SCHEMBL7451235

SCHEMBL7451235

NC[C@@H]1O[C@@H](C23CC4CC(CC(C4)C2)C3)Cc2c1ccc(O)c2O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DRD1 P21728 19/20 1.00
KDM4E B2RXH2 3/20 1.00
MAPT P10636 3/20 1.00
MEN1 O00255 2/20 1.00
KMT2A Q03164 2/20 1.00
TDP1 Q9NUW8 2/20 1.00
TP53 P04637 2/20 1.00
CYP3A4 P08684 2/20 1.00
CYP2D6 P10635 2/20 1.00
CYP2C19 P33261 2/20 1.00
NPC1 O15118 1/20 1.00
ALDH1A1 P00352 1/20 1.00
DRD2 P14416 1/20 1.00
HPGD P15428 1/20 1.00
NFKB1 P19838 1/20 1.00
MAPK1 P28482 1/20 1.00
THPO P40225 1/20 1.00
MTOR P42345 1/20 1.00
RAB9A P51151 1/20 1.00
HIF1A Q16665 1/20 1.00

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
SCHEMBL20785596 1.00 DRD1 (1.00) DRD1KDM4EMAPTMEN1KMT2A
SCHEMBL20785604 1.00 DRD1 (1.00) DRD1KDM4EMAPTMEN1KMT2A
SCHEMBL400069 1.00 DRD1 (1.00) DRD1KDM4EMAPTMEN1KMT2A
SCHEMBL7445628 1.00 DRD1 (1.00) DRD1KDM4EMAPTMEN1KMT2A
SCHEMBL1081313 1.00 DRD1 (1.00) DRD1KDM4EMAPTMEN1KMT2A
Hydrochloric Acid SCHEMBL30928211 0.99 DRD1 (1.00) DRD1KDM4EMAPTMEN1KMT2A
Hydrochloric Acid SCHEMBL30914176 0.99 DRD1 (1.00) DRD1KDM4EMAPTMEN1KMT2A
Hydrochloric Acid SCHEMBL29390394 0.99 DRD1 (1.00) DRD1KDM4EMAPTMEN1KMT2A
Hydrochloric Acid SCHEMBL1878106 0.99 DRD1 (1.00) DRD1KDM4EMAPTMEN1KMT2A
Hydrochloric Acid SCHEMBL5808372 0.99 DRD1 (1.00) DRD1KDM4EMAPTMEN1KMT2A

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 3 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