SCHEMBL1164427

SCHEMBL1164427

Cc1ccc(N2C(=O)C=CC2=O)cc1C

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MGLL Q99685 11/20 0.59
▸ FAAH O00519 4/20 0.58
▸ KMT2A Q03164 4/20 0.58
▸ MEN1 O00255 3/20 0.58
▸ HSP90AA1 P07900 4/20 0.57
▸ ALDH1A1 P00352 3/20 0.54
▸ NPSR1 Q6W5P4 3/20 0.54
▸ CCR6 P51684 2/20 0.54
▸ MAPT P10636 2/20 0.54
▸ G6PD P11413 2/20 0.54
▸ PKM P14618 1/20 0.54
▸ HPGD P15428 1/20 0.54
▸ MCL1 Q07820 1/20 0.54
▸ L3MBTL1 Q9Y468 1/20 0.54
▸ GAA P10253 1/20 0.51
▸ TSHR P16473 2/20 0.50
▸ NPC1 O15118 1/20 0.50
▸ MAPK1 P28482 1/20 0.50
▸ CASP1 P29466 1/20 0.50
▸ RAB9A P51151 1/20 0.50

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
SCHEMBL30435094 1.00 MGLL (0.59) MGLLFAAHKMT2AMEN1HSP90AA1
SCHEMBL22399177 0.85 MGLL (0.57) MGLLFAAHKMT2AMEN1HSP90AA1
SCHEMBL29898506 0.83 TLR9 (0.61) MGLLFAAHHSP90AA1NPSR1CCR6
SCHEMBL1741609 0.83 TLR9 (0.61) MGLLFAAHHSP90AA1NPSR1CCR6
SCHEMBL94095 0.83 MGLL (0.57) MGLLFAAHHSP90AA1NPSR1CCR6
SCHEMBL13405900 0.82 KMT2A (0.62) KMT2AMEN1ALDH1A1NPSR1MAPT
SCHEMBL21495979 0.82 MGLL (0.53) MGLLFAAHHSP90AA1ALDH1A1NPSR1
SCHEMBL8005849 0.82 PKM (0.58) MGLLFAAHKMT2AMEN1HSP90AA1
SCHEMBL30198527 0.82 PKM (0.58) MGLLFAAHKMT2AMEN1HSP90AA1
SCHEMBL3180754 0.82 TSHR (0.54) MGLLFAAHHSP90AA1NPSR1CCR6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112358479-B Synthesis method of pyrrolo [3,4-c ] quinoline-1, 3-dione compound 西北师范大学 2023-06-16 — — CN disclosed
CN-113307995-B Temperature-resistant thermoplastic polyurethane film and preparation method thereof 苏州市雄林新材料科技有限公司 2023-04-14 — — CN disclosed
CN-109971130-B Cyanate ester resin composition and use thereof 广东生益科技股份有限公司 2021-12-17 — — CN disclosed
CN-112358479-A Synthesis method of pyrrolo [3,4-c ] quinoline-1, 3-diketone compound 西北师范大学 2021-02-12 — — CN disclosed
US-20130025495-A1 COMPOSITIONS COMPRISING A REACTIVE MONOMER AND USES THEREOF ISP INVESTMENTS INC. (US) 2013-01-31 — — US disclosed
US-20130025495-A1 COMPOSITIONS COMPRISING A REACTIVE MONOMER AND USES THEREOF ISP INVESTMENTS INC. (US) 2013-01-31 — — US disclosed
EP-2467694-A1 USE OF A BIS-MALEIC ANHYDRIDE CROSS-LINKING AGENT FOR FIXATION OF A CELL OR TISSUE SAMPLE Roche Diagnostics GmbH (DE) 2012-06-27 — — EP disclosed
WO-2011020612-A1 USE OF A BIS-MALEIC ANHYDRIDE CROSS-LINKING AGENT FOR FIXATION OF A CELL OR TISSUE SAMPLE ROCHE DIAGNOSTICS GMBH (DE) 2011-02-24 — — WO disclosed
US-5314950-A Molding materials, colorfastness, compatibility with acrylonitrile-styrene resins CYTEC TECHNOLOGY CORP. (US) 1994-05-24 — — 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 (1 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-20130025495-A1 COMPOSITIONS COMPRISING A REACTIVE MONOMER AND USES THEREOF MEP1A, MACF1, CYP1B1 MGLL 1404/4885FAAH 2247/4885KMT2A 2245/4885

“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.

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