SCHEMBL4979313

SCHEMBL4979313

COc1ccc2c(OC3CC(C(=O)NC4(C(=O)O)CC45CC5)N(C(=O)C(NC(=O)OC(C)(C)C)C(C)(C)C)C3)cc(-c3ccccc3)nc2c1

nearest known ligand 0.50

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 2/20 0.47
CTSB P07858 1/20 0.41
PPP3CB P16298 1/20 0.41
ELANE P08246 11/20 0.41
ABCC1 P33527 1/20 0.37
ABCC2 Q92887 1/20 0.37
ABCG2 Q9UNQ0 1/20 0.37
KDM4E B2RXH2 1/20 0.37
ALDH1A1 P00352 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.37
TACR3 P29371 1/20 0.36

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
SCHEMBL8354091 1.00 CYP3A4 (0.47) CYP3A4CTSBPPP3CBELANEABCC1
SCHEMBL5692578 0.98 CYP3A4 (0.46) CYP3A4CTSBPPP3CBELANEABCC1
SCHEMBL5692629 0.93 CYP3A4 (0.46) CYP3A4CTSBPPP3CBELANEABCC1
SCHEMBL5692632 0.92 CYP3A4 (0.58) CYP3A4CTSB
SCHEMBL8353025 0.92 CYP3A4 (0.50) CYP3A4CTSBPPP3CBELANEABCC1
SCHEMBL5692664 0.91 CYP3A4 (0.49) CYP3A4CTSBPPP3CBELANEABCC1
SCHEMBL12891920 0.91 CYP3A4 (0.49) CYP3A4CTSBPPP3CBELANEABCC1
SCHEMBL8354706 0.90 CYP3A4 (0.48) CYP3A4CTSBPPP3CBELANEABCC1
SCHEMBL6308074 0.90 CYP3A4 (0.57) CYP3A4CTSB
SCHEMBL5693284 0.90 CYP3A4 (0.57) CYP3A4CTSB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1505945-B1 SUBSTITUTED CYCLOALKYL P1' HEPATITIS C VIRUS INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2008-11-05 EP disclosed
EP-1505945-A4 SUBSTITUTED CYCLOALKYL P1' HEPATITIS C VIRUS INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2006-11-22 EP disclosed
US-6878722-B2 Substituted cycloalkyl P1′ hepatitis C virus inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2005-04-12 US disclosed
EP-1505945-A2 SUBSTITUTED CYCLOALKYL P1' HEPATITIS C VIRUS INHIBITORS Bristol-Myers Squibb Pharma Company (US) 2005-02-16 EP disclosed
WO-2004043339-A2 SUBSTITUTED CYCLOALKYL P1' HEPATITIS C VIRUS INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2004-05-27 WO disclosed
US-20040077551-A1 Substituted cycloalkyl P1' hepatitis C virus inhibitors BRISTOL-MYERS SQUIBB COMPANY 2004-04-22 US 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-20040077551-A1 Substituted cycloalkyl P1' hepatitis C virus inhibitors HAVCR2, ANPEP, ENPEP CYP3A4 2730/4885CTSB 203/4885PPP3CB 214/4885

“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.