SCHEMBL13754465

SCHEMBL13754465

[N-]=[N+]=NCc1ccc(F)cc1

nearest known ligand 0.47

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ MIF P14174 1/20 0.47
▸ PPARG P37231 1/20 0.43
▸ IDO1 P14902 3/20 0.41
▸ LOXL2 Q9Y4K0 1/20 0.41
▸ HDAC3 O15379 1/20 0.40
▸ HDAC1 Q13547 1/20 0.40
▸ HDAC2 Q92769 1/20 0.40
▸ HDAC8 Q9BY41 1/20 0.40
▸ HDAC6 Q9UBN7 1/20 0.40
▸ TAAR1 Q96RJ0 3/20 0.38
▸ AGXT P21549 2/20 0.37
▸ ACHE P22303 1/20 0.35
▸ C3AR1 Q16581 1/20 0.34
▸ PLA2G1B P04054 1/20 0.33
▸ ATG4B Q9Y4P1 1/20 0.33
▸ MAOB P27338 1/20 0.33
▸ CTBP2 P56545 1/20 0.33

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
SCHEMBL17070603 1.00 MIF (0.47) MIFPPARGIDO1LOXL2HDAC3
SCHEMBL14189703 0.88 HDAC3 (0.45) PPARGHDAC3HDAC1HDAC2HDAC8
SCHEMBL15590852 0.81 HDAC3 (0.41) PPARGHDAC3HDAC1HDAC2HDAC8
SCHEMBL15590854 0.81 HDAC3 (0.41) PPARGHDAC3HDAC1HDAC2HDAC8
SCHEMBL15233019 0.81 HDAC1 (0.41) PPARGHDAC3HDAC1HDAC2HDAC8
SCHEMBL14270135 0.80 TAAR1 (0.46) MIFIDO1LOXL2TAAR1AGXT
SCHEMBL14280518 0.79 HDAC3 (0.44) IDO1HDAC3HDAC1HDAC2HDAC8
SCHEMBL14192686 0.78 PPARG (0.42) PPARGHDAC3HDAC1HDAC2HDAC8
SCHEMBL13627738 0.77 HDAC3 (0.40) PPARGHDAC3HDAC1HDAC2HDAC8
SCHEMBL21348198 0.77 HDAC3 (0.40) PPARGHDAC3HDAC1HDAC2HDAC8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119528900-A Methylthiazole derivative with anti-liver cancer activity and preparation method and application thereof 河南科技大学 2025-02-28 — — CN claimed
CN-118994141-A Phenylthiazole derivative with anti-liver cancer and anti-inflammatory activities and preparation method and application thereof 河南科技大学 2024-11-22 — — CN claimed
CN-118994140-A Triazole derivative with antidepressant effect, and preparation method and application thereof 河南科技大学 2024-11-22 — — CN claimed
CN-115636817-A Isatin derivative containing triazole ring and preparation method and application thereof 山东大学 2023-01-24 — — CN claimed
CN-109705095-B Fused ring p-benzoquinone CDC25 protein phosphatase inhibitor containing triazole ring, and preparation method and application thereof 山东大学 2021-06-08 — — CN claimed
US-9309225-B2 N-((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)arylamide compounds as potential anticancer agents and a process for the preparation thereof COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2016-04-12 — — US claimed
US-20150166507-A1 N-((1-BENZYL-1H-1,2,3-TRIAZOL-4-YL)METHYL)ARYLAMIDE COMPOUNDS AS POTENTIAL ANTICANCER AGENTS AND A PROCESS FOR THE PREPARATION THEREOF COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2015-06-18 — — US claimed
CN-122059846-A Method for synthesizing benzyl azide by tubular reactor 山东弗鲁微科技有限公司 2026-05-19 — — CN disclosed
US-12473263-B2 Bicyclic inhibitors of CBX chromodomains ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (US) 2025-11-18 — — US disclosed
WO-2025229046-A1 SUBSTITUTED HYDROQUINOLINES FOR THE TREATMENT OF GLIOBLASTOMA MULTIFORME MOLIUS SAGLIK TEKNOLOJILERI ANONIM SIRKETI (TR) 2025-11-06 — — WO disclosed
EP-4644375-A1 SUBSTITUTED HYDROQUINOLINES FOR THE TREATMENT OF GLIOBLASTOMA MULTIFORME Molius Saglik Teknolojileri Anonim Sirketi (TR) 2025-11-05 — — EP disclosed
WO-2025104092-A1 MODULATORS OF SEPTIN 6 FOR USE IN THE PREVENTION AND/OR TREATMENT OF NEURODEGENERATIVE DISORDERS REMYND N.V. (BE) 2025-05-22 — — WO disclosed
WO-2025104081-A1 TRIAZOLE DERIVATIVES AND THEIR USE IN THE TREATMENT OF NEURODEGENERATIVE DISORDERS REMYND N.V. (BE) 2025-05-22 — — WO disclosed
US-8202843-B2 Macrocyclic compounds and methods of making and using the same RIB-X PHARMACEUTICALS, INC. (US) 2012-06-19 — — US disclosed
US-8202843-B2 Macrocyclic compounds and methods of making and using the same RIB-X PHARMACEUTICALS, INC. (US) 2012-06-19 — — US disclosed
US-20100029722-A1 ORGANIC COMPOUNDS NOVARTIS AG (CH) 2010-02-04 — — US disclosed
CN-101595105-A 5 membered heterocyclic compounds that replace as the 2-of SCD inhibitor NOVARTIS AG XENON PHARMACEUTIC (CH) 2009-12-02 — — CN disclosed
WO-2009105746-A2 TRIAZOLES AND PROCESSES FOR PRODUCING THE SAME UNIVERSITY OF SOUTH FLORIDA (US) 2009-08-27 — — WO disclosed
US-20080045585-A1 Macrocyclic Compounds And Methods Of Making And Using The Same BioVersys AG (CH) 2008-02-21 — — US disclosed
US-20080045585-A1 Macrocyclic Compounds And Methods Of Making And Using The Same BioVersys AG (CH) 2008-02-21 — — 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 (4 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-20150166507-A1 N-((1-BENZYL-1H-1,2,3-TRIAZOL-4-YL)METHYL)ARYLAMIDE COMPOUNDS AS POTENTIAL ANTICANCER AGENTS AND A PROCESS FOR THE PREPARATION THEREOF CRBN, MCL1, DOT1L MIF 4585/4885PPARG 4798/4885IDO1 1557/4885
US-12473263-B2 Bicyclic inhibitors of CBX chromodomains CBX2, CBX3, CBX6 MIF 4076/4885PPARG 2375/4885IDO1 892/4885
US-20080045585-A1 Macrocyclic Compounds And Methods Of Making And Using The Same VIP, PROKR1, PGC MIF 28/4885PPARG 842/4885IDO1 1174/4885
US-20100029722-A1 ORGANIC COMPOUNDS SCD, SCD5, FADS2 MIF 3763/4885PPARG 28/4885IDO1 1239/4885

“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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