SCHEMBL8444248

SCHEMBL8444248

O=C(O)c1ccccc1Nc1cccc2c1C(=O)c1ccccc1C2=O

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 3/20 0.68
▸ L3MBTL1 Q9Y468 2/20 0.68
▸ FABP4 P15090 7/20 0.59
▸ FABP3 P05413 3/20 0.59
▸ FABP5 Q01469 3/20 0.59
▸ MAPT P10636 6/20 0.58
▸ KMT2A Q03164 4/20 0.58
▸ KDM4E B2RXH2 2/20 0.58
▸ APAF1 O14727 1/20 0.58
▸ TDP2 O95551 1/20 0.58
▸ CASP3 P42574 1/20 0.58
▸ HKDC1 Q2TB90 1/20 0.58
▸ SENP8 Q96LD8 1/20 0.58
▸ SENP7 Q9BQF6 1/20 0.58
▸ SENP6 Q9GZR1 1/20 0.58
▸ RXFP1 Q9HBX9 1/20 0.58
▸ SAE1 Q9UBE0 1/20 0.58
▸ UBA2 Q9UBT2 1/20 0.58
▸ LMNA P02545 3/20 0.58
▸ MAOA P21397 1/20 0.56

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
SCHEMBL29967042 0.97 FABP4 (0.63) ALDH1A1L3MBTL1FABP4FABP3FABP5
SCHEMBL5187548 0.97 FABP4 (0.63) ALDH1A1L3MBTL1FABP4FABP3FABP5
SCHEMBL11602683 0.95 FABP4 (0.61) ALDH1A1L3MBTL1FABP4FABP3FABP5
SCHEMBL13065508 0.88 CDC25B (0.59) ALDH1A1L3MBTL1FABP4FABP3FABP5
SCHEMBL16784748 0.87 FABP4 (0.53) ALDH1A1L3MBTL1FABP4FABP3FABP5
SCHEMBL13021513 0.87 FABP4 (0.56) ALDH1A1L3MBTL1FABP4FABP3FABP5
SCHEMBL11849832 0.87 MAPT (0.54) ALDH1A1L3MBTL1FABP4FABP3FABP5
SCHEMBL9170104 0.85 ALDH1A1 (0.52) ALDH1A1L3MBTL1FABP4FABP3MAPT
SCHEMBL42481 0.85 MAPT (0.71) ALDH1A1L3MBTL1MAPTKMT2AKDM4E
SCHEMBL29438168 0.85 MAPT (0.71) ALDH1A1L3MBTL1MAPTKMT2AKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0576995-B1 Process for the preparation of 5-halogeno-2-(1-anthraquinonylamino)benzoic acids and of 4'-halogeno-2,1(N)-anthraquinonyl-1',2'(N)-benzacridones BASF AG (DE) 1997-09-17 — — EP claimed
US-5401846-A Synthesis of vat dyes BASF AKTIENGESELLSCHAFT (DE) 1995-03-28 — — US claimed
JP-6065170-A — — None — — JP disclosed
US-20070232622-A1 Small molecule toll-like receptor (TLR) antagonists COLEY PHARMACEUTICAL GMBH (DE) 2007-10-04 — — US disclosed
US-20070232622-A1 Small molecule toll-like receptor (TLR) antagonists COLEY PHARMACEUTICAL GMBH (DE) 2007-10-04 — — US disclosed
CN-1245516-A Method for preparing light-absorbing polymer composition EASTMAN CHEM CO (US) 2000-02-23 — — CN disclosed
EP-0948570-A1 METHOD FOR PREPARING LIGHT-ABSORBING POLYMERIC COMPOSITIONS EASTMAN CHEMICAL COMPANY (US) 1999-10-13 — — EP disclosed
WO-1998048769-A1 UV-CURABLE NAIL COATING FORMULATIONS CONTAINING CELLULOSE ESTERS WITH ETHYLENICALLY UNSATURATED PENDANT GROUPS EASTMAN CHEMICAL COMPANY (US) 1998-11-05 — — WO disclosed
WO-1998023690-A9 METHOD FOR PREPARING LIGHT-ABSORBING POLYMERIC COMPOSITIONS — 1998-09-17 — — WO disclosed
WO-1998023690-A1 METHOD FOR PREPARING LIGHT-ABSORBING POLYMERIC COMPOSITIONS EASTMAN CHEMICAL COMPANY (US) 1998-06-04 — — WO disclosed
EP-0703945-A1 CELLULOSE ESTER BLENDS EASTMAN CHEMICAL COMPANY (US) 1996-04-03 — — EP disclosed
US-5401846-A Synthesis of vat dyes BASF AKTIENGESELLSCHAFT (DE) 1995-03-28 — — US disclosed
US-5401846-A Synthesis of vat dyes BASF AKTIENGESELLSCHAFT (DE) 1995-03-28 — — US disclosed
WO-1994028062-A1 CELLULOSE ESTER BLENDS EASTMAN CHEMICAL COMPANY (US) 1994-12-08 — — WO disclosed
JP-H0665170-A PREPARATION OF 5-HALOGEN-2-(1-ANTHRAQUINONYLAMINO) BENZOIC ACID AND 4'-HALOGEN-2,1(N)-ANTHRAQUINONYL-1',2'(N) BENZACRIDONE BASF AG 1994-03-08 — — JP disclosed
EP-0576995-A2 Process for the preparation of 5-halogeno-2-(1-anthraquinonylamino)benzoic acids and of 4'-halogeno-2,1(N)-anthraquinonyl-1',2'(N)-benzacridones BASF Aktiengesellschaft (DE) 1994-01-05 — — EP disclosed
EP-0570511-A1 THERMOPLASTIC POLYMERS COLORED WITH POLYESTER COLOR CONCENTRATES EASTMAN CHEMICAL COMPANY (US) 1993-11-24 — — EP disclosed
EP-0525073-A1 ANTHRAQUINONES AS INHIBITORS OF SULFIDE PRODUCTION FROM SULFATE-REDUCING BACTERIA. DU PONT (US) 1993-02-03 — — EP disclosed
WO-1992013921-A1 THERMOPLASTIC POLYMERS COLORED WITH POLYESTER COLOR CONCENTRATES EASTMAN KODAK COMPANY (US) 1992-08-20 — — WO disclosed
WO-1991015954-A1 ANTHRAQUINONES AS INHIBITORS OF SULFIDE PRODUCTION FROM SULFATE-REDUCING BACTERIA E.I. DU PONT DE NEMOURS AND COMPANY (US) 1991-10-31 — — WO 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-20070232622-A1 Small molecule toll-like receptor (TLR) antagonists TLR3, TLR8, TLR7 ALDH1A1 4582/4885L3MBTL1 792/4885FABP4 3034/4885

“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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