SCHEMBL312344

SCHEMBL312344

O=C(O)CCCCCCC(=O)Nc1ccccc1

nearest known ligand 0.77

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC4 P56524 17/20 0.77
HDAC1 Q13547 17/20 0.77
HDAC7 Q8WUI4 17/20 0.77
HDAC11 Q96DB2 17/20 0.77
HDAC8 Q9BY41 17/20 0.77
HDAC6 Q9UBN7 17/20 0.77
HDAC9 Q9UKV0 17/20 0.77
HDAC5 Q9UQL6 17/20 0.77
HDAC3 O15379 16/20 0.77
HDAC2 Q92769 16/20 0.77
HDAC10 Q969S8 16/20 0.77
NCOR1 O75376 2/20 0.77
NCOR2 Q9Y618 2/20 0.77
KDM4E B2RXH2 1/20 0.77
BRD4 O60885 1/20 0.77
NR1I2 O75469 1/20 0.77
EGFR P00533 1/20 0.77
CYP3A4 P08684 1/20 0.77
LTA4H P09960 1/20 0.77
NR0B1 P51843 1/20 0.77

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
SCHEMBL1064861 1.00 HDAC4 (0.77) HDAC4HDAC1HDAC7HDAC11HDAC8
SCHEMBL1060805 0.98 HDAC4 (0.73) HDAC4HDAC1HDAC7HDAC11HDAC8
SCHEMBL3806017 0.94 MEN1 (0.73) HDAC4HDAC1HDAC7HDAC11HDAC8
SCHEMBL6669511 0.94 HDAC4 (0.85) HDAC4HDAC1HDAC7HDAC11HDAC8
SCHEMBL6665592 0.94 HDAC4 (0.85) HDAC4HDAC1HDAC7HDAC11HDAC8
SCHEMBL137348 0.94 HDAC4 (0.85) HDAC4HDAC1HDAC7HDAC11HDAC8
SCHEMBL1065393 0.94 HDAC4 (0.85) HDAC4HDAC1HDAC7HDAC11HDAC8
SCHEMBL517309 0.92 HDAC4 (0.81) HDAC4HDAC1HDAC7HDAC11HDAC8
Hydroxyamine SCHEMBL1268824 0.90 HDAC6 (0.79) HDAC4HDAC1HDAC7HDAC11HDAC8
SCHEMBL6296181 0.88 HDAC4 (0.75) HDAC4HDAC1HDAC7HDAC11HDAC8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2011061545-A1 HPLC METHOD FOR ANALYZING VORINOSTAT GENERICS [UK] LIMITED (GB) 2011-05-26 WO claimed
WO-2026102197-A1 METHODS FOR PREPARING HIGH-PURITY VORINOSTAT AND PRECURSORS THEREOF UNRAVEL BIOSCIENCES, INC. (US) 2026-05-15 WO disclosed
US-20260125343-A1 METHODS FOR PREPARING HIGH-PURITY VORINOSTAT AND PRECURSORS THEREOF UNRAVEL BIOSCIENCES INC (US) 2026-05-07 US disclosed
CN-121926915-A Application of 7-phenylcarbamoyl heptanoic acid in preparation of antitumor drugs 山东大学 2026-04-28 CN disclosed
CN-121926915-A Application of 7-phenylcarbamoyl heptanoic acid in preparation of antitumor drugs 山东大学 2026-04-28 CN disclosed
WO-2024218227-A1 INDOLE DERIVATIVES AS HISTONE DEACETYLASE (HDAC) INHIBITORS FOR THE TREATMENT OF CANCER UNIVERSIDAD DE ALCALÁ (ES) 2024-10-24 WO disclosed
EP-4450494-A1 INDOLE DERIVATIVES AS HISTONE DEACETYLASE (HDAC) INHIBITORS FOR THE TREATMENT OF CANCER Consejo Superior De Investigaciones Científicas (ES) 2024-10-23 EP disclosed
EP-3724192-B1 TRIAZOLOBENZAZEPINES AS VASOPRESSIN V1A RECEPTOR ANTAGONISTS RICHTER GEDEON NYRT (HU) 2022-08-03 EP disclosed
US-11298363-B2 Triazolobenzazepines as vasopressin V1a receptor antagonists RICHTER GEDEON NYRT. (HU) 2022-04-12 US disclosed
US-11046715-B2 Boronic derivatives of hydroxamates as anticancer agents XAVIER UNIVERSITY OF LOUISIANA (US) 2021-06-29 US disclosed
US-20070117815-A1 Method of treating cancers with SAHA and pemetrexed MERCK & CO., INC. 2007-05-24 US disclosed
