SCHEMBL62779

SCHEMBL62779

CNC(=O)c1cccc(C=O)c1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
UNG P13051 1/20 0.61
HDAC8 Q9BY41 3/20 0.59
HDAC6 Q9UBN7 3/20 0.59
SLC7A5 Q01650 1/20 0.49
HDAC3 O15379 1/20 0.46
HDAC1 Q13547 1/20 0.46
RAF1 P04049 2/20 0.46
TRIM24 O15164 1/20 0.45
TRIM33 Q9UPN9 1/20 0.45
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
KDM4E B2RXH2 2/20 0.43
CHEK1 O14757 1/20 0.43
NPC1 O15118 1/20 0.43
RAB9A P51151 1/20 0.43
ALDH1A1 P00352 2/20 0.42
HDAC2 Q92769 1/20 0.42
SRC P12931 1/20 0.42
POLB P06746 1/20 0.42
NAT1 P18440 1/20 0.42

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
SCHEMBL29957694 1.00 UNG (0.61) UNGHDAC8HDAC6SLC7A5HDAC3
SCHEMBL15650707 0.88 NPC1 (0.53) UNGHDAC8HDAC6MEN1KMT2A
SCHEMBL24527569 0.84 HDAC8 (0.58) UNGHDAC8HDAC6SLC7A5HDAC3
SCHEMBL27210087 0.83 HDAC1 (0.65) UNGHDAC8HDAC6HDAC3HDAC1
SCHEMBL5909363 0.82 HDAC8 (0.83) HDAC8HDAC6SLC7A5MEN1KMT2A
SCHEMBL12651049 0.82 CRBN (0.54) HDAC8HDAC6TRIM24TRIM33MEN1
SCHEMBL9655260 0.81 UNG (0.61) UNGHDAC3HDAC1TRIM24TRIM33
SCHEMBL8129512 0.81 HDAC8 (0.54) HDAC8HDAC6SLC7A5HDAC3HDAC1
SCHEMBL6184692 0.81 UNG (0.56) UNGHDAC3HDAC1MEN1KMT2A
SCHEMBL15652250 0.81 ERN1 (0.58) UNGHDAC3HDAC1KMT2AKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4626427-A1 COMBINATIONS COMPRISING A MENIN-MLL INHIBITOR AND A BCL-2 INHIBITOR Janssen Pharmaceutica NV (BE) 2025-10-08 EP disclosed
EP-4626426-A1 COMBINATIONS COMPRISING A MENIN-MLL INHIBITOR AND AT LEAST ONE OTHER THERAPEUTIC AGENT JANSSEN Pharmaceutica NV (BE) 2025-10-08 EP disclosed
CN-115260165-B Benzo nitrogen-containing five-membered heterocyclic compound and synthesis and application thereof 中国科学院上海药物研究所 2024-08-06 CN disclosed
WO-2024114664-A1 COMBINATIONS COMPRISING A MENIN-MLL INHIBITOR AND AT LEAST ONE OTHER THERAPEUTIC AGENT JANSSEN PHARMACEUTICA NV (BE) 2024-06-06 WO disclosed
WO-2024114666-A1 COMBINATIONS COMPRISING A MENIN-MLL INHIBITOR AND A BCL-2 INHIBITOR JANSSEN PHARMACEUTICA NV (BE) 2024-06-06 WO disclosed
US-20240139125-A1 BI-1 ANTAGONISTS AND THEIR USES INDUSTRIAL COOPERATION FOUNDATION JEONBUK NATIONAL UNIVERSITY (KR) 2024-05-02 US disclosed
EP-4347588-A1 SUBSTITUTED PHENYL-1H-PYRROLO[2, 3-C]PYRIDINE DERIVATIVES JANSSEN Pharmaceutica NV (BE) 2024-04-10 EP disclosed
US-11932639-B2 Fused ring heteroaryl compounds as ALK4/5 inhibitors BISICHEM CO., LTD. (KR) 2024-03-19 US disclosed
CN-117396476-A Substituted phenyl-1H-pyrrolo [2,3-c ] pyridine derivatives 詹森药业有限公司 2024-01-12 CN disclosed
WO-2023154344-A1 2-METHYL-4',5'-DIHYDROSPIRO[PIPERIDINE-4,7'-THIENO[2,3-C]PYRAN] DERIVATIVES AS INHIBITORS OF APOL1 AND METHODS OF USING SAME VERTEX PHARMACEUTICALS INCORPORATED (US) 2023-08-17 WO disclosed
US-20060122209-A1 Process for preparing trisubstituted pyrimidine compounds SYNTA PHARMACEUTICALS CORP. (US) 2006-06-08 US disclosed
WO-2006053112-A1 PROCESS FOR PREPARING TRISUBSTITUTED PYRIMIDINE COMPOUNDS SYNTA PHARMACEUTICALS CORP. (US) 2006-05-18 WO disclosed
US-20040248947-A1 Anthranilic acid amides and pharmaceutical use thereof NOVARTIS AG (CH) 2004-12-09 US disclosed
US-6624174-B2 Especially for treating a neoplastic disease, retinopathy or age-related macular degeneration NOVARTIS AG (CH) 2003-09-23 US disclosed
US-20030032656-A1 2-Amino-nicotinamide derivatives and their use as vegf-receptor tyrosine kinase inhibitors NOVARTIS AG (CH) 2003-02-13 US disclosed
EP-0819129-B1 PYRAZOLE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF NOVARTIS AG (CH) 2000-08-02 EP disclosed
US-5981533-A INHIBIT THE TYROSINE KINASE ACTIVITY OF THE RECEPTOR FOR EPIDERMAL GROWTH FACTOR AND CAN BE USED IN THE CASE OF EPIDERMAL HYPERPROLIFERATION (PSORIASIS) AND AS ANTI-TUMOR AGENTS NOVARTIS AG (CH) 1999-11-09 US disclosed
WO-1998014449-A1 FUSED PYRAZOLE DERIVATIVES AND PROCESSES FOR THEIR PREPARATION NOVARTIS AG (CH) 1998-04-09 WO disclosed
EP-0819129-A1 PYRAZOLE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF Novartis AG (CH) 1998-01-21 EP disclosed
WO-1996031510-A1 PYRAZOLE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF NOVARTIS AG (CH) 1996-10-10 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 (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-20060122209-A1 Process for preparing trisubstituted pyrimidine compounds TYMS, NUDT1, TYMP UNG 47/4885HDAC8 3180/4885HDAC6 2180/4885
US-20040248947-A1 Anthranilic acid amides and pharmaceutical use thereof AFF1, FFAR1, FFAR2 UNG 4604/4885HDAC8 739/4885HDAC6 1630/4885
US-11932639-B2 Fused ring heteroaryl compounds as ALK4/5 inhibitors ALK, FGFR4, ALKBH3 UNG 1416/4885HDAC8 1877/4885HDAC6 2078/4885
US-20030032656-A1 2-Amino-nicotinamide derivatives and their use as vegf-receptor tyrosine kinase inhibitors KDR, ERBB2, FLT1 UNG 2819/4885HDAC8 2023/4885HDAC6 1038/4885
US-20240139125-A1 BI-1 ANTAGONISTS AND THEIR USES TMBIM6, RPS6KB1, RACK1 UNG 3700/4885HDAC8 1854/4885HDAC6 1865/4885

“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.