SCHEMBL4915443

SCHEMBL4915443

COc1ccccc1C[PH](=O)Cc1ccccc1

nearest known ligand 0.48

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.48
NPC1 O15118 1/20 0.48
RAB9A P51151 1/20 0.48
KMT2A Q03164 1/20 0.48
ABCB1 P08183 1/20 0.47
L3MBTL1 Q9Y468 2/20 0.46
HTT P42858 1/20 0.46
TAAR1 Q96RJ0 2/20 0.46
IDO1 P14902 2/20 0.44
KCNH2 Q12809 1/20 0.44
HPGD P15428 1/20 0.43
CHRM2 P08172 1/20 0.43
CHRM1 P11229 1/20 0.43
SIGMAR1 Q99720 1/20 0.42
ALDH1A1 P00352 1/20 0.42
GAA P10253 1/20 0.42
MAPT P10636 1/20 0.42
KDM4E B2RXH2 1/20 0.42
ALOX15 P16050 1/20 0.42

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
SCHEMBL22829797 0.77 L3MBTL1 (0.47) MEN1NPC1RAB9AKMT2AABCB1
SCHEMBL10337282 0.77 HTT (0.44) KMT2AL3MBTL1HTTTAAR1IDO1
SCHEMBL1322 0.77 MAOB (0.46) IDO1HPGDALDH1A1ALOX15
SCHEMBL10776123 0.77 IDO1 (0.48) MEN1NPC1RAB9AKMT2AL3MBTL1
SCHEMBL4877002 0.77 IDO1 (0.48) L3MBTL1HTTTAAR1IDO1HPGD
Ammonia Solution, Strong SCHEMBL10777161 0.75 IDO1 (0.47) MEN1NPC1RAB9AKMT2AL3MBTL1
SCHEMBL621779 0.74 HTR1A (0.58) ABCB1L3MBTL1TAAR1IDO1HPGD
SCHEMBL28603322 0.73 ABCB1 (0.52) KMT2AABCB1L3MBTL1HTTTAAR1
SCHEMBL10660614 0.73 ABCB1 (0.51) MEN1NPC1RAB9AKMT2AABCB1
SCHEMBL7335269 0.72 ABCB1 (0.80) ABCB1TAAR1KCNH2SIGMAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8471067-B2 Stereoselective preparation of P-chiral four-co-ordinated phosphorus compound (o-Tolylphenylmethylphosphine oxide) by reacting chiral alcohol, chiral amine or chiral thiol, with P-chiral three-co-ordinated phosphorus compound, in presence of electrophile UNIVERSITY COLLEGE DUBLIN (IE) 2013-06-25 US disclosed
US-20080255391-A1 Chiral Phosphorus Compounds UNIVERSITY COLLEGE DUBLIN NATIONAL UNIVERSITY OF IRELAND (IE) 2008-10-16 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-20080255391-A1 Chiral Phosphorus Compounds PHOSPHO1, PNKP, PTMS MEN1 3668/4885NPC1 4277/4885RAB9A 2627/4885

“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.