SCHEMBL9906182

SCHEMBL9906182

CC(C)C(CNc1ccccc1)NP(=O)(c1ccccc1)c1ccccc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.46
CYP3A4 P08684 8/20 0.39
TSHR P16473 6/20 0.39
MAPT P10636 4/20 0.39
CYP1A2 P05177 4/20 0.39
CYP2C9 P11712 4/20 0.39
CYP2C19 P33261 4/20 0.39
TP53 P04637 3/20 0.39
MEN1 O00255 2/20 0.39
CYP2D6 P10635 2/20 0.39
KMT2A Q03164 2/20 0.39
MAPK1 P28482 2/20 0.39
SMN1; SMN2 Q16637 3/20 0.36
HPGD P15428 2/20 0.36
GAA P10253 1/20 0.36
ALDH1A1 P00352 4/20 0.36
KDM4E B2RXH2 2/20 0.36
HSD17B10 Q99714 2/20 0.36
HTT P42858 2/20 0.36
NPSR1 Q6W5P4 1/20 0.36

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
SCHEMBL9906183 0.82 CYP3A4 (0.45) LMNACYP3A4TSHRMAPTCYP1A2
SCHEMBL11991381 0.72 MEN1 (0.46) MAPTMEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL23364960 0.72 MAPT (0.40) LMNACYP3A4TSHRMAPTCYP1A2
SCHEMBL3685456 0.72 MAPT (0.40) LMNACYP3A4TSHRMAPTCYP1A2
SCHEMBL23364961 0.72 MAPT (0.40) LMNACYP3A4TSHRMAPTCYP1A2
SCHEMBL28731719 0.72 ALDH1A1 (0.47) LMNACYP3A4TSHRMAPTCYP1A2
SCHEMBL23376913 0.71 MAPT (0.41) LMNACYP3A4TSHRMAPTCYP1A2
SCHEMBL9906156 0.71 MAPT (0.41) LMNACYP3A4TSHRMAPTCYP1A2
SCHEMBL9906161 0.71 MAPT (0.41) LMNACYP3A4TSHRMAPTCYP1A2
SCHEMBL9906160 0.71 MAPT (0.41) LMNACYP3A4TSHRMAPTCYP1A2

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-8198445-B2 Phosphoramide compound, method for producing the same, ligand, complex, catalyst and method for producing optically active alcohol NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY (JP) 2012-06-12 US disclosed
US-20100113786-A1 PHOSPHORAMIDE COMPOUND, METHOD FOR PRODUCING THE SAME, LIGAND, COMPLEX, CATALYST AND METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY (JP) 2010-05-06 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-20100113786-A1 PHOSPHORAMIDE COMPOUND, METHOD FOR PRODUCING THE SAME, LIGAND, COMPLEX, CATALYST AND METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL ADH1C, ADH1A, DERA LMNA 2701/4885CYP3A4 1529/4885TSHR 2806/4885

“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.