SCHEMBL4844028

SCHEMBL4844028

N#Cc1cc(C(=O)c2ccc(C(=O)O)cc2)cc2c1OCCC2

nearest known ligand 0.40

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.40
SRD5A2 P31213 7/20 0.39
CTNNB1 P35222 2/20 0.38
WNT3A P56704 2/20 0.38
NPC1 O15118 1/20 0.37
RAB9A P51151 1/20 0.37
XDH P47989 1/20 0.36
SLC22A12 Q96S37 1/20 0.36
KDM4E B2RXH2 1/20 0.35
MAPT P10636 1/20 0.35
KDM1A O60341 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
SCHEMBL14194548 0.77 NSD2 (0.41) ALDH1A1SRD5A2CTNNB1WNT3AMAPT
SCHEMBL4851383 0.76 ALDH1A1 (0.39) ALDH1A1CTNNB1WNT3AXDHSLC22A12
SCHEMBL29915036 0.69 PARP1 (0.41) ALDH1A1KDM4EMAPT
SCHEMBL27002417 0.69 PARP1 (0.41) ALDH1A1KDM4EMAPT
SCHEMBL31262479 0.68 CTNNB1 (0.67) ALDH1A1CTNNB1WNT3ANPC1RAB9A
SCHEMBL875455 0.68 CTNNB1 (0.67) ALDH1A1CTNNB1WNT3ANPC1RAB9A
SCHEMBL4733998 0.68 MAOB (0.38) NPC1RAB9AXDHSLC22A12MAPT
SCHEMBL14124788 0.67 ALDH1A1 (0.79) ALDH1A1SRD5A2NPC1RAB9AKDM4E
SCHEMBL14124796 0.67 ALDH1A1 (0.72) ALDH1A1SRD5A2CTNNB1WNT3ANPC1
SCHEMBL4695076 0.66 PARP1 (0.38) ALDH1A1KDM4EMAPT

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-7351737-B2 4-[(8-substituted)-6-chromanoyl]-and 4-[8-substituted)-chroman-6-YL-ethynyl]-benzoic and phenylacetic acids, their esters and salts having cytochrome P450RAI inhibitory activity ALLERGAN, INC. (US) 2008-04-01 US disclosed
EP-1485368-A1 SUBSTITUTED CHROMAN DERIVATIVES HAVING CYTOCHROME P450RAI INHIBITORY ACTIVITY Allergan, Inc. (US) 2004-12-15 EP disclosed
US-20040077721-A1 Compositions and methods using compounds having cytochrome P450RAI inhibitory activity co-administered with vitamin A ALLERGAN, INC. 2004-04-22 US disclosed
US-20030207937-A1 4-[(8-Substituted)-6-chromanoyl]-and 4-[8-substituted)-chroman-6-yl-ethynyl]-benzoic and phenylacetic acids, their esters and salts having cytochrome P450RAI inhibitory activity ALLERGAN, INC. 2003-11-06 US disclosed
WO-2003080594-A1 SUBSTITUTED CHROMAN DERIVATIVES HAVING CYTOCHROME P450RAI INHIBITORY ACTIVITY ALLERGAN, INC. (US) 2003-10-02 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 (2 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-20040077721-A1 Compositions and methods using compounds having cytochrome P450RAI inhibitory activity co-administered with vitamin A RARA, CYP2R1, RXRA ALDH1A1 154/4885SRD5A2 202/4885CTNNB1 3935/4885
US-20030207937-A1 4-[(8-Substituted)-6-chromanoyl]-and 4-[8-substituted)-chroman-6-yl-ethynyl]-benzoic and phenylacetic acids, their esters and salts having cytochrome P450RAI inhibitory activity RXRA, RARA, CYP26A1 ALDH1A1 60/4885SRD5A2 129/4885CTNNB1 3415/4885

“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.