SCHEMBL3749883

SCHEMBL3749883

C=C[C@@H](C)[C@H](N)c1ccc(OC)cc1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.44
CYP2D6 P10635 1/20 0.44
CYP2C19 P33261 1/20 0.44
SLC6A4 P31645 1/20 0.43
CA1 P00915 2/20 0.41
CA2 P00918 2/20 0.41
ACHE P22303 1/20 0.41
ALDH1A1 P00352 6/20 0.41
TDP1 Q9NUW8 4/20 0.41
MAPK1 P28482 3/20 0.41
CYP3A4 P08684 3/20 0.41
ALOX15 P16050 2/20 0.41
ALOX12 P18054 2/20 0.41
KDM4E B2RXH2 2/20 0.41
USP2 O75604 1/20 0.41
MAPT P10636 1/20 0.41
HPGD P15428 1/20 0.41
CA12 O43570 1/20 0.41
CA7 P43166 1/20 0.41
CA9 Q16790 1/20 0.41

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
SCHEMBL2996389 1.00 CYP1A2 (0.44) CYP1A2CYP2D6CYP2C19SLC6A4CA1
SCHEMBL2996386 1.00 CYP1A2 (0.44) CYP1A2CYP2D6CYP2C19SLC6A4CA1
SCHEMBL13267800 1.00 CYP1A2 (0.44) CYP1A2CYP2D6CYP2C19SLC6A4CA1
SCHEMBL1900910 0.80 CA1 (0.58) CYP1A2CYP2D6CYP2C19SLC6A4CA1
SCHEMBL1900477 0.80 CA1 (0.58) CYP1A2CYP2D6CYP2C19SLC6A4CA1
SCHEMBL1305495 0.80 CA1 (0.58) CYP1A2CYP2D6CYP2C19SLC6A4CA1
SCHEMBL591062 0.80 CA1 (0.58) CYP1A2CYP2D6CYP2C19SLC6A4CA1
SCHEMBL13056306 0.79 DPP4 (0.36) ACHEALDH1A1TDP1MAPTCA7
SCHEMBL13056307 0.79 DPP4 (0.36) ACHEALDH1A1TDP1MAPTCA7
SCHEMBL8914585 0.79 CYP1A2 (0.48) CYP1A2CYP2D6CYP2C19SLC6A4CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8350047-B2 Methods of preparing secondary carbinamine compounds with boronic acids THADANI AVINASH N (CA) 2013-01-08 US disclosed
US-20100298572-A1 METHODS OF PREPARING SECONDARY CARBINAMINE COMPOUNDS WITH BORONIC ACIDS PANASONIC CORPORATION (JP) 2010-11-25 US disclosed
WO-2008119161-A1 METHODS OF PREPARING SECONDARY CARBINAMINE COMPOUNDS WITH BORONIC ACIDS KANATA CHEMICAL TECHNOLOGIES INC. (CA) 2008-10-09 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-20100298572-A1 METHODS OF PREPARING SECONDARY CARBINAMINE COMPOUNDS WITH BORONIC ACIDS C9, BCAT2, SLC1A5 CYP1A2 541/4885CYP2D6 1030/4885CYP2C19 959/4885

“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.