SCHEMBL302457

SCHEMBL302457

Nc1ccccc1NC(=O)c1ccc(CN(C=O)OCc2cccnc2)cc1

nearest known ligand 0.63

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
HDAC1 Q13547 20/20 0.63
HDAC2 Q92769 11/20 0.63
HDAC3 O15379 10/20 0.63
HDAC11 Q96DB2 8/20 0.63
HDAC8 Q9BY41 8/20 0.63
HDAC6 Q9UBN7 8/20 0.63
HDAC4 P56524 7/20 0.63
HDAC7 Q8WUI4 7/20 0.63
HDAC10 Q969S8 7/20 0.63
HDAC9 Q9UKV0 7/20 0.63
HDAC5 Q9UQL6 7/20 0.63
NCOR2 Q9Y618 3/20 0.63
CYP3A4 P08684 2/20 0.63
KDM1A O60341 1/20 0.63
F3 P13726 1/20 0.63
NAMPT P43490 3/20 0.56
KCNH2 Q12809 1/20 0.50
NCOR1 O75376 1/20 0.49

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
Bromide SCHEMBL2409900 0.99 HDAC1 (0.62) HDAC1HDAC2HDAC3HDAC11HDAC8
Hydrochloric Acid SCHEMBL2407989 0.99 HDAC1 (0.62) HDAC1HDAC2HDAC3HDAC11HDAC8
SCHEMBL2411926 0.91 HDAC1 (0.62) HDAC1HDAC2HDAC3HDAC11HDAC8
SCHEMBL3559032 0.89 HDAC1 (0.62) HDAC1HDAC2HDAC3HDAC11HDAC8
SCHEMBL2412810 0.89 HDAC1 (0.55) HDAC1HDAC2HDAC3HDAC11HDAC8
SCHEMBL2413630 0.88 HDAC1 (0.66) HDAC1HDAC2HDAC3HDAC11HDAC8
SCHEMBL2416256 0.88 HDAC1 (0.66) HDAC1HDAC2HDAC3HDAC11HDAC8
SCHEMBL2411259 0.88 HDAC1 (0.56) HDAC1HDAC2HDAC3HDAC11HDAC8
SCHEMBL2416730 0.87 HDAC1 (0.50) HDAC1HDAC2HDAC3HDAC11HDAC8
SCHEMBL2410013 0.87 HDAC1 (0.67) HDAC1HDAC2HDAC3HDAC11HDAC8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-RE45499-E1 N-(2-aminophenyl)-4-[N-(pyridine-3-yl)-methoxycarbonyl-aminomethyl]-benzamide (MS-275) polymorph B BAYER INTELLECTUAL PROPERTY GMBH (DE) 2015-04-28 US claimed
CN-102137846-B N-(2-aminophenyl)-4-[N-(pyridine-3-yl)-methoxycarbonyl-aminomethyl]-benzamide (MS-275)polymorph B BAYER SCHERING PHARMA AG 2014-04-23 CN claimed
JP-2012500819-A 2012-01-12 JP claimed
EP-2350005-B1 N-(2-AMINOPHENYL)-4-[N-(PYRIDINE-3-YL)-METHOXYCARBONYL-AMINOMETHYL]-BENZAMIDE (MS-275)POLYMORPH B Bayer Pharma AG (DE) 2011-12-21 EP claimed
EP-2350005-A1 N-(2-AMINOPHENYL)-4-[N-(PYRIDINE-3-YL)-METHOXYCARBONYL-AMINOMETHYL]-BENZAMIDE (MS-275)POLYMORPH B Bayer Schering Pharma Aktiengesellschaft (DE) 2011-08-03 EP claimed
CN-102137846-A N-(2-aminophenyl)-4-[N-(pyridine-3-yl)-methoxycarbonyl-aminomethyl]-benzamide (MS-275)polymorph b BAYER SCHERING PHARMA AG 2011-07-27 CN claimed
US-7973166-B2 N-(2-aminophenyl)-4-[N-(pyridine-3-yl)-methoxycarbonyl-aminomethyl]-benzamide (MS-275) polymorph B BAYER SCHERING PHARMA AG (DE) 2011-07-05 US claimed
US-20100056585-A1 N-(2-Aminophenyl)-4-[N-(Pyridine-3-yl)-Methoxycarbonyl-Aminomethyl]-Benzamide (MS-275) Polymorph B BAYER SCHERING PHARMA AG (DE) 2010-03-04 US claimed
