SCHEMBL543706

SCHEMBL543706

O=C(CN1C(=O)c2ccccc2C1=O)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
GSK3B P49841 1/20 0.75
SMN1; SMN2 Q16637 3/20 0.69
KDM4E B2RXH2 2/20 0.69
TP53 P04637 1/20 0.69
L3MBTL1 Q9Y468 1/20 0.69
CA12 O43570 2/20 0.69
CA9 Q16790 1/20 0.69
NPC1 O15118 2/20 0.69
ALDH1A1 P00352 4/20 0.57
KMT2A Q03164 4/20 0.57
MEN1 O00255 2/20 0.57
CYP1A2 P05177 1/20 0.57
CYP2C9 P11712 1/20 0.57
RAB9A P51151 3/20 0.55
MAPT P10636 1/20 0.54
NPSR1 Q6W5P4 1/20 0.54
ALOX15 P16050 1/20 0.53
HSD17B10 Q99714 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
SCHEMBL30546567 1.00 GSK3B (0.75) GSK3BSMN1; SMN2KDM4ETP53L3MBTL1
Methane SCHEMBL11813940 0.98 GSK3B (0.73) GSK3BSMN1; SMN2KDM4ETP53L3MBTL1
SCHEMBL1906596 0.87 GSK3B (0.73) GSK3BSMN1; SMN2KDM4ETP53L3MBTL1
SCHEMBL694554 0.86 GSK3B (0.71) GSK3BSMN1; SMN2KDM4ETP53L3MBTL1
SCHEMBL696173 0.86 GSK3B (0.71) GSK3BSMN1; SMN2KDM4ETP53L3MBTL1
SCHEMBL14711680 0.86 GSK3B (1.00) GSK3BSMN1; SMN2KDM4ETP53L3MBTL1
SCHEMBL10671594 0.84 CA12 (0.59) GSK3BSMN1; SMN2KDM4ETP53L3MBTL1
SCHEMBL29236638 0.83 GSK3B (0.68) GSK3BSMN1; SMN2KDM4ETP53L3MBTL1
SCHEMBL401800 0.82 GSK3B (0.57) GSK3BSMN1; SMN2KDM4ETP53L3MBTL1
SCHEMBL1609678 0.82 SMN1; SMN2 (0.62) GSK3BSMN1; SMN2KDM4ETP53L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4707276-A2 MALT1 MODULATORS AND USES THEREOF Rarefied Biosciences, Inc. (US) 2026-03-11 EP disclosed
EP-4499611-B1 MALT1 MODULATORS AND USES THEREOF RAREFIED BIOSCIENCES INC (US) 2026-02-18 EP disclosed
US-20250326738-A1 MALT1 Modulators and Uses Thereof RAREFIED BIOSCIENCES, INC. (US) 2025-10-23 US disclosed
EP-3891158-B1 MAP4K4 INHIBITORS IMPERIAL COLLEGE INNOVATIONS LTD (GB) 2025-09-10 EP disclosed
US-12247045-B2 MAP4K4 inhibitors IMPERIAL COLLEGE INNOVATIONS LIMITED (GB) 2025-03-11 US disclosed
US-20240199621-A1 MAP4K4 INHIBITORS IMPERIAL COLLEGE INNOVATIONS LTD (GB) 2024-06-20 US disclosed
CN-118184477-A Method for preparing chiral amino alcohol compound by catalyzing amino ketone with nickel metal by using water as hydrogen source 云南民族大学 2024-06-14 CN disclosed
CN-112585147-B MAP4K4 inhibitors 帝国理工学院创新有限公司 2023-12-05 CN disclosed
US-11795169-B2 MAP4K4 inhibitors IMPERIAL COLLEGE INNOVATIONS LIMITED (GB) 2023-10-24 US disclosed
US-11795169-B2 MAP4K4 inhibitors IMPERIAL COLLEGE INNOVATIONS LIMITED (GB) 2023-10-24 US disclosed
EP-0061178-B1 NOVEL 1,2-DIHYDROPYRIDO(3,4-B)-PYRAZINES AND METHOD FOR PREPARING SAME Southern Research Institute (US) 1986-02-26 EP disclosed
EP-0172147-A2 Amide derivatives of 2-(p-aminobenzyl)-butyric acid and esters thereof having hypolipidemizing activity Medosan Industrie Biochimiche Riunite S.r.l. (IT) 1986-02-19 EP disclosed
EP-0151765-A2 Novel intermediates in a process for making novel 1,2-dihydropyrido(3,4-b)-pyrazines Southern Research Institute (US) 1985-08-21 EP disclosed
US-4511721-A Intermediate for preparing antifungal 1,2-dihydropyrido[3,4-b]-pyrazines SOUTHERN RESEARCH INSTITUTE (US) 1985-04-16 US disclosed
US-4453003-A ENZYME INHIBITORS, ANTIINFLAMMATORY AGENTS UMEZAWA HAMAO (JP) 1984-06-05 US disclosed
US-4450160-A ANTIDEPRESSANTS SOUTHERN RESEARCH INSTITUTE (US) 1984-05-22 US disclosed
US-4410618-A DEVELOPMENT INHIBITORS EASTMAN KODAK COMPANY (US) 1983-10-18 US disclosed
US-4391986-A Process for producing threo-3-amino-2-hydroxybutanoyl-aminoacetic acids, as well as novel intermediates therefor and process for producing them NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1983-07-05 US disclosed
EP-0061178-A2 Novel 1,2-dihydropyrido(3,4-b)-pyrazines and method for preparing same Southern Research Institute (US) 1982-09-29 EP disclosed
US-4281180-A Process for producing threo-3-amino-2-hydroxybutanoyl-aminoacetic acids, as well as novel intermediated therefor and process for producing them NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1981-07-28 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 (4 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-20250326738-A1 MALT1 Modulators and Uses Thereof MALT1, SQSTM1, PPP1R10 GSK3B 534/4885SMN1; SMN2 2034/4885KDM4E 2044/4885
US-12247045-B2 MAP4K4 inhibitors MAP4K4, MAP4K5, MAP4K1 GSK3B 300/4885SMN1; SMN2 2995/4885KDM4E 1003/4885
US-11795169-B2 MAP4K4 inhibitors MAP4K4, MAP4K2, MAP4K5 GSK3B 493/4885SMN1; SMN2 3315/4885KDM4E 742/4885
US-20240199621-A1 MAP4K4 INHIBITORS MAP4K4, MAP4K2, MAP4K5 GSK3B 493/4885SMN1; SMN2 3315/4885KDM4E 742/4885

“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.