SCHEMBL3758635

SCHEMBL3758635

Nc1ccc(-n2cc(-c3ccccc3)nn2)cc1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 7/20 0.66
CA1 P00915 6/20 0.66
CA9 Q16790 5/20 0.66
PTGS2 P35354 4/20 0.66
CA5A P35218 4/20 0.66
CA5B Q9Y2D0 4/20 0.66
CA12 O43570 4/20 0.66
PTGS1 P23219 1/20 0.61
OGT O15294 2/20 0.55
BCHE P06276 1/20 0.53
HSD17B1 P14061 1/20 0.53
HSD17B2 P37059 1/20 0.53
FLT3 P36888 2/20 0.51
GSK3B P49841 1/20 0.51
MIF P14174 1/20 0.50
KEAP1 Q14145 1/20 0.50
NFE2L2 Q16236 1/20 0.50
CYP19A1 P11511 1/20 0.50
HDAC3 O15379 1/20 0.48
HDAC1 Q13547 1/20 0.48

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
SCHEMBL11904306 0.93 CA1 (0.57) CA2CA1CA9PTGS2CA5A
SCHEMBL21122002 0.88 HSD17B1 (0.63) CA2CA1CA9PTGS2CA5A
SCHEMBL26628312 0.87 PTGS2 (0.67) CA2CA1CA9PTGS2CA5A
SCHEMBL1119554 0.87 PTGS2 (0.66) CA2CA1CA9PTGS2CA5A
SCHEMBL23999844 0.87 OGT (0.56) CA2CA1CA9PTGS2CA5A
Bromide SCHEMBL6256547 0.85 PTGS2 (0.64) CA2CA1CA9PTGS2CA5A
SCHEMBL28949786 0.83 HSD17B1 (0.61) CA2CA1CA9PTGS2CA5A
SCHEMBL12599087 0.83 HSD17B1 (0.74) CA2CA1CA9PTGS2CA5A
SCHEMBL12522541 0.83 FLT3 (0.73) CA2CA1CA9PTGS2CA5A
SCHEMBL12450544 0.83 CA2 (0.61) CA2CA1CA9PTGS2CA5A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20180182566-A1 METHOD FOR PREPARING A COMPOSITE ELECTRODE CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2018-06-28 US disclosed
CN-103113315-B The 1H-1 that 1-aryl replaces, the preparation method of 2,3-triazole class compounds JIANG University OF TECHNOLOGY (CN) 2016-01-20 CN disclosed
US-20150232429-A1 SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS THE SCRIPPS RESEARCH INSTITUTE 2015-08-20 US disclosed
US-9018205-B2 Substituted pyrimidinyl-amines as protein kinase inhibitors THE SCRIPPS RESEARCH INSTITUTE (US) 2015-04-28 US disclosed
EP-2200436-B1 SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS SCRIPPS RESEARCH INST (US) 2015-01-21 EP disclosed
US-8530480-B2 Substituted pyrimidinyl-amines as protein kinase inhibitors THE SCRIPPS RESEARCH INSTITUTE (US) 2013-09-10 US disclosed
US-20130231336-A1 SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS THE SCRIPPS RESEARCH INSTITUTE (US) 2013-09-05 US disclosed
CN-103113315-A Preparation method of 1-aryl substituted 1H-1, 2, 3-triazole compound UNIV ZHEJIANG TECHNOLOGY 2013-05-22 CN disclosed
US-20100298312-A1 SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS THE SCRIPPS RESEARCH INSTITUTE (US) 2010-11-25 US disclosed
EP-2200436-A1 SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS The Scripps Research Institute (US) 2010-06-30 EP disclosed
WO-2009032861-A1 SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS THE SCRIPPS RESEARCH INSTITUTE (US) 2009-03-12 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 (3 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-20130231336-A1 SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS MAP3K20, MAP3K5, MAP3K7 CA2 4772/4885CA1 4875/4885CA9 4874/4885
US-20100298312-A1 SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS MAP3K20, MAP3K5, MAP3K7 CA2 4772/4885CA1 4875/4885CA9 4874/4885
US-20150232429-A1 SUBSTITUTED PYRIMIDINYL-AMINES AS PROTEIN KINASE INHIBITORS MAP3K20, MAP3K5, MAP3K7 CA2 4772/4885CA1 4875/4885CA9 4874/4885

“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.