WO-2010022988-A1 N-(2-AMINOPHENYL)-4-[N-(PYRIDINE-3-YL)-METHOXYCARBONYL-AMINOMETHYL]-BENZAMIDE (MS-275)POLYMORPH B BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2010-03-04 WO claimed
US-20050215601-A1 Therapeutic agent for rheumatic disease comprising benzamide derivative as active ingredient SANTEN PHARMACEUTICAL CO., LTD. (JP) 2005-09-29 US claimed
EP-1547585-A1 THERAPEUTIC AGENT FOR RHEUMATISM CONTAINING BENZAMIDE DERIVATIVE AS ACTIVE INGREDIENT SANTEN PHARMACEUTICAL CO., LTD. (JP) 2005-06-29 EP claimed
US-12168054-B2 Method of treating cancer using a combination of entinostat and an anti-CSF-1R antibody SYNDAX PHARMACEUTICALS, INC. (US) 2024-12-17 US disclosed
US-20240288425-A1 SELECTION OF PATIENTS FOR COMBINATION THERAPY SYNDAX PHARMACEUTICALS, INC. 2024-08-29 US disclosed
US-12000829-B2 Selection of patients for combination therapy SYNDAX PHARMACEUTICALS, INC. (US) 2024-06-04 US disclosed
EP-3270966-B1 COMBINATION OF HDAC INHIBITOR AND ANTI-PD-1 ANTIBODY FOR TREATMENT OF CANCER WHEREIN THE COMBINATION DOES NOT COMPRISE 5-AZACYTIDINE. SYNDAX PHARMACEUTICALS INC (US) 2024-05-01 EP disclosed
WO-2004058234-A2 PHARMACEUTICAL COMBINATIONS OF PHTHALAZINE VEGF INHIBITORS AND BENZAMIDE HDAC INHIBITORS SCHERING AKTIENGESELLSCHAFT (DE) 2004-07-15 WO disclosed
EP-1437346-A1 Benzamide derivatives useful as cell differentiation inducers Schering AG (DE) 2004-07-14 EP disclosed
EP-0847992-B1 Benzamide derivatives, useful as cell differentiation inducers SCHERING AG (DE) 2004-06-23 EP disclosed
US-6174905-B1 AS CARCINOSTATIC AGENT TO A HEMATOLOGIC MALIGNANCY AND A SOLID CARCINOMA MITSUI CHEMICALS, INC. (JP) 2001-01-16 US disclosed
EP-0847992-A1 Benzamide derivatives, useful as cell differentiation inducers Mitsui Chemicals, Inc. (JP) 1998-06-17 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-20240288425-A1 SELECTION OF PATIENTS FOR COMBINATION THERAPY CD14, CD74, HDAC1 HDAC1 3/4885HDAC2 7/4885HDAC3 6/4885
US-20050215601-A1 Therapeutic agent for rheumatic disease comprising benzamide derivative as active ingredient SSB, HRH2, TYR HDAC1 13/4885HDAC2 17/4885HDAC3 88/4885
US-12000829-B2 Selection of patients for combination therapy CD14, CD74, HDAC1 HDAC1 3/4885HDAC2 7/4885HDAC3 6/4885
US-20100056585-A1 N-(2-Aminophenyl)-4-[N-(Pyridine-3-yl)-Methoxycarbonyl-Aminomethyl]-Benzamide (MS-275) Polymorph B CYP3A5, MRPS35, NNMT HDAC1 482/4885HDAC2 767/4885HDAC3 1186/4885
US-12168054-B2 Method of treating cancer using a combination of entinostat and an anti-CSF-1R antibody CSF3R, CSF1R, HDAC1 HDAC1 3/4885HDAC2 7/4885HDAC3 12/4885

“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.