SCHEMBL1168002

SCHEMBL1168002

Nc1nc(Nc2ccc(N3CCOCC3)cc2)nn1C(=O)c1cccc(Cl)c1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AXL P30530 2/20 0.55
INSR P06213 1/20 0.55
MAPT P10636 3/20 0.52
ALDH1A1 P00352 1/20 0.52
TDP1 Q9NUW8 1/20 0.52
STAT6 P42226 1/20 0.50
KIT P10721 3/20 0.49
FLT3 P36888 3/20 0.49
CDK1 P06493 2/20 0.49
CCNB2 O95067 1/20 0.49
CCNB1 P14635 1/20 0.49
CCNB3 Q8WWL7 1/20 0.49
PLK4 O00444 1/20 0.48
JAK1 P23458 4/20 0.47
TYK2 P29597 4/20 0.47
JAK3 P52333 2/20 0.47
JAK2 O60674 2/20 0.47
CDK2 P24941 1/20 0.47
NPC1 O15118 1/20 0.46
RAB9A P51151 1/20 0.46

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
SCHEMBL1167094 0.89 AXL (0.55) AXLINSRMAPTSTAT6KIT
SCHEMBL1167567 0.86 JAK1 (0.54) AXLINSRKITFLT3CDK1
SCHEMBL1167499 0.86 CSF1R (0.56) AXLINSRMAPTALDH1A1STAT6
SCHEMBL1167779 0.85 MAPT (0.54) AXLINSRMAPTALDH1A1TDP1
SCHEMBL1168102 0.85 MAPT (0.52) MAPTALDH1A1TDP1STAT6PLK4
SCHEMBL1168367 0.84 AXL (0.59) AXLINSRMAPTKITFLT3
SCHEMBL1167417 0.82 AXL (0.60) AXLINSRMAPTALDH1A1TDP1
SCHEMBL1167944 0.82 RAB9A (0.54) MAPTCDK1CCNB2CCNB1CCNB3
SCHEMBL1167740 0.82 AXL (0.57) AXLINSRMAPTALDH1A1TDP1
SCHEMBL1167710 0.80 CDK1 (0.69) AXLINSRKITFLT3CDK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1922310-A2 TRIAZOLE DERIVATIVES USEFUL AS AXL INHIBITORS Rigel Pharmaceuticals, Inc. (US) 2008-05-21 EP claimed
US-20070213375-A1 Triazole derivatives useful as Axl inhibitors RIGEL PHARMACEUTICALS, INC. (US) 2007-09-13 US claimed
WO-2007030680-A2 TRIAZOLE DERIVATIVES USEFUL AS AXL INHIBITORS RIGEL PHARMACEUTICALS, INC. (US) 2007-03-15 WO claimed
US-8389557-B2 Triazole derivatives useful as Axl inhibitors RIGEL PHARMACEUTICALS, INC. (US) 2013-03-05 US disclosed
US-20110082131-A1 TRIAZOLE DERIVATIVES USEFUL AS AXL INHIBITORS RIGEL PHARMACEUTICALS, INC. (US) 2011-04-07 US disclosed
US-7884119-B2 protein tyrosine kinase receptor inhibitors such as 3-amino -1-(1H-indol-5-yl)carbonyl-5-[4-2-(pyrrolidin-1-yl)ethoxy]phenylamino]-1H-1,2,4-triazole, used for treating diseases and conditions associated with neovascularization and/or cell proliferation RIGEL PHARMACEUTICALS, INC. (US) 2011-02-08 US disclosed
EP-1922310-A2 TRIAZOLE DERIVATIVES USEFUL AS AXL INHIBITORS Rigel Pharmaceuticals, Inc. (US) 2008-05-21 EP disclosed
US-20070213375-A1 Triazole derivatives useful as Axl inhibitors RIGEL PHARMACEUTICALS, INC. (US) 2007-09-13 US disclosed
WO-2007030680-A2 TRIAZOLE DERIVATIVES USEFUL AS AXL INHIBITORS RIGEL PHARMACEUTICALS, INC. (US) 2007-03-15 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 (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-20110082131-A1 TRIAZOLE DERIVATIVES USEFUL AS AXL INHIBITORS AXL, TYRO3, FLT3 AXL 1/4885INSR 508/4885MAPT 2385/4885
US-20070213375-A1 Triazole derivatives useful as Axl inhibitors AXL, TYRO3, FLT3 AXL 1/4885INSR 291/4885MAPT 2368/4885

“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.