SCHEMBL7312490

SCHEMBL7312490

CC(C)(C)OC(=O)NCC1=CC(c2ccccc2)Cc2c1ccc(O)c2O

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC1 Q13547 1/20 0.41
KDM4A O75164 1/20 0.37
NAMPT P43490 1/20 0.36
KDM1A O60341 1/20 0.35
MAOB P27338 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
KCNA5 P22460 1/20 0.35
ACACB O00763 3/20 0.35
ACACA Q13085 2/20 0.35
TLR2 O60603 1/20 0.35
TLR1 Q15399 1/20 0.35
CA12 O43570 1/20 0.34
CA1 P00915 1/20 0.34
CA7 P43166 1/20 0.34
CA14 Q9ULX7 1/20 0.34
ATM Q13315 1/20 0.34
BRD4 O60885 1/20 0.34
CREBBP Q92793 1/20 0.34
MALT1 Q9UDY8 1/20 0.34
IDO1 P14902 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
SCHEMBL9802835 0.88 HDAC1 (0.40) HDAC1KDM4ANAMPTKDM1AMAOB
SCHEMBL7446408 0.81 DRD2 (0.35) HDAC1KDM4ANAMPTKDM1AMAOB
SCHEMBL7315264 0.81 KDM4A (0.36) HDAC1KDM4ANAMPTKDM1AMAOB
Hydrochloric Acid SCHEMBL7447474 0.81 DRD2 (0.35) HDAC1KDM4ANAMPTKDM1AMAOB
SCHEMBL9802602 0.79 EPHX2 (0.37) HDAC1KDM4ANAMPTKDM1AMAOB
Hydrochloric Acid SCHEMBL7498114 0.74 DRD1 (0.37) CA1MAPT
Hydrochloric Acid SCHEMBL7307954 0.74 DRD1 (0.42) MAPT
Bromide SCHEMBL7318319 0.74 DRD1 (0.42) MAPT
SCHEMBL7447921 0.73 KMT2A (0.38) ATMKMT2A
SCHEMBL7447927 0.73 KMT2A (0.38) ATMKMT2A

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 8 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
WO-1996038435-A1 DOPAMINE AGONISTS ABBOTT LABORATORIES (US) 1996-12-05 WO 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