SCHEMBL5800713

SCHEMBL5800713

O=C(c1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCC(N2CCNCC2)C(c2ccccc2)C1

nearest known ligand 0.47

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
SLC18A3 Q16572 1/20 0.47
TACR1 P25103 7/20 0.46
RHOA P61586 4/20 0.44
RHOC P08134 2/20 0.44
CYP3A4 P08684 2/20 0.43
TSHR P16473 1/20 0.43
USP2 O75604 2/20 0.43
HSD17B10 Q99714 1/20 0.43
NPC1 O15118 1/20 0.42
RAB9A P51151 1/20 0.42
ATM Q13315 1/20 0.42

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
SCHEMBL5918111 1.00 SLC18A3 (0.47) SLC18A3TACR1RHOARHOCCYP3A4
SCHEMBL5918155 0.91 HSD11B1 (0.44) SLC18A3TACR1RHOARHOCNPC1
SCHEMBL5918154 0.91 HSD11B1 (0.44) SLC18A3TACR1RHOARHOCNPC1
SCHEMBL6441487 0.91 RHOA (0.49) SLC18A3TACR1RHOARHOCCYP3A4
SCHEMBL6441492 0.91 RHOA (0.49) SLC18A3TACR1RHOARHOCCYP3A4
SCHEMBL6443352 0.89 SLC18A3 (0.50) SLC18A3TACR1RHOARHOCCYP3A4
SCHEMBL6440261 0.89 RHOA (0.45) SLC18A3TACR1RHOARHOCCYP3A4
SCHEMBL5817146 0.89 SLC18A3 (0.50) SLC18A3TACR1RHOARHOCCYP3A4
SCHEMBL5803605 0.89 CYP3A4 (0.47) SLC18A3TACR1RHOARHOCCYP3A4
SCHEMBL5918246 0.89 CYP3A4 (0.47) SLC18A3TACR1RHOARHOCCYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1360184-B1 PIPERIDINE DERIVATIVES AS NEUROKININ 1 ANTAGONISTS HOFFMANN LA ROCHE (CH) 2005-03-30 EP claimed
EP-1360184-A1 PIPERIDINEE DERIVATIVES AS NEUROKININ 1 ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2003-11-12 EP claimed
US-6642226-B2 Such as cis-(3,5-bis-trifluoromethyl-phenyl)-(4-(4-methyl-piperazin-1-yl),-3-phenyl -piperidin-1-yl)-methanone; for treatment of diseases related to neurokinin receptors HOFFMAN-LA ROCHE INC. 2003-11-04 US claimed
US-20020151547-A1 Substituted phenyl-piperidine methanone compounds F.HOFFMANN-LA ROCHE AG (CH) 2002-10-17 US claimed
WO-2002062784-A1 PIPERIDINEE DERIVATIVES AS NEUROKININ 1 ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2002-08-15 WO claimed
US-20060178348-A1 Compositions and therapeutic methods utilizing a combination of a protein extravasation inhibitor and an NSAID POZEN INC. (US) 2006-08-10 US disclosed
WO-2006081088-A2 COMPOSITIONS AND THERAPEUTIC METHODS UTILIZING A COMBINATION OF A PROTEIN EXTRAVASATION INHIBITOR AND AN NSAID POZEN INC. (US) 2006-08-03 WO disclosed
EP-1360184-B1 PIPERIDINE DERIVATIVES AS NEUROKININ 1 ANTAGONISTS HOFFMANN LA ROCHE (CH) 2005-03-30 EP disclosed
EP-1360184-A1 PIPERIDINEE DERIVATIVES AS NEUROKININ 1 ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2003-11-12 EP disclosed
US-6642226-B2 Such as cis-(3,5-bis-trifluoromethyl-phenyl)-(4-(4-methyl-piperazin-1-yl),-3-phenyl -piperidin-1-yl)-methanone; for treatment of diseases related to neurokinin receptors HOFFMAN-LA ROCHE INC. 2003-11-04 US disclosed
US-20020151547-A1 Substituted phenyl-piperidine methanone compounds F.HOFFMANN-LA ROCHE AG (CH) 2002-10-17 US disclosed
WO-2002062784-A1 PIPERIDINEE DERIVATIVES AS NEUROKININ 1 ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2002-08-15 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 (2 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-20060178348-A1 Compositions and therapeutic methods utilizing a combination of a protein extravasation inhibitor and an NSAID MMP8, CCL2, VCAM1 SLC18A3 352/4885TACR1 240/4885RHOA 278/4885
US-20020151547-A1 Substituted phenyl-piperidine methanone compounds TACR1, OPRK1, TACR2 SLC18A3 2396/4885TACR1 1/4885RHOA 4345/4885

“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.