SCHEMBL1448955

SCHEMBL1448955

CC(=O)c1ccccc1-c1ccccc1Pc1ccccc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4C Q9H3R0 1/20 0.41
CYP3A4 P08684 1/20 0.38
CYP2C9 P11712 1/20 0.38
ALOX12 P18054 1/20 0.38
MEN1 O00255 2/20 0.36
KMT2A Q03164 2/20 0.36
DAPK3 O43293 1/20 0.35
JAK2 O60674 1/20 0.35
PRKD3 O94806 1/20 0.35
MAP4K4 O95819 1/20 0.35
PAK4 O96013 1/20 0.35
ABL1 P00519 1/20 0.35
CSF1R P07333 1/20 0.35
RET P07949 1/20 0.35
MET P08581 1/20 0.35
PDGFRB P09619 1/20 0.35
PIM1 P11309 1/20 0.35
FGFR1 P11362 1/20 0.35
PDGFRA P16234 1/20 0.35
PRKACA P17612 1/20 0.35

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
SCHEMBL1452441 0.86 CYP3A4 (0.47) CYP3A4CYP2C9ALOX12KMT2AMYC
SCHEMBL18715445 0.85 ALDH1A1 (0.39) KDM4CMEN1KMT2AFFAR1SMN1; SMN2
SCHEMBL27932099 0.79 THRB (0.38) KMT2AFFAR1SMN1; SMN2ALDH1A1ALOX15
SCHEMBL4061116 0.79 CA12 (0.32) MEN1KMT2ACA12CA1CA2
SCHEMBL978600 0.79 KDM4C (0.50) KDM4CCYP3A4CYP2C9ALOX12MEN1
SCHEMBL9223049 0.75 CYP3A4 (0.60) KDM4CCYP3A4CYP2C9ALOX12MYC
SCHEMBL10702548 0.74 ALDH1A1 (0.54) KMT2ASMN1; SMN2ALDH1A1ALOX15CA12
SCHEMBL27931995 0.72 TP53 (0.35) CYP2C9MEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL2556230 0.72 HPGD (0.46) CYP3A4CYP2C9MEN1KMT2ASMN1; SMN2
SCHEMBL5951434 0.72 BCAT2 (0.53) KDM4CMEN1KMT2ASMN1; SMN2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7910744-B2 Pyrazole and Pyrimidine groups are introduced on aromatic phosphine; (3-bromophenyl)methyl ketone and ethylene glycol cyclize to [3-(2-methyl-1,3-dioxolane-2-yl)phenyl]diphenylphosphane; adding hydrazine monohydrate, then oxidizing with hydrogen peroxide; [3-(3-Pyrazolyl)phenyl]diphenylphosphane oxide ZYLUM BETEILIGUNGSGESELLSCHAFT MBH & CO. PATENT II KG (DE) 2011-03-22 US disclosed
EP-1805193-B1 METHOD FOR THE PRODUCTION OF SUBSTITUTED PHOSPHANES ZYLUM BETEILIGUNGSGMBH & CO PATENTE II KG (DE) 2010-12-29 EP disclosed
US-20080221335-A1 Method for the Manufacture of Substituted Phosphanes, and Substituted Phosphanes Manufactured According to Said Method ZYLUM BETEILIGUNGSGESELLSCHAFT MBH & CO. PATENTE II KG (DE) 2008-09-11 US disclosed
EP-1805193-A1 METHOD FOR THE PRODUCTION OF SUBSTITUTED PHOSPHANES, AND SUBSTITUTED PHOSPHANES PRODUCED ACCORDING TO SAID METHOD Technische Universität Chemnitz (DE) 2007-07-11 EP disclosed
WO-2006045272-A1 METHOD FOR THE PRODUCTION OF SUBSTITUTED PHOSPHANES, AND SUBSTITUTED PHOSPHANES PRODUCED ACCORDING TO SAID METHOD TECHNISCHE UNIVERSITÄT CHEMNITZ (DE) 2006-05-04 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-20080221335-A1 Method for the Manufacture of Substituted Phosphanes, and Substituted Phosphanes Manufactured According to Said Method SCLY, SELENOI, TST KDM4C 1758/4885CYP3A4 1370/4885CYP2C9 892/4885

“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.