SCHEMBL5864478

SCHEMBL5864478

O=C1c2ccccc2C(=O)N1CCc1nc2ccccc2[nH]1

nearest known ligand 0.64

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.64
PDE10A Q9Y233 3/20 0.59
POLB P06746 1/20 0.57
EGLN3 Q9H6Z9 2/20 0.55
NPC1 O15118 2/20 0.53
RAB9A P51151 2/20 0.53
CHRM1 P11229 1/20 0.52
DRD4 P21917 1/20 0.50
CYP2D6 P10635 1/20 0.49
CYP2C19 P33261 1/20 0.49
CHRNA7 P36544 1/20 0.49
MEN1 O00255 1/20 0.49
GAA P10253 1/20 0.49
MAPT P10636 1/20 0.49
KMT2A Q03164 1/20 0.49

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
SCHEMBL12202119 0.92 ALDH1A1 (0.68) ALDH1A1PDE10APOLBNPC1RAB9A
SCHEMBL14332366 0.82 ALDH1A1 (0.86) ALDH1A1GAAMAPT
SCHEMBL4788011 0.80 ALDH1A1 (0.62) ALDH1A1PDE10A
SCHEMBL17525710 0.80 POLB (0.54) PDE10APOLBEGLN3NPC1RAB9A
SCHEMBL7475210 0.80 PDE10A (0.48) ALDH1A1PDE10APOLBNPC1RAB9A
SCHEMBL8327859 0.79 ALDH1A1 (0.64) ALDH1A1
SCHEMBL230157 0.77 POLB (0.84) PDE10APOLBNPC1RAB9ACHRM1
SCHEMBL1115713 0.77 ALDH1A1 (0.55) ALDH1A1PDE10APOLBCYP2D6CYP2C19
SCHEMBL7479144 0.76 GAA (0.46) ALDH1A1PDE10ANPC1RAB9AMEN1
SCHEMBL5509427 0.74 PDE10A (0.84) ALDH1A1PDE10APOLBNPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6984642-B1 Substituted phenylcyclohexane carboxylic acid amides and their use as adenosine uptake inhibitors BAYER AKTIENGESELLSCHAFT (DE) 2006-01-10 US disclosed
EP-1187812-B1 SUBSTITUTED PHENYLCYCLOHEXANE CARBOXYLIC ACID AMIDES AND THEIR USE AS ADENOSINE UPTAKE INHIBITORS BAYER HEALTHCARE AG (DE) 2005-09-07 EP disclosed
US-20040186106-A1 Substituted phenylcyclohexane carboxylic acid amides that have an adenosine uptake inhibiting effect BAYER HEALTHCARE AG (DE) 2004-09-23 US disclosed
US-6716849-B1 ISCHEMIC BRAIN DISORDERS; NEUROPROTECTANTS BAYER AKTIENGESELLSCHAFT (DE) 2004-04-06 US disclosed
EP-1185516-B1 SUBSTITUTED PHENYLCYCLOHEXANE CARBOXYLIC ACID AMIDES THAT HAVE AN ADENOSINE UPTAKE INHIBITING EFFECT BAYER AG (DE) 2003-05-02 EP disclosed
EP-1187812-A2 SUBSTITUTED PHENYLCYCLOHEXANE CARBOXYLIC ACID AMIDES AND THEIR USE AS ADENOSINE UPTAKE INHIBITORS Bayer Aktiengesellschaft (DE) 2002-03-20 EP disclosed
EP-1185516-A1 SUBSTITUTED PHENYLCYCLOHEXANE CARBOXYLIC ACID AMIDES THAT HAVE AN ADENOSINE UPTAKE INHIBITING EFFECT Bayer Aktiengesellschaft (DE) 2002-03-13 EP disclosed
WO-2000073274-A2 SUBSTITUTED PHENYLCYCLOHEXANE CARBOXYLIC ACID AMIDES AND THEIR USE AS ADENOSINE UPTAKE INHIBITORS BAYER AKTIENGESELLSCHAFT (DE) 2000-12-07 WO disclosed
WO-2000073275-A1 SUBSTITUTED PHENYLCYCLOHEXANE CARBOXYLIC ACID AMIDES THAT HAVE AN ADENOSINE UPTAKE INHIBITING EFFECT BAYER AKTIENGESELLSCHAFT (DE) 2000-12-07 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-20040186106-A1 Substituted phenylcyclohexane carboxylic acid amides that have an adenosine uptake inhibiting effect ADORA1, ADORA2A, ADORA3 ALDH1A1 312/4885PDE10A 403/4885POLB 1409/4885

“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.