SCHEMBL4040925

SCHEMBL4040925

COc1ccc(Nc2[nH]nc3c2Cc2c(C)cccc2-3)c(OC)c1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.46
TP53 P04637 1/20 0.45
STK10 O94804 1/20 0.40
SLK Q9H2G2 1/20 0.40
MAPT P10636 3/20 0.39
NPC1 O15118 2/20 0.39
RAB9A P51151 2/20 0.39
SMN1; SMN2 Q16637 2/20 0.39
CRHBP P24387 1/20 0.39
CRHR2 Q13324 1/20 0.39
EIF2AK1 Q9BQI3 1/20 0.39
MEN1 O00255 3/20 0.39
GAA P10253 1/20 0.39
ALDH1A1 P00352 2/20 0.38
CCNA2 P20248 1/20 0.38
CDK2 P24941 1/20 0.38
TTK P33981 1/20 0.38
CYP1A2 P05177 1/20 0.38
CYP3A4 P08684 1/20 0.38
CYP2C9 P11712 1/20 0.38

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
SCHEMBL4044173 0.92 KMT2A (0.41) KMT2ATP53MAPTNPC1SMN1; SMN2
SCHEMBL4047572 0.91 TP53 (0.46) KMT2ATP53STK10SLKMAPT
SCHEMBL13145999 0.83 PDGFRB (0.44) KMT2ATP53MAPTNPC1SMN1; SMN2
SCHEMBL4045624 0.82 PDGFRB (0.47) KMT2ATP53MAPTNPC1RAB9A
SCHEMBL4042479 0.81 CHEK1 (0.51) PDGFRB
SCHEMBL4044383 0.77 PDGFRB (0.52) KMT2ASTK10SLKMAPTNPC1
SCHEMBL4048672 0.76 HIF1A (0.47) KMT2ATP53MAPTNPC1SMN1; SMN2
SCHEMBL4046765 0.76 NPC1 (0.36) KMT2ATP53MAPTNPC1RAB9A
SCHEMBL4051009 0.74 ACHE (0.44) MAPTRAB9ASMN1; SMN2ALDH1A1CYP1A2
SCHEMBL4044923 0.74 STK10 (0.43) KMT2ATP53STK10SLKMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7795440-B2 N-substituted tricyclic 1-aminopyrazoles as inhibitors for the treatment of cell proliferative disorders JANSSEN PHARMACEUTICA NV (BE) 2010-09-14 US disclosed
US-7795440-B2 N-substituted tricyclic 1-aminopyrazoles as inhibitors for the treatment of cell proliferative disorders JANSSEN PHARMACEUTICA NV (BE) 2010-09-14 US disclosed
EP-1506175-B1 N-SUBSTITUTED TRICYCLIC 3-AMINOPYRAZOLES AS PDGF RECEPTOR INHIBITORS JANSSEN PHARMACEUTICA NV (BE) 2009-04-01 EP disclosed
WO-2009024592-A1 PROCESSING OF LITHOGRAPHIC PRINTING PLATES WITH A DEVELOPER SOLUTION CONTAINING A HYDROPHILIC POLYMER EASTMAN KODAK COMPANY (US) 2009-02-26 WO disclosed
US-20070142305-A1 N-substituted tricyclic 1-aminopyrazoles as inhibitors for the treatment of cell proliferative disorders HO CHIH Y 2007-06-21 US disclosed
US-20070142305-A1 N-substituted tricyclic 1-aminopyrazoles as inhibitors for the treatment of cell proliferative disorders HO CHIH Y 2007-06-21 US disclosed
US-7196110-B2 N-substituted tricyclic 3-aminopyrazoles as inhibitors for the treatment of cell proliferative disorders JANSSEN PHAMACEUTICA N.V. (BE) 2007-03-27 US disclosed
US-7196110-B2 N-substituted tricyclic 3-aminopyrazoles as inhibitors for the treatment of cell proliferative disorders JANSSEN PHAMACEUTICA N.V. (BE) 2007-03-27 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 (1 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-20070142305-A1 N-substituted tricyclic 1-aminopyrazoles as inhibitors for the treatment of cell proliferative disorders PDGFRA, PDGFRB, PDGFA KMT2A 2557/4885TP53 109/4885STK10 1239/4885

“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.