SCHEMBL4373285

SCHEMBL4373285

Cc1ccccc1-c1cc(N2CCSCC2)ncc1N(C)C(=O)C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1

nearest known ligand 0.82

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
TACR1 P25103 19/20 0.82
CYP3A4 P08684 4/20 0.74
TACR3 P29371 6/20 0.63
GPBAR1 Q8TDU6 1/20 0.61

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
Netupitant SCHEMBL445804 0.90 TACR1 (1.00) TACR1CYP3A4TACR3GPBAR1
Netupitant SCHEMBL29809811 0.90 TACR1 (1.00) TACR1CYP3A4TACR3GPBAR1
SCHEMBL4375262 0.90 TACR1 (0.78) TACR1CYP3A4TACR3
Netupitant SCHEMBL17222804 0.90 TACR1 (0.98) TACR1CYP3A4TACR3GPBAR1
Befetupitant SCHEMBL29374667 0.90 TACR1 (1.00) TACR1CYP3A4TACR3GPBAR1
Befetupitant SCHEMBL1399438 0.90 TACR1 (1.00) TACR1CYP3A4TACR3GPBAR1
Netupitant SCHEMBL6637560 0.90 TACR1 (0.98) TACR1CYP3A4TACR3GPBAR1
SCHEMBL1399508 0.90 TACR1 (0.82) TACR1CYP3A4TACR3GPBAR1
Netupitant SCHEMBL30800106 0.90 TACR1 (0.98) TACR1CYP3A4TACR3GPBAR1
SCHEMBL5966367 0.89 TACR1 (1.00) TACR1CYP3A4TACR3GPBAR1

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
EP-1414525-B1 2-(3,5-BIS-TRIFLUOROMETHYL-PHENYL)-N-¬6-(1,1-DIOXO-1.LAMBDA.6-THIOMORPHOLIN-4-YL)-4-(2-METHYL OR 4-FLUORO-2-METHYL SUBSTITUTED)PHENYL-PYRIDIN-3-YL -N-METHYL-ISOBUTYRAMIDE HOFFMANN LA ROCHE (CH) 2009-05-06 EP disclosed
EP-1385577-B1 USE OF NK-1 RECEPTOR ANTAGONISTS AGAINST BENIGN PROSTATIC HYPERPLASIA HOFFMANN LA ROCHE (CH) 2006-04-19 EP disclosed
US-6849624-B2 Aromatic and heteroaromatic substituted amides HOFFMANN-LA ROCHE INC. (US) 2005-02-01 US disclosed
EP-1414525-A2 2-(3,5-BIS-TRIFLUOROMETHYL-PHENYL)-N-[6-(1,1-DIOXO-1.LAMBDA.6-THIOMORPHOLIN-4-YL)-4-(2-METHYL OR 4-FLUORO-2-METHYL SUBSTITUTED)PHENYL-PYRIDIN-3-YL]-N-METHYL-ISOBUTYRAMIDE F. HOFFMANN-LA ROCHE AG (CH) 2004-05-06 EP disclosed
EP-1385577-A2 USE OF NK-1 RECEPTOR ANTAGONISTS AGAINST BENIGN PROSTATIC HYPERPLASIA F. Hoffman-la Roche AG (CH) 2004-02-04 EP disclosed
US-20030064983-A1 Aromatic and heteroaromatic substituted amides F. HOFFMANN-LA ROCHE AG, A SWISS COMPANY (CH) 2003-04-03 US disclosed
WO-2003011860-A2 2-(3,5-BIS-TRIFLUOROMETHYL-PHENYL)-N-[6-(1,1-DIOXO-1λ6-THIOMORPHOLIN-4-YL)-4-(2-METHYL OR 4-FLUORO-2-METHYL SUBSTITUTED)PHENYL-PYRIDIN-3-YL]-N-METHYL-ISOBUTYRAMIDE F. HOFFMANN-LA ROCHE AG (CH) 2003-02-13 WO disclosed
US-20030004157-A1 Use of NK-1 receptor antagonists against benign prostatic hyperplasia F. HOFFMANN-LA ROCHE AG (CH) 2003-01-02 US disclosed
WO-2002085458-A2 USE OF NK-1 RECEPTOR ANTAGONISTS AGAINST BENIGN PROSTATIC HYPERPLASIA F. HOFFMAN-LA ROCHE AG (CH) 2002-10-31 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-20030064983-A1 Aromatic and heteroaromatic substituted amides OPRK1, HRH4, OPRL1 TACR1 199/4885CYP3A4 353/4885TACR3 871/4885
US-20030004157-A1 Use of NK-1 receptor antagonists against benign prostatic hyperplasia KLK3, TACR1, TACR2 TACR1 2/4885CYP3A4 1133/4885TACR3 124/4885

“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.