SCHEMBL8575008

SCHEMBL8575008

CC(C)NS(=O)(=O)c1ccc([N+](=O)[O-])cc1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 7/20 0.65
CA12 O43570 5/20 0.65
CA9 Q16790 5/20 0.65
CA1 P00915 5/20 0.65
CA14 Q9ULX7 4/20 0.65
CA3 P07451 2/20 0.65
CA4 P22748 2/20 0.65
CA6 P23280 2/20 0.65
CA5A P35218 2/20 0.65
CA7 P43166 2/20 0.65
CA13 Q8N1Q1 2/20 0.65
CA5B Q9Y2D0 2/20 0.65
MMP2 P08253 4/20 0.61
MMP9 P14780 3/20 0.60
MMP1 P03956 2/20 0.60
MMP13 P45452 2/20 0.60
MMP3 P08254 1/20 0.60
MMP7 P09237 1/20 0.60
MMP8 P22894 1/20 0.59
SLC1A3 P43003 1/20 0.55

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
SCHEMBL2492568 0.95 MMP2 (0.68) CA2CA12CA9CA1CA14
SCHEMBL31219603 0.83 MAPT (0.60) CA2CA12CA9CA1CA14
SCHEMBL23788364 0.82 CA2 (0.57) CA2CA12CA9CA1CA14
SCHEMBL5193258 0.82 MMP2 (0.68) CA2CA12CA9CA1CA14
SCHEMBL17526270 0.82 CA2 (0.66) CA2CA12CA9CA1CA5A
SCHEMBL22492652 0.82 MMP2 (0.68) CA2CA12CA9CA1CA14
SCHEMBL7000224 0.81 CA2 (0.51) CA2CA12CA9CA1CA14
SCHEMBL4950672 0.80 ALDH1A1 (0.62) CA2CA12CA9CA1CA14
SCHEMBL4950680 0.80 ALDH1A1 (0.62) CA2CA12CA9CA1CA14
SCHEMBL6422533 0.79 MMP2 (0.92) MMP2MMP9MMP1MMP13MMP3

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 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
WO-2024246837-A1 INHIBITORS OF CANINE JANUS KINASE AND USES THEREOF ANIMOL DISCOVERY, INC. (US) 2024-12-05 WO disclosed
US-8809369-B2 Tetrahydroquinoline derivatives HOFFMANN-LA ROCHE INC. (US) 2014-08-19 US disclosed
EP-2668165-A1 NOVEL TETRAHYDROQUINOLINE DERIVATIVES F.HOFFMANN-LA ROCHE AG (CH) 2013-12-04 EP disclosed
CN-103328449-A Novel tetrahydroquinoline derivatives HOFFMANN LA ROCHE 2013-09-25 CN disclosed
WO-2012101068-A1 NOVEL TETRAHYDROQUINOLINE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2012-08-02 WO disclosed
US-20120190677-A1 NOVEL TETRAHYDROQUINOLINE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2012-07-26 US disclosed
US-20070179180-A1 Novel m3 muscarinic acetylcholine receptor antagonists GLAXO GROUP LIMITED (GB) 2007-08-02 US disclosed
US-5783699-A MAY BE CONJUGATED TO ANTIGENS, HAPTENS, ANTIBODIES IN IMMUNOASSAYS ABBOTT LABORATORIES (US) 1998-07-21 US disclosed
US-5669819-A IMMUNOASSAY ABBOTT LABORATORIES (US) 1997-09-23 US disclosed
US-5565570-A REACTING AMINE WITH SULFONYL HALIDE IN INERT SOLVENT IN PRESENCE OF BASE TO FORM METAL SALT OF SULFONAMIDE, ACYLATING WITH ACTIVATED PHENANTHRIDINE-6-CARBOXYLIC ACID TO FORM CHEMILUMINESCENT SALT ABBOTT LABORATORIES (US) 1996-10-15 US disclosed
US-5545739-A E.G., 5-METHYL-6-(N-2-CARBOXYETHYL-N=(2-CARBOXYETHYL)-PHENANTHRIDIN IUMCARBOXAMIDE CHLORIDE; IMMUNOASSAYS; STABILITY; SENSITIVITY ABBOTT LABORATORIES (US) 1996-08-13 US disclosed
US-5543524-A FORMING A SULFONAMIDE FROM AND AMINE AND A SULFONYL HALIDE AND AND ACYLATING WITH A CARBONYL HALIDE OF AN ACTIVATED ACRIDINE SALT ABBOTT LABORATORIES (US) 1996-08-06 US disclosed
US-5468646-A Chemiluminescent acridinium salts ABBOTT LABORATORIES (US) 1995-11-21 US disclosed
EP-0273115-B1 Chemiluminescent acridinium and phenanthridinium salts ABBOTT LAB (US) 1994-09-07 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 (3 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-20070179180-A1 Novel m3 muscarinic acetylcholine receptor antagonists CHRM3, CHRM2, CHRNA3 CA2 1234/4885CA12 1787/4885CA9 3667/4885
US-20120190677-A1 NOVEL TETRAHYDROQUINOLINE DERIVATIVES RAB1A, RABL3, RAB7A CA2 3809/4885CA12 4462/4885CA9 4194/4885
US-20260092070-A1 INHIBITORS OF CANINE JANUS KINASE AND USES THEREOF JAK1, JAK3, JAK2 CA2 1072/4885CA12 4095/4885CA9 3140/4885

“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.