SCHEMBL104524

SCHEMBL104524

CC(=O)Nc1ccc(C(C)C)cc1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 5/20 0.61
HTT P42858 1/20 0.61
L3MBTL1 Q9Y468 1/20 0.61
KIF11 P52732 1/20 0.61
KMT2A Q03164 6/20 0.59
MEN1 O00255 4/20 0.59
ALDH1A1 P00352 4/20 0.59
CA12 O43570 2/20 0.59
CA1 P00915 2/20 0.59
CA2 P00918 2/20 0.59
CA9 Q16790 2/20 0.59
MAPT P10636 2/20 0.59
TDP1 Q9NUW8 1/20 0.59
BRD4 O60885 1/20 0.59
NR1I2 O75469 1/20 0.59
MB P02144 1/20 0.59
CYP1A1 P04798 1/20 0.59
CA3 P07451 1/20 0.59
CYP3A4 P08684 1/20 0.59
RARG P13631 1/20 0.59

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
SCHEMBL12591828 0.94 SMN1; SMN2 (0.73) SMN1; SMN2HTTL3MBTL1KIF11KMT2A
SCHEMBL14463078 0.85 SMN1; SMN2 (0.59) SMN1; SMN2HTTL3MBTL1KMT2AMEN1
SCHEMBL19707622 0.84 RAB9A (0.76) SMN1; SMN2KIF11KMT2AMEN1CA12
SCHEMBL4579197 0.83 SMN1; SMN2 (0.57) SMN1; SMN2HTTL3MBTL1KIF11KMT2A
SCHEMBL861674 0.83 SMN1; SMN2 (0.84) SMN1; SMN2HTTL3MBTL1KMT2AMEN1
SCHEMBL8643836 0.83 SMN1; SMN2 (0.57) SMN1; SMN2HTTL3MBTL1KIF11KMT2A
SCHEMBL8811830 0.83 SMN1; SMN2 (0.57) SMN1; SMN2HTTL3MBTL1KMT2AMEN1
SCHEMBL18509213 0.83 SMN1; SMN2 (0.57) SMN1; SMN2HTTL3MBTL1KMT2AMEN1
SCHEMBL19806131 0.83 SMN1; SMN2 (0.57) SMN1; SMN2HTTL3MBTL1KMT2AMEN1
SCHEMBL8648800 0.83 SMN1; SMN2 (0.57) SMN1; SMN2HTTL3MBTL1KIF11KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024151833-A1 SPIRO DERIVATIVES AS M4 ACTIVATORS/MODULATORS AND USES THEREOF CEREVEL THERAPEUTICS, LLC (US) 2024-07-18 WO disclosed
WO-2024092083-A1 SMALL MOLECULAR WEIGHT CHEMICAL COMPOUND TO ANTAGONIZE EPH-EPHRIN TETRAMERIZATION AND INHIBIT BIDIRECTIONAL SIGNALING THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2024-05-02 WO disclosed
EP-4360710-A2 1,3-DI-OXO-INDENE DERIVATIVE, PHARMACEUTICALLY ACCEPTABLE SALT OR OPTICAL ISOMER THEREOF, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AS AN ANTIVIRAL, ACTIVE INGREDIENT Korea Research Institute of Chemical Technology (KR) 2024-05-01 EP disclosed
US-11912693-B2 Compounds for modulating S1P1 activity and methods of using the same TREVENA, INC. (US) 2024-02-27 US disclosed
US-11912693-B2 Compounds for modulating S1P1 activity and methods of using the same TREVENA, INC. (US) 2024-02-27 US disclosed
CN-113429356-B Triazole sulfonamide derivative and application thereof in agriculture 东莞市东阳光农药研发有限公司 2024-01-16 CN disclosed
EP-3611158-B1 1,3-DI-OXO-INDENE DERIVATIVE, PHARMACEUTICALLY ACCEPTABLE SALT OR OPTICAL ISOMER THEREOF, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AS AN ANTIVIRAL, ACTIVE INGREDIENT KOREA RES INST CHEMICAL TECH (KR) 2023-12-20 EP disclosed
EP-3746421-B1 ANTAGONISTS OF THE MUSCARINIC ACETYLCHOLINE RECEPTOR M4 UNIV VANDERBILT (US) 2023-11-29 EP disclosed
US-11806335-B2 Heterocyclic carboxylate compounds as glycolate oxidase inhibitors Lilac Therapeutics, Inc. (US) 2023-11-07 US disclosed
US-11806335-B2 Heterocyclic carboxylate compounds as glycolate oxidase inhibitors Lilac Therapeutics, Inc. (US) 2023-11-07 US disclosed
EP-1095931-A1 Benzidine derivatives and electrophotosensitive material using the same KYOCERA MITA CORPORATION (JP) 2001-05-02 EP disclosed
EP-1081138-A1 1,2-disubstituted 1,4-dihydro-4-oxoquinoline compounds Maruishi Pharmaceutical Co., Ltd. (JP) 2001-03-07 EP disclosed
CN-1268116-A 3-amidinoaniline derivatives activated blood coagulation factor X inhibitors, and intermediates for producing both KISSEI PHARMACEUTICAL (JP) 2000-09-27 CN disclosed
EP-0648737-B1 Benzidine derivatives and electrophotosensitive material using the same MITA INDUSTRIAL CO LTD (JP) 1998-07-15 EP disclosed
EP-0799818-A2 Benzidine derivatives and electrophotosensitive material using the same MITA INDUSTRIAL CO. LTD. (JP) 1997-10-08 EP disclosed
US-5550290-A CHARGE TRANSFER COMPOUND MITA INDUSTRIAL CO. LTD. (JP) 1996-08-27 US disclosed
EP-0648737-A1 Benzidine derivatives and electrophotosensitive material using the same MITA INDUSTRIAL CO. LTD. (JP) 1995-04-19 EP disclosed
US-4629495-A Herbicidal 5-amino-4-cyano-1-phenylpyrazoles MAY & BAKER LIMITED (GB) 1986-12-16 US disclosed
EP-0034292-B1 PROCESS FOR THE PREPARATION OF ANTHRANILIC ACID DERIVATIVES F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1983-11-23 EP disclosed
EP-0034292-A2 Process for the preparation of anthranilic acid derivatives F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1981-08-26 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 (2 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-11806335-B2 Heterocyclic carboxylate compounds as glycolate oxidase inhibitors UGDH, PGD, PNPO SMN1; SMN2 4237/4885HTT 4743/4885L3MBTL1 3238/4885
US-11912693-B2 Compounds for modulating S1P1 activity and methods of using the same S1PR1, S1PR2, S1PR3 SMN1; SMN2 1320/4885HTT 3156/4885L3MBTL1 3606/4885

“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.