SCHEMBL1264765

SCHEMBL1264765

O=C1c2ccccc2C(=O)N1c1nccc2ccccc12

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 1/20 0.54
ALDH1A1 P00352 4/20 0.50
SMN1; SMN2 Q16637 2/20 0.50
NPC1 O15118 1/20 0.50
MAPT P10636 1/20 0.50
RAB9A P51151 1/20 0.50
COMT P21964 1/20 0.49
HRH4 Q9H3N8 1/20 0.47
HTR2C P28335 1/20 0.47
KDM4E B2RXH2 2/20 0.45
GAA P10253 1/20 0.45
HTT P42858 2/20 0.43
CYP2A6 P11509 1/20 0.43
F12 P00748 1/20 0.43
PLAU P00749 1/20 0.43
NCF1 P14598 1/20 0.43
NOS3 P29474 1/20 0.43
NOS1 P29475 1/20 0.43
NOS2 P35228 1/20 0.43
BACE1 P56817 1/20 0.43

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
SCHEMBL5133259 0.82 CYP3A4 (0.46) POLBALDH1A1SMN1; SMN2NPC1MAPT
SCHEMBL14895927 0.77 PDPK1 (0.40) POLBALDH1A1SMN1; SMN2NPC1MAPT
SCHEMBL5133459 0.77 SCN2A (0.50) POLBALDH1A1MAPTKDM4EMEN1
SCHEMBL11006460 0.74 MAPT (0.44) POLBALDH1A1SMN1; SMN2NPC1MAPT
SCHEMBL14896334 0.74 HTT (0.35) POLBALDH1A1SMN1; SMN2NPC1MAPT
SCHEMBL14908385 0.74 GABRP (0.36) POLBALDH1A1KDM4EGAAHTT
SCHEMBL5202901 0.74 COMT (0.58) ALDH1A1SMN1; SMN2NPC1MAPTRAB9A
SCHEMBL16432053 0.73 LMNA (0.42) HTTMEN1LMNAKMT2AMAOA
SCHEMBL7560710 0.72 HRH4 (0.58) HRH4HTR2C
SCHEMBL23860829 0.72 MEN1 (0.45) POLBALDH1A1SMN1; SMN2KDM4EGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7893071-B2 Substituted phthalimide and isoquinoline derivatives; thalidomide analogs that lack the piperidine-2,6-dione moiety of thalidomide UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2011-02-22 US disclosed
US-7893071-B2 Substituted phthalimide and isoquinoline derivatives; thalidomide analogs that lack the piperidine-2,6-dione moiety of thalidomide UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2011-02-22 US disclosed
US-7893071-B2 Substituted phthalimide and isoquinoline derivatives; thalidomide analogs that lack the piperidine-2,6-dione moiety of thalidomide UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2011-02-22 US disclosed
EP-1389103-A4 SYNTHESIS AND EVALUATION OF NOVEL PHTHALIMIDE MIMICS AS ANTI-ANGIOGENIC AGENTS UNIV VIRGINIA (US) 2005-09-14 EP disclosed
US-20040122030-A1 Synthesis and evaluation of novel phthalimide mimics as anti-angiogenic UNIVERSITY OF VIRGINIA PATENT FOUNDATION 2004-06-24 US disclosed
EP-1389103-A2 SYNTHESIS AND EVALUATION OF NOVEL PHTHALIMIDE MIMICS AS ANTI-ANGIOGENIC AGENTS THE UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2004-02-18 EP disclosed
WO-2002086078-A2 SYNTHESIS AND EVALUATION OF NOVEL PHTHALIMIDE MIMICS AS ANTI-ANGIOGENIC AGENTS UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2002-10-31 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 (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-20040122030-A1 Synthesis and evaluation of novel phthalimide mimics as anti-angiogenic KDR, FLT4, FLT1 POLB 3460/4885ALDH1A1 1161/4885SMN1; SMN2 4043/4885

“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.