SCHEMBL7310836

SCHEMBL7310836

COc1ccc2c(c1OC)CC(c1ccccc1)C=C2CN

nearest known ligand 0.43

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ACHE P22303 1/20 0.43
ALDH1A1 P00352 3/20 0.37
KDM4E B2RXH2 2/20 0.37
HPGD P15428 1/20 0.37
CA1 P00915 1/20 0.36
CA2 P00918 1/20 0.36
CA4 P22748 1/20 0.36
CA6 P23280 1/20 0.36
KDM1A O60341 2/20 0.35
MAOB P27338 1/20 0.35
RAB9A P51151 2/20 0.33
NPC1 O15118 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
POLB P06746 1/20 0.33
PTGS2 P35354 1/20 0.33
GAA P10253 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
ADRA1A P35348 1/20 0.33

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
Hydrochloric Acid SCHEMBL7310685 0.99 ACHE (0.42) ACHEALDH1A1KDM4EHPGDCA1
SCHEMBL9802431 0.86 MAPT (0.39) ALDH1A1KDM4ERAB9ANPC1SMN1; SMN2
Hydrochloric Acid SCHEMBL9802239 0.85 MAPT (0.38) ALDH1A1KDM4ERAB9ANPC1SMN1; SMN2
SCHEMBL7447203 0.85 ACHE (0.35) ACHEKDM4EKDM1AMAOB
Hydrochloric Acid SCHEMBL9802508 0.85 ACHE (0.40) ACHE
SCHEMBL9038396 0.80 PTPN1 (0.37) ALDH1A1KDM4EHPGDSMN1; SMN2L3MBTL1
Hydrochloric Acid SCHEMBL7317155 0.79 PTPN1 (0.36) ALDH1A1KDM4EHPGDSMN1; SMN2L3MBTL1
SCHEMBL613008 0.79 ACHE (0.44) ACHEALDH1A1KDM4EHPGDCA1
SCHEMBL8829266 0.78 ELANE (0.34) L3MBTL1NPSR1
SCHEMBL7442764 0.74 GAA (0.39) ALDH1A1KDM4ERAB9ANPC1PTGS2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5621133-A PREPARING A 1-(3,4-DIALKOXYPHENYL),3-HYDROXYALKANE(C6-C12) BY EPOXIDIZING A HALO DERIVATIVE WITH A BASE FOLLOWED BY DECYCLICIZING WITH AN ORGANOMETALLIC COMPOUND IN A SOLVENT; NAPHTHYLENES, ISOCHROMENES AND ISOTHIOCHROMENES DENINNO MICHAEL P (US) 1997-04-15 US disclosed
US-5591884-A PROTECTED HYDROXYALKYLCATECHOL INTERMEDIATES ABBOTT LABORATORIES (US) 1997-01-07 US disclosed
EP-0474767-B1 DOPAMINE AGONISTS ABBOTT LAB (US) 1996-02-21 EP disclosed
EP-0474767-A4 DOPAMINE AGONISTS 1992-07-08 EP disclosed
EP-0474767-A1 DOPAMINE AGONISTS. ABBOTT LAB (US) 1992-03-18 EP disclosed
WO-1990015056-A1 DOPAMINE AGONISTS ABBOTT LABORATORIES (US) 1990-12-13 WO disclosed
US-4963568-A TREATMENT OF PARKINSON*S DISEASE, CARDIOVASCULAR DISORDERS ABBOTT LABORATORIES (US) 1990-10-16 US disclosed