SCHEMBL13339889

SCHEMBL13339889

C[C@H](Nc1cncc(-c2ccc(N3CCOCC3)cc2)n1)c1cccc(NC(=O)c2cccnc2)c1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CSF1R P07333 13/20 0.66
SMN1; SMN2 Q16637 3/20 0.56
TP53 P04637 1/20 0.56
BRAF P15056 1/20 0.53
MEN1 O00255 1/20 0.51
KMT2A Q03164 1/20 0.51
RET P07949 1/20 0.50
PDGFRB P09619 1/20 0.50
KIT P10721 1/20 0.50
SRC P12931 1/20 0.50
PDGFRA P16234 1/20 0.50
FLT1 P17948 1/20 0.50
FLT4 P35916 1/20 0.50
KDR P35968 1/20 0.50
FRK P42685 1/20 0.50
DDR1 Q08345 1/20 0.50
MAPT P10636 2/20 0.48
NPC1 O15118 1/20 0.47
GAA P10253 1/20 0.47
RAB9A P51151 1/20 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
SCHEMBL19447205 0.91 CSF1R (0.63) CSF1RBRAFRETPDGFRBKIT
SCHEMBL13340090 0.91 CSF1R (0.63) CSF1RBRAFRETPDGFRBKIT
SCHEMBL13340035 0.91 CSF1R (0.63) CSF1RBRAFRETPDGFRBKIT
SCHEMBL19447236 0.91 CSF1R (0.63) CSF1RBRAFRETPDGFRBKIT
SCHEMBL13339849 0.86 CSF1R (0.75) CSF1RSMN1; SMN2RETPDGFRBKIT
SCHEMBL13339854 0.86 CSF1R (0.77) CSF1RSMN1; SMN2RETPDGFRBKIT
SCHEMBL16573051 0.85 CSF1R (0.73) CSF1RSMN1; SMN2TP53RETPDGFRB
SCHEMBL13339893 0.85 CSF1R (0.76) CSF1RSMN1; SMN2TP53RETPDGFRB
SCHEMBL13339852 0.85 CSF1R (0.76) CSF1RSMN1; SMN2TP53RETPDGFRB
SCHEMBL13340266 0.85 CSF1R (0.61) CSF1RBRAFRETPDGFRBKIT

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
EP-2848610-B1 Inhibitors of kinase activity YM BIOSCIENCES AUSTRALIA PTY (AU) 2017-10-11 EP disclosed
US-9029386-B2 Pyridine derivatives useful as kinase inhibitors GILEAD SCIENCES, INC. (US) 2015-05-12 US disclosed
US-20140178503-A1 CYCLOHEXYL UREA MODULATORS OF D2 RECEPTORS AND/OR D3 RECEPTORS AUSPEX PHARMACEUTICALS, INC. (US) 2014-06-26 US disclosed
US-8461161-B2 Substituted pyrazines as inhibitors of kinase activity YM BIOSCIENCES AUSTRALIA PTY LTD (AU) 2013-06-11 US disclosed
US-8461161-B2 Substituted pyrazines as inhibitors of kinase activity YM BIOSCIENCES AUSTRALIA PTY LTD (AU) 2013-06-11 US disclosed
US-20130137660-A1 INHIBITORS OF KINASE ACTIVITY YM BIOSCIENCES AUSTRALIA PTY LTD (AU) 2013-05-30 US disclosed
US-20100130447-A1 INHIBITORS OF KINASE ACTIVITY YM BIOSCIENCES AUSTRALIA PTY LTD (AU) 2010-05-27 US disclosed
US-20100130447-A1 INHIBITORS OF KINASE ACTIVITY YM BIOSCIENCES AUSTRALIA PTY LTD (AU) 2010-05-27 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 (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-20130137660-A1 INHIBITORS OF KINASE ACTIVITY FRK, LCK, FLT3 CSF1R 62/4885SMN1; SMN2 4319/4885TP53 818/4885
US-20100130447-A1 INHIBITORS OF KINASE ACTIVITY FRK, LCK, FLT3 CSF1R 62/4885SMN1; SMN2 4319/4885TP53 818/4885
US-20140178503-A1 CYCLOHEXYL UREA MODULATORS OF D2 RECEPTORS AND/OR D3 RECEPTORS UTS2R, VDR, PTGDR CSF1R 1931/4885SMN1; SMN2 4877/4885TP53 2070/4885

“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.