SCHEMBL12588136

SCHEMBL12588136

O=C1NC(=O)[C@]2(CC[C@H](c3ccc(Br)cc3)C2)N1

nearest known ligand 0.47

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
PDE7A Q13946 4/20 0.40
LIG1 P18858 1/20 0.38
BRD4 O60885 1/20 0.35
MMP13 P45452 1/20 0.35
AKR1A1 P14550 3/20 0.34
AKR1B1 P15121 3/20 0.34
CRBN Q96SW2 2/20 0.33
IDO1 P14902 1/20 0.33
TDO2 P48775 1/20 0.33
DDB1 Q16531 1/20 0.32

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
SCHEMBL10299843 1.00 PDE7A (0.40) PDE7ALIG1BRD4MMP13AKR1A1
SCHEMBL12588138 1.00 PDE7A (0.40) PDE7ALIG1BRD4MMP13AKR1A1
SCHEMBL15954215 1.00 PDE7A (0.40) PDE7ALIG1BRD4MMP13AKR1A1
SCHEMBL2046597 1.00 PDE7A (0.40) PDE7ALIG1BRD4MMP13AKR1A1
SCHEMBL14144951 1.00 PDE7A (0.40) PDE7ALIG1BRD4MMP13AKR1A1
SCHEMBL2046599 1.00 PDE7A (0.40) PDE7ALIG1BRD4MMP13AKR1A1
SCHEMBL18052662 0.86 PDE7A (0.39) PDE7ALIG1BRD4
SCHEMBL12588137 0.86 LIG1 (0.36) PDE7ALIG1BRD4
SCHEMBL7070786 0.85 CRBN (0.43) PDE7AAKR1A1AKR1B1CRBNDDB1
SCHEMBL2047677 0.77 BRD4 (0.42) PDE7ALIG1BRD4

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-7956195-B2 reacting arylboronic acids with a cycloalkanone, in the presence of a rhodium catalyst or BINAP, to form a substituted arylcycloalkanone, then formin of a hydantoin, alkylation of the hydantoin, resolution, hydrolysis of the hydantoin to the amino acids and esterification of acids; chemical intermediates ABBOTT LABORATORIES (US) 2011-06-07 US disclosed
US-7956195-B2 reacting arylboronic acids with a cycloalkanone, in the presence of a rhodium catalyst or BINAP, to form a substituted arylcycloalkanone, then formin of a hydantoin, alkylation of the hydantoin, resolution, hydrolysis of the hydantoin to the amino acids and esterification of acids; chemical intermediates ABBOTT LABORATORIES (US) 2011-06-07 US disclosed
US-20080255367-A1 Process for the preparation and isolation of the individual stereoisomers of 1-amino, 3-substituted phenylcyclopentane-carboxylates ABBVIE INC. 2008-10-16 US disclosed
US-20080255367-A1 Process for the preparation and isolation of the individual stereoisomers of 1-amino, 3-substituted phenylcyclopentane-carboxylates ABBVIE INC. 2008-10-16 US disclosed
WO-2008079380-A1 PROCESS FOR THE PREPARATION AND ISOLATION OF THE INDIVIDUAL STEREOISOMERS OF 1-AMINO, 3-SUBSTITUTED PHENYLCYCLOPENTANE CARBOXYLATES ABBOTT LABORATORIES (US) 2008-07-03 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 (1 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-20080255367-A1 Process for the preparation and isolation of the individual stereoisomers of 1-amino, 3-substituted phenylcyclopentane-carboxylates DDC, DNPEP, AAAS PDE7A 1833/4885LIG1 340/4885BRD4 2791/4885

“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.