Tipifarnib

Tipifarnib

SCHEMBL21544535

Cn1cncc1[C@@](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 SCHEMBL94807 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 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 108 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12553027-B2 Generation and cryopreservation of pluripotent stem cell-derived clinical grade corneal endothelial cells THE JOHNS HOPKINS UNIVERSITY (US) 2026-02-17 US disclosed
US-20250262211-A1 COMBINATION OF RAS INHIBITORS AND FARNESYLTRANSFERASE INHIBITORS FOR THE TREATMENT OF CANCERS INSTITUT CLAUDIUS REGAUD (FR) 2025-08-21 US disclosed
US-20250243202-A1 Compounds Useful as RET Inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2025-07-31 US disclosed
WO-2025136811-A1 CHEMICAL COMPOUNDS AND USES THEREOF IDEAYA BIOSCIENCES, INC. (US) 2025-06-26 WO disclosed
EP-4514356-A1 COMBINATION OF RAS INHIBITORS AND FARNESYLTRANSFERASE INHIBITORS FOR THE TREATMENT OF CANCERS Institut National de la Santé et de la Recherche Médicale (FR) 2025-03-05 EP disclosed
CN-119562945-A IKK inhibitors 癌症研究技术有限公司 2025-03-04 CN disclosed
US-20250059178-A1 N-(PYRIDIN-2-YL)-4-(THIAZOL-5-YL)PYRIMIDIN-2-AMINE DERIVATIVES AS THERAPEUTIC COMPOUNDS Aucentra Thereapeutics Pty LTD (AU) 2025-02-20 US disclosed
EP-4504192-A1 METHODS OF TREATING HEAD AND NECK SQUAMOUS CELL CARCINOMA Kura Oncology, Inc. (US) 2025-02-12 EP disclosed
CN-119053604-A Heterocyclic compounds for the treatment of ERK5 mediated diseases 癌症研究技术有限公司 2024-11-29 CN disclosed
EP-3708166-B1 THERAPEUTIC AGENT FOR MENTAL RETARDATION OR AUTISM TOKYO METROPOLITAN INST MEDICAL SCIENCE (JP) 2024-11-06 EP disclosed
US-7456287-B2 Diastereoselective synthesis process for the preparation of imidazole compounds JANSSEN PHARMACEUTICA N.V. (BE) 2008-11-25 US disclosed
US-7452901-B2 Anti-cancer phosphonate analogs GILEAD SCIENCES, INC. (US) 2008-11-18 US disclosed
US-7452901-B2 Anti-cancer phosphonate analogs GILEAD SCIENCES, INC. (US) 2008-11-18 US disclosed
EP-1758885-B1 DIASTEREOSELECTIVE ADDITION OF LITHIATED N-METHYLIMIDAZOLE ON SULFINIMINES JANSSEN PHARMACEUTICA NV (BE) 2008-06-18 EP disclosed
US-20070293679-A1 Diastereoselective Addition of Lithiated N-Methylimidazole on Sulfinimines JANSSEN PHARMACEUTICA N.V. (BE) 2007-12-20 US disclosed
US-20070293680-A1 For the preparation of (R)-(+)-6-[amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl) methyl]-4-(3-chlorophenyl)-1-methyl2(1H)-quinolinone; farnesyl tranferase inhibitory activity JANSSEN PHARMACEUTICA N.V. (BE) 2007-12-20 US disclosed
US-20070293679-A1 Diastereoselective Addition of Lithiated N-Methylimidazole on Sulfinimines JANSSEN PHARMACEUTICA N.V. (BE) 2007-12-20 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-20070093449-A1 Novel IV formulation of tipifarnib JANSSEN PHARMACEUTICA, N.V. (BE) 2007-04-26 US disclosed
US-20070093449-A1 Novel IV formulation of tipifarnib JANSSEN PHARMACEUTICA, N.V. (BE) 2007-04-26 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 (8 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-20250059178-A1 N-(PYRIDIN-2-YL)-4-(THIAZOL-5-YL)PYRIMIDIN-2-AMINE DERIVATIVES AS THERAPEUTIC COMPOUNDS CDK4, CDK6, CDK2 FNTA 4379/4885FNTB 4047/4885CYP3A4 2471/4885
US-20250243202-A1 Compounds Useful as RET Inhibitors RET, BCR, REL FNTA 4507/4885FNTB 3379/4885CYP3A4 3158/4885
US-12553027-B2 Generation and cryopreservation of pluripotent stem cell-derived clinical grade corneal endothelial cells CD14, NGF, NEFM FNTA 2180/4885FNTB 2553/4885CYP3A4 3263/4885
US-20070293680-A1 For the preparation of (R)-(+)-6-[amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl) methyl]-4-(3-chlorophenyl)-1-methyl2(1H)-quinolinone; farnesyl tranferase inhibitory activity FNTB, CYP4F2, FNTA FNTA 3/4885FNTB 1/4885CYP3A4 496/4885
US-20070093449-A1 Novel IV formulation of tipifarnib FLT4, F5, FLT1 FNTA 280/4885FNTB 699/4885CYP3A4 638/4885
US-20070238880-A1 Diastereoselective Synthesis Process for the Preparation of Imidazole Compounds DHPS, CYP2S1, CYP1A2 FNTA 1134/4885FNTB 1198/4885CYP3A4 17/4885
US-20250262211-A1 COMBINATION OF RAS INHIBITORS AND FARNESYLTRANSFERASE INHIBITORS FOR THE TREATMENT OF CANCERS KRAS, FNTA, NRAS FNTA 2/4885FNTB 4/4885CYP3A4 2819/4885
US-20070293679-A1 Diastereoselective Addition of Lithiated N-Methylimidazole on Sulfinimines SULT1A1, SULT1E1, CSNK1A1L FNTA 4242/4885FNTB 3766/4885CYP3A4 97/4885

“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.