SCHEMBL817343

SCHEMBL817343

CC1=C(O[Si](C)(C)C)c2ccccc2CC1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES1 P23141 1/20 0.41
CYP19A1 P11511 3/20 0.37
CYP11B2 P19099 3/20 0.37
CYP11B1 P15538 2/20 0.37
CYP17A1 P05093 1/20 0.37
SETD7 Q8WTS6 1/20 0.37
TYMS P04818 1/20 0.36
NOS3 P29474 1/20 0.35
NOS2 P35228 1/20 0.35
SMN1; SMN2 Q16637 2/20 0.35
MAOA P21397 1/20 0.34
MAOB P27338 1/20 0.34
KDM4E B2RXH2 3/20 0.34
ALDH1A1 P00352 3/20 0.34
POLB P06746 1/20 0.34
MIF P14174 1/20 0.34
HPGD P15428 2/20 0.34
TDP1 Q9NUW8 2/20 0.34
L3MBTL1 Q9Y468 2/20 0.34
GLA P06280 1/20 0.34

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
SCHEMBL817028 0.83 MAOA (0.38) CES1SMN1; SMN2MAOAMAOBKDM4E
SCHEMBL7554989 0.71 CES1 (0.50) CES1CYP19A1CYP11B2CYP11B1CYP17A1
SCHEMBL29446604 0.69 CES1 (0.35) CES1SETD7TYMSNOS3NOS2
SCHEMBL8772548 0.69 CES1 (0.35) CES1SETD7TYMSNOS3NOS2
SCHEMBL24287303 0.68 CES1 (0.46) CES1CYP19A1CYP11B2CYP11B1CYP17A1
SCHEMBL8534624 0.68 CES1 (0.46) CES1CYP19A1CYP11B2CYP11B1CYP17A1
SCHEMBL19645160 0.68 CES1 (0.46) CES1CYP19A1CYP11B2CYP11B1CYP17A1
SCHEMBL22810220 0.68 CES1 (0.46) CES1CYP19A1CYP11B2CYP11B1CYP17A1
SCHEMBL28445132 0.68 HRH1 (0.35) MAOAMAOBCYP1A2CHRM2CHRM4
SCHEMBL10802799 0.67

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-7906651-B2 Catalytic system of asymmetric reactions in aqueous media; react a silicon enolate and formaldehyde; catalyst obtained by mixing chiral ligands with scandium triflate JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2011-03-15 US disclosed
US-20080269496-A1 Method for Producing Optically Active Hydroxymethylated Compounds JAPAN SCIENCE AND TECHNOLOGY AGENCY (JP) 2008-10-30 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-20080269496-A1 Method for Producing Optically Active Hydroxymethylated Compounds TET1, TET3, CYP3A4 CES1 1286/4885CYP19A1 108/4885CYP11B2 72/4885

“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.