SCHEMBL13649287

SCHEMBL13649287

[N-]=[N+]=Nc1ccncc1

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL28674817 0.86 ALOX5 (0.52) —
SCHEMBL13475898 0.81 CYP51A1 (0.45) —
SCHEMBL16748959 0.80 CA1 (0.58) —
Benzene SCHEMBL28456073 0.72 PTGS2 (0.48) —
SCHEMBL13475909 0.72 — —
SCHEMBL13667405 0.72 CA1 (0.52) —
SCHEMBL15845029 0.72 CA1 (0.52) —
SCHEMBL13667432 0.72 CA1 (0.52) —
SCHEMBL13464080 0.72 — —
SCHEMBL30184791 0.72 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117801053-A Cell membrane protein enrichment method based on phospholipase enzymatic markers 福建医科大学 2024-04-02 — — CN claimed
US-5277772-A Generating a reactive intermediate E. I. DU PONT DE NEMOURS AND COMPANY (US) 1994-01-11 — — US claimed
US-20260035341-A1 FTO INHIBITORS RPXDS CO LTD (CN) 2026-02-05 — — US disclosed
EP-4561975-A1 FTO INHIBITORS RPXDS Co., Ltd (CN) 2025-06-04 — — EP disclosed
CN-120058675-A Preparation and purification method and application of quinoline derivative with biological activity 河南科技大学 2025-05-30 — — CN disclosed
US-20250134890-A1 ANTIMALARIAL HEXAHYDROPYRIMIDINE ANALOGUES UCB Biopharma SRL (BE) 2025-05-01 — — US disclosed
CN-119546566-A FTO inhibitors 瑞璞鑫(苏州)生物科技有限公司 2025-02-28 — — CN disclosed
CN-113874423-B Compositions, methods and systems for forming beads using improved polymers 10X基因组学有限公司 2025-02-14 — — CN disclosed
CN-107922387-B Heterocyclic inhibitors of ERK1 and ERK2 and their use in cancer treatment 阿沙纳生物科学公司 2024-11-22 — — CN disclosed
CN-117801053-A Cell membrane protein enrichment method based on phospholipase enzymatic markers 福建医科大学 2024-04-02 — — CN disclosed
US-11925629-B2 Heterocyclic inhibitors of ERK1 and ERK2 and their use in the treatment of cancer ASANA BIOSCIENCES, LLC (US) 2024-03-12 — — US disclosed
US-20090118503-A1 FAAH INHIBITORS IRONWOOD PHARMACEUTICALS, INC. 2009-05-07 — — US disclosed
US-20090118503-A1 FAAH INHIBITORS IRONWOOD PHARMACEUTICALS, INC. 2009-05-07 — — US disclosed
WO-2008157740-A2 FAAH INHIBITORS IRONWOOD PHARMACEUTICALS, INC. (US) 2008-12-24 — — 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
US-20070191389-A1 Biaryl derivatives BANYU PHARMACEUTICAL CO., LTD. (JP) 2007-08-16 — — US disclosed
CN-1980901-A Biaryl derivatives BANYU PHARMA CO LTD (JP) 2007-06-13 — — CN disclosed
EP-1764362-A1 BIARYL DERIVATIVES BANYU PHARMACEUTICAL CO., LTD. (JP) 2007-03-21 — — EP disclosed
US-5277772-A Generating a reactive intermediate E. I. DU PONT DE NEMOURS AND COMPANY (US) 1994-01-11 — — US disclosed
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