SCHEMBL11014192

SCHEMBL11014192

c1ccc(CNCc2ccco2)cc1

nearest known ligand 0.71

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 3/20 0.71
KMT2A Q03164 3/20 0.71
ATM Q13315 1/20 0.64
CHRM2 P08172 1/20 0.56
POLB P06746 1/20 0.54
MAPT P10636 1/20 0.54
L3MBTL1 Q9Y468 1/20 0.54
TSHR P16473 1/20 0.53
GAA P10253 1/20 0.53
ALDH1A1 P00352 2/20 0.50
TDP1 Q9NUW8 1/20 0.50
CYP1A2 P05177 1/20 0.49
CYP2D6 P10635 1/20 0.49
TRPC4 Q9UBN4 1/20 0.48
TRPC5 Q9UL62 1/20 0.48
CTDSP1 Q9GZU7 1/20 0.47
KCNH3 Q9ULD8 1/20 0.47
LMNA P02545 1/20 0.47

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
SCHEMBL843371 0.87 CHRM2 (0.69) MEN1KMT2AATMCHRM2POLB
SCHEMBL22305089 0.86 KMT2A (0.68) MEN1KMT2AATMCHRM2POLB
Methane SCHEMBL28948442 0.85 CHRM2 (0.67) MEN1KMT2AATMCHRM2POLB
SCHEMBL8497081 0.85 MEN1 (0.62) MEN1KMT2AATMCHRM2POLB
SCHEMBL3425734 0.84 BCHE (0.71) MEN1KMT2AATMALDH1A1
SCHEMBL16523598 0.83 KMT2A (0.70) MEN1KMT2AATMCHRM2POLB
SCHEMBL29802812 0.83 CA12 (0.64) MEN1KMT2AATMCHRM2MAPT
SCHEMBL16523593 0.83 KMT2A (0.70) MEN1KMT2AATMCHRM2POLB
SCHEMBL31547203 0.83 MEN1 (0.70) MEN1KMT2AATMCHRM2POLB
SCHEMBL9483777 0.83 MAPT (0.58) MEN1KMT2AATMCHRM2MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122011028-A Method for efficiently preparing various substituted chiral phosphoramides 上海交通大学 2026-05-12 CN claimed
CN-119350180-A Industrial preparation method and application of high-purity alpha-aminonitrile 哈尔滨理工大学 2025-01-24 CN claimed
JP-57028011-A None JP disclosed
CN-122011028-A Method for efficiently preparing various substituted chiral phosphoramides 上海交通大学 2026-05-12 CN disclosed
WO-2025264680-A1 ANTICANCER POLYHETEROCYCLIC COMPOUNDS AND ASSOCIATED METHODS UNIVERSITY OF DENVER (US) 2025-12-26 WO disclosed
US-20250382302-A1 Anticancer polyheterocyclic compounds and associated methods UNIV OF DENVER (US) 2025-12-18 US disclosed
CN-119350180-A Industrial preparation method and application of high-purity alpha-aminonitrile 哈尔滨理工大学 2025-01-24 CN disclosed
US-11773064-B2 4-carboxamido-isoindolinone derivatives as selective PARP-1 inhibitors NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2023-10-03 US disclosed
CN-110818576-B Secondary amine derivative synthesized by rare earth catalysis and preparation method thereof 温州大学 2023-02-24 CN disclosed
US-20220363636-A1 4-CARBOXAMIDO-ISOINDOLINONE DERIVATIVES AS SELECTIVE PARP-1 INHIBITORS NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2022-11-17 US disclosed
US-11420940-B2 4-carboxamido-isoindolinone derivatives as selective parp-1 inhibitors NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2022-08-23 US disclosed
US-7235664-B2 Anthranilamides with heteroarylsulfonyl side chain, process of preparation, and use SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2007-06-26 US disclosed
US-7235664-B2 Anthranilamides with heteroarylsulfonyl side chain, process of preparation, and use SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2007-06-26 US disclosed
US-20070117807-A1 ANTHRANILAMIDES AND METHODS OF THEIR USE SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2007-05-24 US disclosed
US-20070117807-A1 ANTHRANILAMIDES AND METHODS OF THEIR USE SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2007-05-24 US disclosed
WO-2007009976-A1 POLYMERISATION CATALYST SYSTEM BASED ON MONOOXIME LIGANDS TOTAL PETROCHEMICALS RESEARCH FELUY (BE) 2007-01-25 WO disclosed
EP-1746112-A1 Polymerisation catalyst system based on monooxime ligands TOTAL PETROCHEMICALS RESEARCH FELUY (BE) 2007-01-24 EP disclosed
US-4508723-A 6-Azaoligocycloalkylmethyleneaminopenam compounds CIBA GEIGY CORPORATION (US) 1985-04-02 US disclosed
JP-S5728011-A PREPARATION OF AMINE USING SELENOPHENOL WAKO PURE CHEM IND LTD 1982-02-15 JP disclosed
EP-0005014-A1 Clavulanic acid derivatives, preparation and compositions BEECHAM GROUP PLC (GB) 1979-10-31 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 (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-11773064-B2 4-carboxamido-isoindolinone derivatives as selective PARP-1 inhibitors PARP1, PARP2, PARP12 MEN1 4521/4885KMT2A 1211/4885ATM 104/4885
US-11420940-B2 4-carboxamido-isoindolinone derivatives as selective parp-1 inhibitors PARP1, PARP2, PARP11 MEN1 4483/4885KMT2A 1614/4885ATM 160/4885
US-20220363636-A1 4-CARBOXAMIDO-ISOINDOLINONE DERIVATIVES AS SELECTIVE PARP-1 INHIBITORS PARP1, PARP2, PARP12 MEN1 4541/4885KMT2A 1196/4885ATM 102/4885
US-20250382302-A1 Anticancer polyheterocyclic compounds and associated methods HCCS, POLI, PARP1 MEN1 2192/4885KMT2A 2163/4885ATM 1873/4885
US-20070117807-A1 ANTHRANILAMIDES AND METHODS OF THEIR USE KCNH1, KCNH2, KCNJ2 MEN1 3308/4885KMT2A 587/4885ATM 2684/4885

“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.