SCHEMBL2343565

SCHEMBL2343565

N#CC(N)=NNc1cccc(Cl)c1

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 7/20 0.71
SMN1; SMN2 Q16637 4/20 0.71
KMT2A Q03164 4/20 0.71
MEN1 O00255 3/20 0.71
TDP1 Q9NUW8 2/20 0.71
CYP3A4 P08684 1/20 0.71
ALOX15 P16050 1/20 0.71
TSHR P16473 1/20 0.71
HSD17B10 Q99714 1/20 0.71
CISD1 Q9NZ45 1/20 0.71
GAA P10253 6/20 0.57
LMNA P02545 2/20 0.57
HTT P42858 1/20 0.57
RAPGEF3 O95398 6/20 0.50
RAPGEF4 Q8WZA2 2/20 0.50
GFER P55789 2/20 0.48
HTR3E A5X5Y0 2/20 0.47
HTR3B O95264 2/20 0.47
HTR3A P46098 2/20 0.47
HTR3D Q70Z44 2/20 0.47

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
Carbonyl Cyanide M-Chlorophenylhydrazone SCHEMBL379195 0.83 MAPT (1.00) MAPTSMN1; SMN2KMT2AMEN1TDP1
Carbonyl Cyanide M-Chlorophenylhydrazone SCHEMBL29353613 0.83 MAPT (1.00) MAPTSMN1; SMN2KMT2AMEN1TDP1
SCHEMBL12648701 0.81 MAPT (0.66) MAPTSMN1; SMN2KMT2AMEN1TDP1
SCHEMBL9865909 0.77 MAPT (0.76) MAPTSMN1; SMN2KMT2AMEN1TDP1
SCHEMBL9868037 0.77 MAPT (0.76) MAPTSMN1; SMN2KMT2AMEN1TDP1
SCHEMBL9867790 0.76 MAPT (0.70) MAPTSMN1; SMN2KMT2AMEN1TDP1
SCHEMBL3678595 0.76 MAPT (0.70) MAPTSMN1; SMN2KMT2AMEN1TDP1
SCHEMBL9868710 0.74 MAPT (0.67) MAPTSMN1; SMN2KMT2AMEN1TDP1
SCHEMBL9868712 0.74 MAPT (0.67) MAPTSMN1; SMN2KMT2AMEN1TDP1
Carbonyl Cyanide M-Chlorophenylhydrazone SCHEMBL28977410 0.73 MAPT (0.76) MAPTSMN1; SMN2KMT2AMEN1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12214000-B2 Human uterine cervical stem cell population and uses thereof GISTEM RESEARCH S.L. (ES) 2025-02-04 US disclosed
US-20210299184-A1 HUMAN UTERINE CERVICAL STEM CELL POPULATION AND USES THEREOF GISTEM RESEARCH S.L. (ES) 2021-09-30 US disclosed
US-20160000835-A1 HUMAN UTERINE CERVICAL STEM CELL POPULATION AND USES THEREOF GISTEM RESEARCH S.L. (ES) 2016-01-07 US disclosed
WO-2014128291-A1 HUMAN UTERINE CERVICAL STEM CELL POPULATION AND USES THEREOF FUNDACION PARA LA INVESTIGACION CON CELULAS MADRE UTERINAS (ES) 2014-08-28 WO disclosed
EP-1553948-B1 COMBINATION OF IMATNIB AND A HISTONE DEACETYLASE INHIBITOR FOR THE TREATMENT OF LEUKEMIA UNIV VIRGINIA COMMONWEALTH (US) 2011-08-24 EP disclosed
US-7642051-B2 Induction of mitochondrial membrane permeabilization via the physical and functional interaction of the HIV-1 Vpr protein with the mitochondrial inner membrane protein ANT (also called adenine nucleotide translocase or ADP/ATP carrier) INSTITUT PASTEUR (FR) 2010-01-05 US disclosed
US-20090264439-A1 Combination of a) N--4-(3-pyridyl)-2-pyrimidine-amine and b) a histone deacetylase inhibitor for the treatment of leukemia DENT PAUL 2009-10-22 US disclosed
EP-1370572-B1 MITOCHONDRIAL MEMBRANE PERMEABILIZATION BY HIV-1 VPR AND METHODS OF SCREENING PASTEUR INSTITUT (FR) 2008-11-26 EP disclosed
US-7056735-B2 Mimetics and inhibitors of the interaction between Vpr (HIV viral protein of regulation) and ANT (Mitochondrial adenine nucleotide translocator) INSTITUT PASTEUR (FR) 2006-06-06 US disclosed
US-20060100140-A1 Combination of a) n-{5-[4-(4-methyl-piperazino-methyl)-benzoylamido]2-methylphenyl}-4- (3-pyridyl)-2-pyrimidine-amine and b) a histone deacetylase inhibitor for the treatment of leukemia NOVARTIS AG (CH) 2006-05-11 US disclosed
US-20060052285-A1 Mechanism of mitochondrial membrane permeabilization by HIV-1 VPR, mimetics of Vpr and methods of screening active molecules having the ability to alter and/or prevent and/or mimic the interaction of Vpr with ANT INSTITUT PASTEUR (FR) 2006-03-09 US disclosed
US-20040072146-A1 Mechanism of mitochondrial membrane permeabilization by HIV-1 Vpr, mimetics of Vpr and methods of screening active molecules having the ability to alter and/or prevent and/or mimic the interaction of Vpr with ANT UNIVERSITE DE TECHNOLOGIE DE COMPIEGNE (FR) 2004-04-15 US disclosed
US-20020068273-A1 Mimetics and inhibitors of the interaction between Vpr (HIV vIral protein of regulation) and ANT (mitochondrial adenine nucleotide translocator) INSTITUT PASTEUR (FR) 2002-06-06 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 (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-20090264439-A1 Combination of a) N--4-(3-pyridyl)-2-pyrimidine-amine and b) a histone deacetylase inhibitor for the treatment of leukemia HDAC5, HDAC2, HDAC1 MAPT 3984/4885SMN1; SMN2 2046/4885KMT2A 18/4885
US-20060100140-A1 Combination of a) n-{5-[4-(4-methyl-piperazino-methyl)-benzoylamido]2-methylphenyl}-4- (3-pyridyl)-2-pyrimidine-amine and b) a histone deacetylase inhibitor for the treatment of leukemia HDAC5, HDAC2, HDAC1 MAPT 4021/4885SMN1; SMN2 2118/4885KMT2A 18/4885

“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.