Tipifarnib

Tipifarnib

SCHEMBL94807

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

nearest known ligand 0.80

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

FNTAFNTB

The experimentally established mechanism targets of Tipifarnib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
FNTA known ✓ P49354 15/20 0.80
FNTB known ✓ P49356 15/20 0.80
CYP3A4 P08684 5/20 0.76
PGGT1B P53609 3/20 0.71

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
Tipifarnib SCHEMBL22772860 1.00 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
(S)-Tipifarnib SCHEMBL30436988 1.00 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
Tipifarnib SCHEMBL29371885 1.00 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
Tipifarnib SCHEMBL8097 1.00 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
Tipifarnib SCHEMBL29352433 1.00 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
Tipifarnib SCHEMBL23633189 1.00 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
(S)-Tipifarnib SCHEMBL4429738 1.00 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
Tipifarnib SCHEMBL21544535 1.00 FNTA (0.80) FNTAFNTBCYP3A4PGGT1B
Tipifarnib SCHEMBL22468601 0.96 FNTA (0.74) FNTAFNTBCYP3A4PGGT1B
SCHEMBL12021666 0.95 FNTA (0.72) 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 977 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220249504-A1 LONGEVITY SIGNATURES AND THEIR APPLICATIONS THE BRIGHAM AND WOMEN'S HOSPITAL, INC. 2022-08-11 US claimed
WO-2021007551-A1 LONGEVITY SIGNATURES AND THEIR APPLICATIONS THE BRIGHAM AND WOMEN'S HOSPITAL, INC. (US) 2021-01-14 WO claimed
EP-1931677-B1 NOVEL PYRAZOLOPYRIMIDINES AS CYCLIN DEPENDENT KINASE INHIBITORS MERCK SHARP & DOHME (US) 2016-04-20 EP claimed
WO-2015194710-A1 COMPOSITION COMPRISING MESENCHYMAL STEM CELLS TREATED WITH STAT3 INHIBITOR AS ACTIVE INGREDIENT FOR PREVENTING OR TREATING IMMUNE DISEASES 가톨릭대학교 산학협력단 2015-12-23 WO claimed
US-20140301976-A1 NOVEL HYDROXAMATES AS THERAPEUTIC AGENTS PHARMACYCLICS, INC. 2014-10-09 US claimed
EP-2362218-B1 METHODS OF MONITORING THE EFFICACY OF FARNESYLTRANSFERASE INHIBITORS JANSSEN PHARMACEUTICA NV (BE) 2014-08-27 EP claimed
US-8779171-B2 Hydroxamates as therapeutic agents PHARMACYCLICS, INC. (US) 2014-07-15 US claimed
US-20130303564-A1 METHOD FOR TREATING A NEURODEGENERATIVE DISORDER RUSH UNIVERSITY MEDICAL CENTER 2013-11-14 US claimed
US-8557847-B2 Synergistic modulation of FLT3 kinase using a FLT3 inhibitor and a farnesyl transferase inhibitor JANSSEN PHARMACEUTICA, N.V. (BE) 2013-10-15 US claimed
US-20130142758-A1 NOVEL HYDROXAMATES AS THERAPEUTIC AGENTS PHARMACYCLICS, INC. (US) 2013-06-06 US claimed
EP-1094839-A1 FARNESYL PROTEIN TRANSFERASE INHIBITORS WITH $i(IN VIVO) RADIOSENSITIZING PROPERTIES JANSSEN PHARMACEUTICA N.V. (BE) 2001-05-02 EP claimed
EP-1094815-A1 FARNESYL PROTEIN TRANSFERASE INHIBITORS FOR TREATING ARTHROPATHIES Janssen Pharmaceutica N.V. (BE) 2001-05-02 EP claimed
WO-2000025789-A1 A METHOD OF TREATING ENDOMETRIOSIS MERCK & CO., INC. (US) 2000-05-11 WO claimed
EP-0988038-A1 (IMIDAZOL-5-YL)METHYL-2-QUINOLINONE DERIVATIVES AS INHIBITORS OF SMOOTH MUSCLE CELL PROLIFERATION JANSSEN PHARMACEUTICA N.V. (BE) 2000-03-29 EP claimed
US-6037350-A USEFUL AS ANTICANCER AGENTS FOR TUMORS JANSSEN PHARMACEUTICA, N.V. (BE) 2000-03-14 US claimed
WO-2000001386-A1 FARNESYL PROTEIN TRANSFERASE INHIBITORS FOR TREATING ARTHROPATHIES JANSSEN PHARMACEUTICA N.V. (BE) 2000-01-13 WO claimed
WO-2000001411-A1 FARNESYL PROTEIN TRANSFERASE INHIBITORS WITH IN VIVO RADIOSENSITIZING PROPERTIES JANSSEN PHARMACEUTICA N.V. (BE) 2000-01-13 WO claimed
WO-1998055124-A1 (IMIDAZOL-5-YL)METHYL-2-QUINOLINONE DERIVATIVES AS INHIBITORS OF SMOOTH MUSCLE CELL PROLIFERATION JANSSEN PHARMACEUTICA N.V. (BE) 1998-12-10 WO claimed
EP-0865440-A1 FARNESYL PROTEIN TRANSFERASE INHIBITING (IMIDAZOL-5-YL)METHYL-2-QUINOLINONE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 1998-09-23 EP claimed
WO-1997021701-A1 FARNESYL PROTEIN TRANSFERASE INHIBITING (IMIDAZOL-5-YL)METHYL-2-QUINOLINONE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 1997-06-19 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 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-20130142758-A1 NOVEL HYDROXAMATES AS THERAPEUTIC AGENTS HDAC1, HDAC3, HDAC5 FNTA 3317/4885FNTB 1753/4885CYP3A4 3651/4885
US-20140301976-A1 NOVEL HYDROXAMATES AS THERAPEUTIC AGENTS HDAC1, HDAC3, HDAC5 FNTA 3317/4885FNTB 1753/4885CYP3A4 3651/4885
US-20220249504-A1 LONGEVITY SIGNATURES AND THEIR APPLICATIONS GLA, LIMS1, GLB1 FNTA 2042/4885FNTB 3483/4885CYP3A4 4869/4885

“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.