MAPTSMN1; SMN2CA1CA2
SCHEMBL10258693 0.80 ALDH1A1 (0.56) ALDH1A1MAPTSMN1; SMN2CA1CA2
SCHEMBL1479992 0.79 ALDH1A1 (0.59) ALDH1A1MAPTSMN1; SMN2CA1CA2
SCHEMBL2333640 0.79 ALDH1A1 (0.59) ALDH1A1MAPTSMN1; SMN2CA1CA2
SCHEMBL4781214 0.79 CA1 (0.61) ALDH1A1MAPTSMN1; SMN2CA1CA2
SCHEMBL12169369 0.79 ALDH1A1 (0.68) ALDH1A1MAPTSMN1; SMN2CA1CA2
SCHEMBL3834643 0.79 ALDH1A1 (0.80) ALDH1A1MAPTSMN1; SMN2CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8476456-B2 Process for the preparation of 4-(imidazol-1-yl)benzenesulfonamide derivatives PALAU PHARMA, S.A. (ES) 2013-07-02 US claimed
US-20090012307-A1 Process for the Preparation of 4-(imidazol-1-yl)benzenesulfonamide Derivatives PALAU PHARMA, S.A. (ES) 2009-01-08 US claimed
EP-1424329-B1 PROCESS FOR THE PREPARATION OF 4-(IMIDAZOL-1-YL)BENZENESULFONAMIDE DERIVATIVES PALAU PHARMA SA (ES) 2008-05-28 EP claimed
US-20040242872-A1 Method of preparing 4-(imidazole-1-yl)benzenesulphonamide derivatives PALAU PHARMA, S.A. (ES) 2004-12-02 US claimed
EP-1424329-A1 METHOD OF PREPARING 4-(IMIDAZOLE-1-IL)BENZENESULPHONAMIDE DERIVATIVES J. Uriach & Cia. S.A. (ES) 2004-06-02 EP claimed
EP-4719413-A1 INHIBITORS OF CANINE JANUS KINASE AND USES THEREOF Animol Discovery, Inc. (US) 2026-04-08 EP disclosed
US-20260092070-A1 INHIBITORS OF CANINE JANUS KINASE AND USES THEREOF ANIMOL DISCOVERY INC (US) 2026-04-02 US disclosed
US-20250162989-A1 USP30 INHIBITORS AND USES THEREOF VINCERE BIOSCIENCES, INC. 2025-05-22 US disclosed
WO-2024246837-A1 INHIBITORS OF CANINE JANUS KINASE AND USES THEREOF ANIMOL DISCOVERY, INC. (US) 2024-12-05 WO disclosed
US-20240262792-A1 USP30 INHIBITORS AND USES THEREOF VINCERE BIOSCIENCES, INC. 2024-08-08 US disclosed
CN-117836270-A USP30 inhibitors and uses thereof 文森雷生物科学股份有限公司 2024-04-05 CN disclosed
EP-4305021-A1 USP30 INHIBITORS AND USES THEREOF Vincere Biosciences, Inc. (US) 2024-01-17 EP disclosed
US-6638921-B1 Pharmaceutically acceptable derivatives thereof Cx, R1 and R2 being as defined in the disclosure may be used to inhibit the activity of HIV integrase. PHARMACOR INC. (CA) 2003-10-28 US disclosed
WO-2003082881-A2 PYRIDOXAL-5-PHOSPHATE DERIVATIVES AS HIV INTEGRASE INHIBITORS PROCYON BIOPHARMA INC. (CA) 2003-10-09 WO disclosed
WO-2003037887-A1 THERAPEUTIC ISOQUINOLINE COMPOUNDS ASTRAZENECA AB (SE) 2003-05-08 WO disclosed
US-6548512-B1 Pyrazole derivatives such as 1-(3-amidinophenyl)-3-methyl-2-((5-(2'-aminosulfonylphenyl-1-yl)pyrimidin-2 -yl)aminocarbonyl)pyrazole; treating thromboembolic disorders BRISTOL-MYERS SQUIBB PHARMA COMPANY 2003-04-15 US disclosed
CN-1246847-A Nitrogen containing heteroaromatics as factor Xa inhibitors DU PONT MERCK PHARMA (US) 2000-03-08 CN disclosed
US-6020357-A CARDIOVASCULAR DISORDERS; ANTCOAGULANTS DUPONT PHARMACEUTICALS COMPANY (US) 2000-02-01 US disclosed
EP-0946508-A1 NITROGEN CONTAINING HETEROAROMATICS AS FACTOR Xa INHIBITORS Du Pont Pharmaceuticals Company (US) 1999-10-06 EP disclosed
WO-1998028269-A1 NITROGEN CONTAINING HETEROAROMATICS AS FACTOR Xa INHIBITORS DU PONT PHARMACEUTICALS COMPANY (US) 1998-07-02 WO 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 (5 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-20090012307-A1 Process for the Preparation of 4-(imidazol-1-yl)benzenesulfonamide Derivatives IL1B, IL1A, TBXAS1 ALDH1A1 373/4885MAPT 4025/4885SMN1; SMN2 2591/4885
US-20040242872-A1 Method of preparing 4-(imidazole-1-yl)benzenesulphonamide derivatives IL1B, IL1A, IRAK1 ALDH1A1 251/4885MAPT 4155/4885SMN1; SMN2 3307/4885
US-20260092070-A1 INHIBITORS OF CANINE JANUS KINASE AND USES THEREOF JAK1, JAK3, JAK2 ALDH1A1 1691/4885MAPT 3322/4885SMN1; SMN2 4009/4885
US-20250162989-A1 USP30 INHIBITORS AND USES THEREOF USP30, USP28, USP1 ALDH1A1 2021/4885MAPT 2434/4885SMN1; SMN2 1580/4885
US-20240262792-A1 USP30 INHIBITORS AND USES THEREOF USP30, USP28, USP1 ALDH1A1 2021/4885MAPT 2434/4885SMN1; SMN2 1580/4885

“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.