US-20070060614-A1 Methods of treating cancer with hdac inhibitors NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2007-03-15 US disclosed
WO-2006127321-A2 FORMULATIONS OF SUBEROYLANILIDE HYDROXAMIC ACID AND METHODS FOR PRODUCING SAME MERCK & CO., INC. (US) 2006-11-30 WO disclosed
WO-2006127319-A2 FORMULATIONS OF SUBEROYLANILIDE HYDROXAMIC ACID AND METHODS FOR PRODUCING SAME MERCK & CO., INC. (US) 2006-11-30 WO disclosed
EP-1692097-A1 TRICYCLIC HYDROXAMATE AND BENZAMIDE DERIVATIVES, COMPOSITIONS AND METHODS Exonhit Therapeutics SA (FR) 2006-08-23 EP disclosed
US-20060167103-A1 Methods of treating cancer with HDAC inhibitors ATON PHARMA, INC. (US) 2006-07-27 US disclosed
WO-2005058803-A1 TRICYCLIC HYDROXAMATE AND BENZAMIDE DERIVATIVES, COMPOSITIONS AND METHODS EXONHIT THERAPEUTICS SA (FR) 2005-06-30 WO disclosed
EP-1541549-A1 Tricyclic hydroxamate and benzaminde derivatives, compositions and methods Exonhit Therapeutics S.A. (FR) 2005-06-15 EP disclosed
US-20040132825-A1 Methods of treating cancer with HDAC inhibitors NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2004-07-08 US disclosed
US-20040127523-A1 safe, daily dosing regimen of histone deacetylase (HDAC) inhibitors having favorable pharmacokinetic profiles such as high bioavailability and surprisingly give rise to high blood levels of the active compounds over an extended period of time NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2004-07-01 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 (8 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-20060167103-A1 Methods of treating cancer with HDAC inhibitors HDAC5, HDAC1, HDAC4 HDAC4 3/4885HDAC1 2/4885HDAC7 5/4885
US-20040127523-A1 safe, daily dosing regimen of histone deacetylase (HDAC) inhibitors having favorable pharmacokinetic profiles such as high bioavailability and surprisingly give rise to high blood levels of the active compounds over an extended period of time HDAC1, HDAC5, HDAC9 HDAC4 5/4885HDAC1 1/4885HDAC7 10/4885
US-20070117815-A1 Method of treating cancers with SAHA and pemetrexed HDAC5, HDAC1, HDAC4 HDAC4 3/4885HDAC1 2/4885HDAC7 7/4885
US-20040132825-A1 Methods of treating cancer with HDAC inhibitors HDAC5, HDAC9, HDAC1 HDAC4 4/4885HDAC1 3/4885HDAC7 7/4885
US-20070060614-A1 Methods of treating cancer with hdac inhibitors HDAC5, BCL6, HDAC9 HDAC4 4/4885HDAC1 5/4885HDAC7 9/4885
US-11298363-B2 Triazolobenzazepines as vasopressin V1a receptor antagonists AVPR1B, AVPR1A, AVPR2 HDAC4 1236/4885HDAC1 602/4885HDAC7 1863/4885
US-20260125343-A1 METHODS FOR PREPARING HIGH-PURITY VORINOSTAT AND PRECURSORS THEREOF HDAC8, HDAC7, SUB1 HDAC4 7/4885HDAC1 4/4885HDAC7 2/4885
US-11046715-B2 Boronic derivatives of hydroxamates as anticancer agents BCOR, BRDT, HDAC1 HDAC4 15/4885HDAC1 3/4885HDAC7 16/4885

“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.