SCHEMBL4575540

SCHEMBL4575540

CNc1ccccc1Cc1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 3/20 0.58
LMNA P02545 2/20 0.49
HTT P42858 1/20 0.49
DRD3 P35462 1/20 0.49
CALM1 P0DP23 1/20 0.48
PKM P14618 1/20 0.47
HTR2A P28223 1/20 0.47
KDM4E B2RXH2 2/20 0.46
MAPT P10636 2/20 0.46
ALDH1A1 P00352 2/20 0.46
USP2 O75604 1/20 0.46
POLB P06746 1/20 0.46
HPGD P15428 1/20 0.46
RECQL P46063 1/20 0.46
NPSR1 Q6W5P4 1/20 0.46
HSD17B10 Q99714 1/20 0.46
TDP1 Q9NUW8 1/20 0.46
BCL2 P10415 1/20 0.45
BCL2L1 Q07817 1/20 0.45
HRH1 P35367 1/20 0.44

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
SCHEMBL27620900 0.84 L3MBTL1 (0.55) L3MBTL1LMNAHTTDRD3CALM1
SCHEMBL5426523 0.84 L3MBTL1 (0.47) L3MBTL1LMNAHTTDRD3CALM1
SCHEMBL14292157 0.83 ATM (0.48) L3MBTL1LMNAHTTKDM4EMAPT
SCHEMBL27937954 0.82 L3MBTL1 (0.46) L3MBTL1LMNAHTTDRD3CALM1
SCHEMBL2870268 0.81 L3MBTL1 (0.53) L3MBTL1LMNAHTTDRD3CALM1
SCHEMBL27938009 0.81 L3MBTL1 (0.45) L3MBTL1LMNAHTTDRD3CALM1
SCHEMBL2137543 0.80 L3MBTL1 (0.56) L3MBTL1LMNAHTTDRD3CALM1
SCHEMBL28268501 0.80 L3MBTL1 (0.51) L3MBTL1LMNAHTTDRD3CALM1
SCHEMBL10423678 0.80 L3MBTL1 (0.51) L3MBTL1LMNAHTTDRD3CALM1
SCHEMBL1506234 0.80 L3MBTL1 (0.56) L3MBTL1LMNAHTTDRD3CALM1

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
EP-4430036-A2 BCAT2 INHIBITORS Agios Pharmaceuticals, Inc. (US) 2024-09-18 EP disclosed
WO-2023086539-A2 BCAT2 INHIBITORS AGIOS PHARMACEUTICALS, INC. (US) 2023-05-19 WO disclosed
CN-108069957-B Prolyl hydroxylase inhibitors and uses thereof 广东东阳光药业有限公司 2022-11-04 CN disclosed
EP-3752510-A1 MACROCYCLES AS MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR, PHARMACEUTICAL COMPOSITIONS THEREOF, THEIR USE IN THE TREATMENT OF CYCSTIC FIBROSIS, AND PROCESS FOR MAKING THEM Vertex Pharmaceuticals Incorporated (US) 2020-12-23 EP disclosed
EP-3731869-A1 IRAK DEGRADERS AND USES THEREOF Kymera Therapeutics, Inc. (US) 2020-11-04 EP disclosed
WO-2019161078-A1 MACROCYCLES AS MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR, PHARMACEUTICAL COMPOSITIONS THEREOF, THEIR USE IN THE TREATMENT OF CYCSTIC FIBROSIS, AND PROCESS FOR MAKING THEM VERTEX PHARMACEUTICALS INCORPORATED (US) 2019-08-22 WO disclosed
EP-3519464-A1 THIOUREA GROUP IV TRANSITION METAL CATALYSTS AND POLYMERIZATION SYSTEMS Dow Global Technologies LLC (US) 2019-08-07 EP disclosed
WO-2018063799-A1 THIOUREA GROUP IV TRANSITION METAL CATALYSTS AND POLYMERIZATION SYSTEMS DOW GLOBAL TECHNOLOGIES LLC (US) 2018-04-05 WO disclosed
EP-2780026-A2 HCV NS3 PROTEASE INHIBITORS Merck Sharp & Dohme Corp. (US) 2014-09-24 EP disclosed
EP-2705028-A1 PROCESS FOR THE PREPARATION OF A RIVAROXABAN AND INTERMEDIATES FORMED IN SAID PROCESS Egis Gyógyszergyár Nyilvánosan Müködö Részvény-Társaság (HU) 2014-03-12 EP disclosed
US-20090143351-A1 SUBSTITUTED AZETIDINONES DAIAMED (US) 2009-06-04 US disclosed
US-7501404-B2 Substituted azetidinones DAIMED (US) 2009-03-10 US disclosed
EP-1948670-A1 METHOD OF SEPARATING ACIDS FROM CHEMICAL REACTION MIXTURES BY MEANS OF APOLAR AMINES BASF SE (DE) 2008-07-30 EP disclosed
US-20080004290-A1 Anti-Cancer Agents THE UNIVERSITY OF QUEENSLAND (AU) 2008-01-03 US disclosed
US-20080004290-A1 Anti-Cancer Agents THE UNIVERSITY OF QUEENSLAND (AU) 2008-01-03 US disclosed
WO-2007054392-A1 METHOD OF SEPARATING ACIDS FROM CHEMICAL REACTION MIXTURES BY MEANS OF APOLAR AMINES BASF SE (DE) 2007-05-18 WO disclosed
US-20070105832-A1 Substituted azetidinones Cadrenal Therapeutics, Inc. 2007-05-10 US disclosed
EP-1615644-B1 SUBSTITUTED 4-PHENYL-4-[1H-IMIDAZOL-2-YL]-PIPERIDINE DERIVATIVES AND THEIR USE AS SELECTIVE NON-PEPTIDE DELTA OPIOID AGONISTS WITH ANTIDEPRESSANT AND ANXIOLYTIC ACTIVITY JANSSEN PHARMACEUTICA NV (BE) 2007-02-14 EP disclosed
CN-1531425-A Urea derivatives as integrin alpha 4 antagonists ������ҩ�����޹�˾ 2004-09-22 CN disclosed
US-4025467-A CONVERSION OF COVALENT CHLORINE TO IONIC CHLORIDE ROHM AND HAAS COMPANY (US) 1977-05-24 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 (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-20070105832-A1 Substituted azetidinones F2R, CPA3, CFD L3MBTL1 4390/4885LMNA 1127/4885HTT 3188/4885
US-20090143351-A1 SUBSTITUTED AZETIDINONES F2R, CPA3, CFD L3MBTL1 4390/4885LMNA 1127/4885HTT 3188/4885
US-20080004290-A1 Anti-Cancer Agents TP53, TOP2A, MCL1 L3MBTL1 3038/4885LMNA 2557/4885HTT 4513/4885

“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.