SCHEMBL912709

SCHEMBL912709

Cc1nc(Cl)nc(N2CCOCC2)n1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.54
L3MBTL1 Q9Y468 1/20 0.54
KMT2A Q03164 2/20 0.49
KDM4E B2RXH2 3/20 0.46
HTT P42858 3/20 0.46
ALDH1A1 P00352 2/20 0.45
HPGD P15428 1/20 0.45
SMN1; SMN2 Q16637 2/20 0.45
MAPK1 P28482 1/20 0.45
MEN1 O00255 1/20 0.44
TDP1 Q9NUW8 1/20 0.43
PIK3CA P42336 3/20 0.43
PIK3R1 P27986 2/20 0.43
MTOR P42345 2/20 0.43
NPSR1 Q6W5P4 3/20 0.43
HRH4 Q9H3N8 1/20 0.43
LMNA P02545 1/20 0.43
CYP1A2 P05177 1/20 0.43
CYP3A4 P08684 1/20 0.43
CYP2C9 P11712 1/20 0.43

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
SCHEMBL9619196 0.86 KDM4E (0.58) KMT2AKDM4EHTTALDH1A1HPGD
SCHEMBL38827 0.86 MAPT (0.57) MAPTL3MBTL1KMT2AKDM4EHTT
SCHEMBL12110268 0.86 KMT2A (0.56) MAPTKMT2AKDM4EHTTALDH1A1
SCHEMBL1308905 0.86 MAPT (0.61) MAPTL3MBTL1KMT2AKDM4EHTT
SCHEMBL22924660 0.82 HRH4 (0.47) MAPTL3MBTL1KMT2AHTTMAPK1
SCHEMBL20805760 0.82 MAPK1 (0.44) MAPTL3MBTL1KMT2AHTTALDH1A1
SCHEMBL2689185 0.81 KMT2A (0.49) MAPTL3MBTL1KMT2AKDM4EHTT
SCHEMBL28998051 0.81 ALDH1A1 (0.59) MAPTL3MBTL1KMT2AKDM4EHTT
SCHEMBL19295119 0.81 MAPK1 (0.47) L3MBTL1KMT2AHTTALDH1A1SMN1; SMN2
SCHEMBL1310780 0.80 MAPT (0.60) MAPTL3MBTL1KMT2AKDM4EHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230399302-A1 PROCESS FOR THE PREPARATION OF HETEROARYL-SUBSTITUTED SULFUR(VI) COMPOUNDS NATIONAL INSTITUTES OF HEALTH 2023-12-14 US disclosed
US-20230129089-A1 PREPARATION OF A 1,3,5-TRIAZINYL BENZIMIDAZOLE MEI PHARMA, INC. 2023-04-27 US disclosed
EP-2473486-B2 PYRIMIDINES AS HEPCIDINE ANTAGONISTS VIFOR INT AG (CH) 2021-09-22 EP disclosed
EP-2473486-B2 PYRIMIDINES AS HEPCIDINE ANTAGONISTS VIFOR INT AG (CH) 2021-09-22 EP disclosed
WO-2020058337-A1 USE OF A MELAMINE BASED COMPOUND AND A HALS COMPOUND AS HEAT STABILIZER IN POLYMERS BOREALIS AG (AT) 2020-03-26 WO disclosed
EP-3174890-B1 METAL COMPLEXES MERCK PATENT GMBH (DE) 2019-03-13 EP disclosed
US-9853228-B2 Metal complexes MERCK PATENT GMBH (DE) 2017-12-26 US disclosed
US-9853228-B2 Metal complexes MERCK PATENT GMBH (DE) 2017-12-26 US disclosed
WO-2017198346-A1 TREATMENT OF NEUROLOGICAL DISORDERS PIQUR THERAPEUTICS AG (CH) 2017-11-23 WO disclosed
US-20170250353-A1 METAL COMPLEXES MERCK PATENT GMBH (DE) 2017-08-31 US disclosed
US-20070113356-A1 Reactive polysaccharide derivatives, their preparation and their use CIBA SPECIALTY CHEMICALS CORP. (US) 2007-05-24 US disclosed
US-20070113356-A1 Reactive polysaccharide derivatives, their preparation and their use CIBA SPECIALTY CHEMICALS CORP. (US) 2007-05-24 US disclosed
EP-1765325-A2 2-SUBSTITUTED HETEROARYL COMPOUNDS Synta Pharmaceuticals Corporation (US) 2007-03-28 EP disclosed
US-7169835-B2 Stabilizer mixture CIBA SPECIALTY CHEMICALS CORPORATION (US) 2007-01-30 US disclosed
US-20060063739-A1 2-Substituted heteroaryl compounds LSI FINANCING LLC, AS ADMINISTRATIVE AGENT 2006-03-23 US disclosed
WO-2006007532-A2 2-SUBSTITUTED HETEROARYL COMPOUNDS SYNTA PHARMACEUTICALS CORP. (US) 2006-01-19 WO disclosed
US-6342503-B1 ANTIDEPRESSANTS, EATING DISORDERS DUPONT PHARMACEUTICALS COMPANY 2002-01-29 US disclosed
US-6107301-A PSYCHOLOGICAL DISORDERS DUPONT PHARMACEUTICALS COMPANY (US) 2000-08-22 US disclosed
EP-0723533-A1 1N-ALKYL-N-ARYLPYRIMIDINAMINES AND DERIVATIVES THEREOF THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1996-07-31 EP disclosed
WO-1995010506-A1 1N-ALKYL-N-ARYLPYRIMIDINAMINES AND DERIVATIVES THEREOF THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1995-04-20 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-20230129089-A1 PREPARATION OF A 1,3,5-TRIAZINYL BENZIMIDAZOLE CYP2E1, CYP3A4, PAICS MAPT 2578/4885L3MBTL1 2936/4885KMT2A 1897/4885
US-20070113356-A1 Reactive polysaccharide derivatives, their preparation and their use C1S, H1-0, H1-4 MAPT 4550/4885L3MBTL1 2580/4885KMT2A 2501/4885
US-20230399302-A1 PROCESS FOR THE PREPARATION OF HETEROARYL-SUBSTITUTED SULFUR(VI) COMPOUNDS TST, TYR, STS MAPT 3431/4885L3MBTL1 3794/4885KMT2A 1707/4885
US-20170250353-A1 METAL COMPLEXES SOD1, AP1M1, AP3M1 MAPT 1084/4885L3MBTL1 3160/4885KMT2A 2922/4885
US-20060063739-A1 2-Substituted heteroaryl compounds IL2, IL4, IL2RA MAPT 1171/4885L3MBTL1 4762/4885KMT2A 3580/4885

“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.