SCHEMBL6929865

SCHEMBL6929865

O=C(O)C(ON1CCCC1)c1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.50
GAA P10253 1/20 0.49
ALDH1A1 P00352 3/20 0.43
KMT2A Q03164 2/20 0.43
MEN1 O00255 1/20 0.43
KDM4E B2RXH2 2/20 0.41
MAPT P10636 1/20 0.41
HPGD P15428 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
CYP2D6 P10635 5/20 0.41
CYP1A2 P05177 4/20 0.41
CYP3A4 P08684 4/20 0.41
CYP2C9 P11712 4/20 0.41
KCNA5 P22460 4/20 0.41
CYP2C19 P33261 4/20 0.41
KCNH2 Q12809 4/20 0.41
CHRM1 P11229 1/20 0.41
SRC P12931 1/20 0.41
KCNE1 P15382 1/20 0.40
MITF O75030 2/20 0.40

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
Carbamic Acid SCHEMBL17460309 0.77 GAA (0.47) LMNAGAAALDH1A1KMT2AMEN1
SCHEMBL28042294 0.77 CYP2D6 (0.50) LMNAGAACYP2D6CYP1A2CYP3A4
SCHEMBL1802065 0.75 CYP3A4 (0.52) LMNAGAAALDH1A1KMT2AMEN1
Hydrochloric Acid SCHEMBL7654483 0.73 CYP3A4 (0.50) LMNAGAAALDH1A1KMT2AMEN1
SCHEMBL8400939 0.72 SRC (0.54) LMNAALDH1A1KMT2AKDM4ECYP2D6
SCHEMBL7332031 0.71 SLC6A4 (0.57) CYP2D6CYP1A2CYP3A4CYP2C19KCNH2
SCHEMBL7480934 0.70 CYP2D6 (0.47) LMNAGAAALDH1A1KMT2AMEN1
SCHEMBL5859624 0.70 CYP1A2 (0.47) LMNAGAAALDH1A1KMT2AMEN1
SCHEMBL974061 0.70 SRC (0.52) LMNAALDH1A1KMT2AKDM4ECYP2D6
SCHEMBL11404609 0.70 SRC (0.52) LMNAALDH1A1KMT2AKDM4ECYP2D6

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-6515142-B2 Intermediates of aromatic amidine derivatives which have anticoagulation action DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2003-02-04 US disclosed
US-20020062033-A1 Process for preparing 2-phenyl-3-naphthylpropionic acid derivatives DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2002-05-23 US disclosed
US-6337405-B1 MULTISTAGE REACTION OF PYRROLE SUBSTITUTED WITH SULFONATE GROUPS AND HYDROXYPHENYLACETIC ACID DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2002-01-08 US disclosed
US-6252088-B1 COUPLING A NITRILE CONTAININ NAPHTHALENE COMPOUND WITH A COMPOUND CONTAINING PROPIONIC ACID GROUP DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2001-06-26 US disclosed
EP-0936215-A1 PROCESS FOR PREPARING 2-PHENYL-3-NAPHTHYLPROPIONIC ACID DERIVATIVES DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1999-08-18 EP 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-20020062033-A1 Process for preparing 2-phenyl-3-naphthylpropionic acid derivatives PROC, F12, F2 LMNA 283/4885GAA 2260/4885ALDH1A1 2372/4885

“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.