SCHEMBL3365490

SCHEMBL3365490

Cn1cncc1C(Cl)(c1ccc(Cl)cc1)c1ccc2c(c1)c(-c1cccc(Cl)c1)cc(=O)n2C

nearest known ligand 0.80

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
FNTA P49354 12/20 0.80
FNTB P49356 12/20 0.80
CYP3A4 P08684 8/20 0.65
PGGT1B P53609 2/20 0.58

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
SCHEMBL5656156 0.91 FNTA (0.68) FNTAFNTBCYP3A4PGGT1B
Hydrochloric Acid SCHEMBL5658016 0.90 FNTA (0.66) FNTAFNTBCYP3A4PGGT1B
SCHEMBL6010453 0.90 FNTA (0.68) FNTAFNTBCYP3A4PGGT1B
Tipifarnib SCHEMBL8097 0.89 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
Tipifarnib SCHEMBL22772860 0.89 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
Tipifarnib SCHEMBL23633189 0.89 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
(S)-Tipifarnib SCHEMBL4429738 0.89 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
Tipifarnib SCHEMBL21544535 0.89 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
SCHEMBL11947168 0.89 FNTA (1.00) FNTAFNTBCYP3A4PGGT1B
SCHEMBL6843800 0.89 FNTA (1.00) FNTAFNTBCYP3A4PGGT1B

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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11542244-B2 Synthesis of tipifarnib KURA ONCOLOGY, INC. (US) 2023-01-03 US disclosed
US-20210246114-A1 SYNTHESIS OF TIPIFARNIB KURA ONCOLOGY, INC. (US) 2021-08-12 US disclosed
EP-1756085-B1 DIASTEREOSELECTIVE SYNTHESIS PROCESS WITH 6-BROMO-4-(3-CHLOROPHENYL)-2-METHOXY-QUINOLINE JANSSEN PHARMACEUTICA NV (BE) 2010-06-16 EP disclosed
US-7572916-B2 Diastereoselective synthesis process with 6-bromo-4-(3-chlorophenyl)-2-methoxy-quinoline JANSSEN PHARMACEUTICA NV (BE) 2009-08-11 US disclosed
US-7572916-B2 Diastereoselective synthesis process with 6-bromo-4-(3-chlorophenyl)-2-methoxy-quinoline JANSSEN PHARMACEUTICA NV (BE) 2009-08-11 US disclosed
US-7524961-B2 Diastereoselective addition of lithiated N-methylimidazole on sulfinimines JANSSEN PHARMACEUTICA, N.V. (BE) 2009-04-28 US disclosed
US-7524961-B2 Diastereoselective addition of lithiated N-methylimidazole on sulfinimines JANSSEN PHARMACEUTICA, N.V. (BE) 2009-04-28 US disclosed
US-7524961-B2 Diastereoselective addition of lithiated N-methylimidazole on sulfinimines JANSSEN PHARMACEUTICA, N.V. (BE) 2009-04-28 US disclosed
US-7456287-B2 Diastereoselective synthesis process for the preparation of imidazole compounds JANSSEN PHARMACEUTICA N.V. (BE) 2008-11-25 US disclosed
US-7456287-B2 Diastereoselective synthesis process for the preparation of imidazole compounds JANSSEN PHARMACEUTICA N.V. (BE) 2008-11-25 US disclosed
US-20070238880-A1 Diastereoselective Synthesis Process for the Preparation of Imidazole Compounds JANSSEN PHARMACEUTICA N.V. (BE) 2007-10-11 US disclosed
US-20070238880-A1 Diastereoselective Synthesis Process for the Preparation of Imidazole Compounds JANSSEN PHARMACEUTICA N.V. (BE) 2007-10-11 US disclosed
US-20070238880-A1 Diastereoselective Synthesis Process for the Preparation of Imidazole Compounds JANSSEN PHARMACEUTICA N.V. (BE) 2007-10-11 US disclosed
EP-1756085-A1 DIASTEREOSELECTIVE SYNTHESIS PROCESS WITH 6-BROMO-4-(3-CHLOROPHENYL)-2-METHOXY-QUINOLINE JANSSEN PHARMACEUTICA N.V. (BE) 2007-02-28 EP disclosed
WO-2005105783-A1 DIASTEREOSELECTIVE SYNTHESIS PROCESS WITH 6-BROMO-4-(3-CHLOROPHENYL)-2-METHOXY-QUINOLINE JANSSEN PHARMACEUTICA N.V. (BE) 2005-11-10 WO disclosed
EP-1373255-B1 PROCESS FOR THE PREPARATION OF IMIDAZOLE COMPOUNDS JANSSEN PHARMACEUTICA NV (BE) 2005-01-26 EP disclosed
US-6844439-B2 Process for the preparation of imidazole compounds JANSEN PHARMACEUTICA, NV (BE) 2005-01-18 US disclosed
US-20040138256-A1 Process for the preparation of imidazole compounds JANSSEN PHARMACEUTICA N.V. (BE) 2004-07-15 US disclosed
EP-1373255-A1 PROCESS FOR THE PREPARATION OF IMIDAZOLE COMPOUNDS JANSSEN PHARMACEUTICA N.V. (BE) 2004-01-02 EP disclosed
WO-2002072574-A1 PROCESS FOR THE PREPARATION OF IMIDAZOLE COMPOUNDS JANSSEN PHARMACEUTICA N.V. (BE) 2002-09-19 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 (4 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-20210246114-A1 SYNTHESIS OF TIPIFARNIB TIPARP, RTF1, TTBK1 FNTA 1300/4885FNTB 754/4885CYP3A4 1391/4885
US-20040138256-A1 Process for the preparation of imidazole compounds AZI2, DOT1L, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16 FNTA 3238/4885FNTB 3264/4885CYP3A4 14/4885
US-11542244-B2 Synthesis of tipifarnib TIPARP, RTF1, TTBK1 FNTA 1300/4885FNTB 754/4885CYP3A4 1391/4885
US-20070238880-A1 Diastereoselective Synthesis Process for the Preparation of Imidazole Compounds DHPS, CYP2S1, CYP1A2 FNTA 1134/4885FNTB 1198/4885CYP3A4 17/4885

“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.