SCHEMBL403583

SCHEMBL403583

CCCCCCCCCCCCCCCCCCNc1nc(NCCCCCCCCCCCCCCCCCC)nc(NCCCCCCCCCCCCCCCCCC)n1

nearest known ligand 0.67

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 1/20 0.67
KCNH3 Q9ULD8 2/20 0.61
DNM2 P50570 9/20 0.56
SLC29A1 Q99808 1/20 0.48
MAPT P10636 1/20 0.48
HTT P42858 1/20 0.48
NPSR1 Q6W5P4 1/20 0.48
EPHX1 P07099 1/20 0.46
CA1 P00915 1/20 0.45
CA2 P00918 1/20 0.45
CA9 Q16790 1/20 0.45
CYP1A2 P05177 1/20 0.44
CYP2C19 P33261 1/20 0.44

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
SCHEMBL3299537 1.00 KMT2A (0.67) KMT2AKCNH3DNM2SLC29A1MAPT
SCHEMBL3298608 1.00 KMT2A (0.67) KMT2AKCNH3DNM2SLC29A1MAPT
SCHEMBL14441519 1.00 KMT2A (0.67) KMT2AKCNH3DNM2SLC29A1MAPT
SCHEMBL8054465 1.00 KMT2A (0.67) KMT2AKCNH3DNM2SLC29A1MAPT
SCHEMBL3298621 1.00 KMT2A (0.67) KMT2AKCNH3DNM2SLC29A1MAPT
SCHEMBL14441528 1.00 KMT2A (0.67) KMT2AKCNH3DNM2SLC29A1MAPT
SCHEMBL1032562 1.00 KMT2A (0.67) KMT2AKCNH3DNM2SLC29A1MAPT
SCHEMBL7774845 0.98 KMT2A (0.65) KMT2AKCNH3DNM2SLC29A1MAPT
SCHEMBL7776218 0.98 KMT2A (0.65) KMT2AKCNH3DNM2SLC29A1MAPT
SCHEMBL2783126 0.98 KMT2A (0.65) KMT2AKCNH3DNM2SLC29A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026088005-A1 PERSONAL PROTECTIVE EQUIPMENT, METHODS AND SYSTEMS OF USE THEREOF 3M INNOVATIVE PROPERTIES COMPANY (US) 2026-04-30 WO disclosed
EP-4694984-A1 RESPIRATORY PROTECTION DEVICES AND METHODS OF MANUFACTURING THE SAME 3M Innovative Properties Company (US) 2026-02-18 EP disclosed
EP-4694999-A1 FILTER MEDIA FOR FILTRATION DEVICES AND METHODS OF MAKING AND USING THE SAME 3M Innovative Properties Company (US) 2026-02-18 EP disclosed
US-12552914-B2 Substituted thiolate salt melt additives 3M INNOVATIVE PROPERTIES COMPANY (US) 2026-02-17 US disclosed
US-12467174-B2 Substituted benzimidazole melt additives 3M INNOVATIVE PROPERTIES COMPANY (US) 2025-11-11 US disclosed
EP-4637956-A1 SHIRRED FILTER MEDIA AND METHODS OF MAKING AND USING THE SAME 3M Innovative Properties Company (US) 2025-10-29 EP disclosed
US-12420223-B2 Composite non-woven fabric and article comprising same TORAY ADVANCED MATERIALS KOREA INC. (KR) 2025-09-23 US disclosed
US-12415150-B2 Composite nonwoven fabric and article comprising same TORAY ADVANCED MATERIALS KOREA INC. (KR) 2025-09-16 US disclosed
US-12409401-B2 Pleated filtration assembly comprising spunbonded prefilter 3M INNOVATIVE PROPERTIES COMPANY (US) 2025-09-09 US disclosed
EP-4069899-B1 AROMATIC-HETEROCYCLIC RING MELT ADDITIVES 3M INNOVATIVE PROPERTIES COMPANY (US) 2025-08-13 EP disclosed
EP-0565774-B1 Process for preparing amide derivatives from halominotriazines and acid halides CYTEC TECH CORP (US) 2001-03-28 EP disclosed
EP-0933369-A1 Tris-(omega-haloacyl)melamines CYTEC TECHNOLOGY CORP. (US) 1999-08-04 EP disclosed
EP-0933370-A1 Tris-(2,2,6,6-tetramethyl-piperid-4-yl-aminocarbonyl)melamine CYTEC TECHNOLOGY CORP. (US) 1999-08-04 EP disclosed
EP-0933371-A1 N-halo acid amides CYTEC TECHNOLOGY CORP. (US) 1999-08-04 EP disclosed
EP-0930303-A2 A process for preparing isocyanate compounds from haloaminotriazines and acid halides CYTEC TECHNOLOGY CORP. (US) 1999-07-21 EP disclosed
US-5571915-A Process for preparing amide derivatives from haloaminotriazines and acid halides CYTEC TECHNOLOGY CORP. (US) 1996-11-05 US disclosed
US-5405959-A Haloaminotraizines and acid halides CYTEC TECHNOLOGY CORP. (US) 1995-04-11 US disclosed
US-5288865-A Process for preparing amide derivatives from haloaminotriazines and acid halides AMERICAN CYANAMID COMPANY (US) 1994-02-22 US disclosed
EP-0565774-A2 Process for preparing amide derivatives from halominotriazines and acid halides CYTEC TECHNOLOGY CORP. (US) 1993-10-20 EP disclosed
EP-0541966-A2 Process for preparing amide derivatives from halomines and acid halides AMERICAN CYANAMID COMPANY (US) 1993-05-19 EP 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 (2 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-12552914-B2 Substituted thiolate salt melt additives FRG1, EXOSC4, SCNN1G KMT2A 1772/4885KCNH3 1231/4885DNM2 2863/4885
US-12467174-B2 Substituted benzimidazole melt additives SMARCA4, BRD4, ARID2 KMT2A 341/4885KCNH3 2331/4885DNM2 1866/4885

“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.