SCHEMBL7446689

SCHEMBL7446689

CC(=O)Oc1ccc2c(c1OC(C)=O)CC(c1ccccc1)C=C2CNC(=O)CC[C@H](N)C(=O)O

nearest known ligand 0.38

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
SLC1A1 P43005 2/20 0.38
LTA4H P09960 8/20 0.34
SLC1A2 P43004 1/20 0.34
HTR7 P34969 3/20 0.32
ADORA3 P0DMS8 1/20 0.31
ADORA2A P29274 1/20 0.31
ADORA1 P30542 1/20 0.31
PTPN1 P18031 1/20 0.31
BACE1 P56817 1/20 0.30

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
SCHEMBL7446685 1.00 SLC1A1 (0.38) SLC1A1LTA4HSLC1A2HTR7ADORA3
SCHEMBL9041532 0.89 LTA4H (0.32) LTA4HADORA3ADORA2AADORA1PTPN1
SCHEMBL7444849 0.86 CARM1 (0.36) ADORA3ADORA2AADORA1PTPN1BACE1
SCHEMBL7444847 0.86 CARM1 (0.36) ADORA3ADORA2AADORA1PTPN1BACE1
SCHEMBL7443351 0.85 ADORA3 (0.36) ADORA3ADORA2AADORA1PTPN1BACE1
SCHEMBL7544146 0.84 CTSC (0.34)
SCHEMBL7544144 0.84 CTSC (0.34)
Hydrochloric Acid SCHEMBL8829320 0.81 MASP2 (0.33)
SCHEMBL7446408 0.81 DRD2 (0.35) ADORA3ADORA2AADORA1PTPN1
Hydrochloric Acid SCHEMBL7447474 0.80 DRD2 (0.35) ADORA3ADORA2AADORA1PTPN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0474767-B1 DOPAMINE AGONISTS ABBOTT LAB (US) 1996-02-21 EP claimed
EP-0474767-A4 DOPAMINE AGONISTS 1992-07-08 EP claimed
EP-0474767-A1 DOPAMINE AGONISTS. ABBOTT LAB (US) 1992-03-18 EP claimed
WO-1990015056-A1 DOPAMINE AGONISTS ABBOTT LABORATORIES (US) 1990-12-13 WO claimed
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