SCHEMBL5134210

SCHEMBL5134210

Nc1nnnc2nn[nH]c12

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
SCHEMBL462247 0.70 PDPK1 (0.45) —
SCHEMBL31561489 0.70 PDPK1 (0.45) —
SCHEMBL6153817 0.68 — —
SCHEMBL2115830 0.64 PI4KA (0.55) —
SCHEMBL210649 0.57 — —
SCHEMBL31561553 0.54 CHEK1 (0.41) —
SCHEMBL3790626 0.53 — —
SCHEMBL5933484 0.53 — —
Boric Acid SCHEMBL8816913 0.49 — —
SCHEMBL6049955 0.49 CASP1 (0.33) —

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4685144-A1 NON-FLUORESCENT COMPOUND AND USES THEREOF SFC Co., Ltd. (KR) 2026-01-28 — — EP disclosed
US-20260015655-A1 COMPOUNDS AND THEIR APPLICATIONS SFC CO., LTD. (KR) 2026-01-15 — — US disclosed
EP-4674845-A1 NOVEL COMPOUND AND USE THEREOF SFC Co., Ltd. (KR) 2026-01-07 — — EP disclosed
WO-2024228496-A1 NON-FLUORESCENT COMPOUND AND USES THEREOF 에스에프씨 주식회사 2024-11-07 — — WO disclosed
WO-2024225787-A1 NOVEL COMPOUND AND USE THEREOF 에스에프씨 주식회사 2024-10-31 — — WO disclosed
US-9012182-B2 Method for producing purine nucleosides and nucleotides by fermentation using bacterium belonging to the genus Bacillus or Escherichia AJINOMOTO CO., INC. (JP) 2015-04-21 — — US disclosed
CN-101120090-B Process for producing purine nucleosides and nucleotides by fermentation using bacteria belonging to the genus Bacillus or Escherichia AJINOMOTO KK 2012-05-23 — — CN disclosed
US-20080241888-A1 Transgenic microorganism with enhanced expression of metabolic efflux pumps for use as bioreactor in biosynthesis of inosinic, xanthylic and guanylic acids AJINOMOTO CO., INC. (JP) 2008-10-02 — — US disclosed
CN-101120090-A Method for producing purine nucleosides and nucleotides by fermentation using bacterium belonging to the genus bacillus or escherichia AJINOMOTO KK (JP) 2008-02-06 — — CN disclosed
US-6919453-B1 Colorant compositions THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY (US) 2005-07-19 — — US disclosed
US-6673924-B2 EXPLOSIVES; PYROTECHNICS; CYCLIZATION OF DICYANDIAMIDE WITH HYDRAZINE HYDROCHLORIDE THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY 2004-01-06 — — US disclosed
US-6632305-B2 Chemical intermediates for use in explosives/pyrotechnics, herbicides, pesticides, fungicides and fertilizers THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE NAVY 2003-10-14 — — US disclosed
US-20030069247-A1 1,2,4-triazolo[4,3-a][1,3,5]triazine-3,5,7-substituted precursor, and process, and compounds therefrom NAVY, UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE SECRETARY 2003-04-10 — — US disclosed
US-20030013878-A1 1,2,4-triazolo[4,3-a][1,3,5]triazine-3,5,7-substituted precursor, and process, and compounds therefrom NAVY, UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE SECRETARY OF 2003-01-16 — — US disclosed
WO-2002098855-A2 1,2,4-TRIAZOLO[4,3-a][1,3,5]TRIAZINE-3,5,7-SUBSTITUTED PRECURSOR, AND PROCESS, AND COMPOUNDS THEREFROM MCDONNELL THOMAS E (US) 2002-12-12 — — WO disclosed
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