SCHEMBL3141602

SCHEMBL3141602

O=C(Nc1ccc(C(F)(F)F)cc1)c1cccnc1NCc1ccnc(N2CCOCC2)c1

nearest known ligand 0.68

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
ABCB1 P08183 1/20 0.68
KDR P35968 12/20 0.66
SMN1; SMN2 Q16637 2/20 0.50
MAPT P10636 1/20 0.50
STAT3 P40763 1/20 0.50
AURKA O14965 1/20 0.49
RPS6KB1 P23443 1/20 0.49
RAF1 P04049 2/20 0.48
BRAF P15056 2/20 0.48
KDM4E B2RXH2 1/20 0.47
GAA P10253 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
SCHEMBL3151940 0.93 ABCB1 (0.63) ABCB1KDRMAPTAURKARPS6KB1
SCHEMBL3156373 0.92 KDR (0.69) ABCB1KDRSMN1; SMN2MAPTKDM4E
SCHEMBL3159205 0.85 KDR (0.59) ABCB1KDRAURKARPS6KB1
SCHEMBL3155127 0.85 ABCB1 (0.57) ABCB1KDRAURKARPS6KB1RAF1
SCHEMBL445700 0.84 KDR (0.60) ABCB1KDRAURKARPS6KB1
SCHEMBL3147790 0.82 KDR (0.50) ABCB1KDRAURKARPS6KB1RAF1
SCHEMBL13417797 0.82 KDR (0.50) ABCB1KDRAURKARPS6KB1RAF1
SCHEMBL426633 0.81 ABCB1 (1.00) ABCB1KDRMAPTRAF1BRAF
SCHEMBL427743 0.81 KDR (1.00) ABCB1KDRRAF1BRAF
Hydrochloric Acid SCHEMBL448409 0.80 ABCB1 (0.98) ABCB1KDRMAPTRAF1BRAF

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-20050261313-A1 Substituted alkylamine derivatives and methods of use AMGEN INC. 2005-11-24 US claimed
EP-1537084-A1 SUBSTITUTED 2-ALKYLAMINE NICOTINIC AMIDE DERIVATIVES AND USE THERE OF Amgen Inc. (US) 2005-06-08 EP claimed
US-6878714-B2 Substituted alkylamine derivatives and methods of use AMGEN INC. (US) 2005-04-12 US claimed
WO-2004007458-A1 SUBSTITUTED 2-ALKYLAMINE NICOTINIC AMIDE DERIVATIVES AND USE THERE OF AMGEN INC. (US) 2004-01-22 WO claimed
US-20030225106-A1 Substituted alkylamine derivatives and methods of use AMGEN INC. 2003-12-04 US claimed
US-7687643-B2 Process for preparing 3,3-dimethylindolines AMGEN INC. (US) 2010-03-30 US disclosed
US-7687643-B2 Process for preparing 3,3-dimethylindolines AMGEN INC. (US) 2010-03-30 US disclosed
US-7687643-B2 Process for preparing 3,3-dimethylindolines AMGEN INC. (US) 2010-03-30 US disclosed
US-20050261313-A1 Substituted alkylamine derivatives and methods of use AMGEN INC. 2005-11-24 US disclosed
EP-1537084-A1 SUBSTITUTED 2-ALKYLAMINE NICOTINIC AMIDE DERIVATIVES AND USE THERE OF Amgen Inc. (US) 2005-06-08 EP disclosed
US-6878714-B2 Substituted alkylamine derivatives and methods of use AMGEN INC. (US) 2005-04-12 US disclosed
WO-2004007458-A1 SUBSTITUTED 2-ALKYLAMINE NICOTINIC AMIDE DERIVATIVES AND USE THERE OF AMGEN INC. (US) 2004-01-22 WO disclosed
US-20030225106-A1 Substituted alkylamine derivatives and methods of use AMGEN INC. 2003-12-04 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-20030225106-A1 Substituted alkylamine derivatives and methods of use NAT1, PIGO, AADAC ABCB1 237/4885KDR 15/4885SMN1; SMN2 1447/4885
US-20050261313-A1 Substituted alkylamine derivatives and methods of use NAT1, PIGO, AADAC ABCB1 237/4885KDR 15/4885SMN1; SMN2 1447/4885

“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.