SCHEMBL4881756

SCHEMBL4881756

COc1ccc2c(c1OC)C(=O)C(CC1CCNCC1)C2

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 5/20 0.54
KDM4E B2RXH2 1/20 0.40
LMNA P02545 1/20 0.40
FAAH O00519 1/20 0.40
ABCC4 O15439 1/20 0.40
CACNA1F O60840 1/20 0.40
PDE5A O76074 1/20 0.40
ABCB11 O95342 1/20 0.40
APP P05067 1/20 0.40
BCHE P06276 1/20 0.40
CHRM2 P08172 1/20 0.40
ABCB1 P08183 1/20 0.40
CYP3A4 P08684 1/20 0.40
CHRM5 P08912 1/20 0.40
ADRA2A P08913 1/20 0.40
CHRM1 P11229 1/20 0.40
ADRA2C P18825 1/20 0.40
DRD4 P21917 1/20 0.40
SLC6A2 P23975 1/20 0.40
MAOB P27338 1/20 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
SCHEMBL15430938 0.80 ACHE (0.43) ACHEFAAHABCC4CACNA1FPDE5A
SCHEMBL4878163 0.78 ACHE (0.68) ACHEKDM4EFAAHABCC4CACNA1F
SCHEMBL4877278 0.78 ACHE (0.54) ACHEFAAHABCC4CACNA1FPDE5A
SCHEMBL1114944 0.76 ACHE (0.63) ACHEKDM4EFAAHABCC4CACNA1F
SCHEMBL29550221 0.76 ACHE (0.63) ACHEKDM4EFAAHABCC4CACNA1F
Hydrochloric Acid SCHEMBL4833887 0.75 ACHE (0.61) ACHEKDM4EFAAHABCC4CACNA1F
SCHEMBL28409784 0.75 ACHE (0.61) ACHEKDM4EFAAHABCC4CACNA1F
SCHEMBL4843083 0.74 METAP1 (0.58) ACHEFAAHABCC4CACNA1FPDE5A
SCHEMBL14156625 0.73 ACHE (0.54) ACHEKDM4EFAAHABCC4CACNA1F
SCHEMBL4834272 0.72 METAP1 (0.60) ACHEFAAHABCC4CACNA1FPDE5A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7446203-B2 Preparation of intermediates for acetycholinesterase inhibitors HETERO DRUGS LIMITED (IN) 2008-11-04 US disclosed
EP-1654230-A1 PREPARATION OF INTERMEDIATES FOR ACETYL CHOLINESTERASE INHIBITORS Hetero Drugs Limited (IN) 2006-05-10 EP disclosed
US-20060041140-A1 5,6-dimethoxy-2-(4-pyridyl)methyl-1-indanone is hydrogenated using platinum oxide catalyst in the presence of hydrochloric acid under a pressure of 2 bars to give 4-[(5,6-dimethoxy-1-indanon)-2-yl]methylpiperidine hydrochloride HETERO DRUGS LIMITED (IN) 2006-02-23 US disclosed
WO-2005003092-A1 PREPARATION OF INTERMEDIATES FOR ACETYL CHOLINESTERASE INHIBITORS HETERO DRUGS LIMITED (IN) 2005-01-13 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-20060041140-A1 5,6-dimethoxy-2-(4-pyridyl)methyl-1-indanone is hydrogenated using platinum oxide catalyst in the presence of hydrochloric acid under a pressure of 2 bars to give 4-[(5,6-dimethoxy-1-indanon)-2-yl]methylpiperidine hydrochloride ACHE, IDH2, IMPDH2 ACHE 1/4885KDM4E 51/4885LMNA 3997/4885

“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.