Defactinib

Defactinib

SCHEMBL1627234

CNC(=O)c1ccc(Nc2ncc(C(F)(F)F)c(NCc3nccnc3N(C)S(C)(=O)=O)n2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTK2PTK2B

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PTK2 known ✓ Q05397 20/20 1.00
▸ PTK2B known ✓ Q14289 2/20 1.00
▸ AURKA O14965 1/20 1.00
▸ JAK2 O60674 1/20 1.00
▸ STK16 O75716 1/20 1.00
▸ CDKL5 O76039 1/20 1.00
▸ LATS1 O95835 1/20 1.00
▸ PAK4 O96013 1/20 1.00
▸ ABL1 P00519 1/20 1.00
▸ NTRK1 P04629 1/20 1.00
▸ CDK1 P06493 1/20 1.00
▸ LYN P07948 1/20 1.00
▸ RET P07949 1/20 1.00
▸ ADORA3 P0DMS8 1/20 1.00
▸ FER P16591 1/20 1.00
▸ FLT1 P17948 1/20 1.00
▸ ERCC2 P18074 1/20 1.00
▸ CSNK2A2 P19784 1/20 1.00
▸ CCNA2 P20248 1/20 1.00
▸ DRD1 P21728 1/20 1.00

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
Defactinib SCHEMBL1626017 0.99 PTK2 (0.98) PTK2PTK2BAURKAJAK2STK16
Defactinib SCHEMBL23086796 0.94 PTK2 (0.89) PTK2PTK2BAURKAJAK2STK16
Defactinib SCHEMBL28419282 0.94 PTK2 (0.89) PTK2PTK2BAURKAJAK2STK16
SCHEMBL26126341 0.92 PTK2 (0.86) PTK2PTK2BAURKAJAK2STK16
SCHEMBL31653624 0.92 PTK2 (0.86) PTK2PTK2BAURKAJAK2STK16
SCHEMBL29853474 0.91 PTK2 (1.00) PTK2PTK2BAURKAJAK2STK16
SCHEMBL1627066 0.91 PTK2 (1.00) PTK2PTK2BAURKAJAK2STK16
Defactinib SCHEMBL23086969 0.91 PTK2 (0.83) PTK2PTK2BAURKAJAK2STK16
Defactinib SCHEMBL23701664 0.91 PTK2 (0.83) PTK2PTK2BAURKAJAK2STK16
SCHEMBL1626939 0.90 PTK2 (1.00) PTK2PTK2BAURKAJAK2STK16

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 1449 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260137839-A1 CONTROLLED HYDROGEL DELIVERY OF FOCAL ADHESION KINASE INHIBITOR FOR DECREASED SCAR FORMATION THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2026-05-21 — — US claimed
EP-4096671-B1 COMBINATION THERAPY FOR TREATING ABNORMAL CELL GROWTH VERASTEM INC (US) 2026-05-06 — — EP claimed
WO-2026090321-A1 TREATMENT OF CANCER WITH A KRAS INHIBITOR ALTEROME THERAPEUTICS, INC. (US) 2026-04-30 — — WO claimed
WO-2026090174-A1 COMPOSITIONS FOR TARGETED DELIVERY OF THERAPEUTIC AGENTS AND METHODS FOR THE SYNTHESIS AND USE THEREOF BRYET US, INC. (US) 2026-04-30 — — WO claimed
EP-4028010-B1 VS-6063 IN COMBINATION WITH CH5126766 FOR THE TREATMENT OF CANCER THE INSTITUTE OF CANCER RES ROYAL CANCER HOSPITAL (GB) 2026-04-08 — — EP claimed
US-12594421-B2 Compositions and methods for increasing cancer cell sensitivity to alternating electric fields NOVOCURE GMBH (CH) 2026-04-07 — — US claimed
US-20260060936-A1 INDOLIUM-BASED STABILIZERS OF HYDROPHOBIC DRUGS TECHNION RES & DEV FOUNDATION (IL) 2026-03-05 — — US claimed
US-20260034128-A1 THERAPEUTIC COMPOSITIONS, COMBINATIONS, AND METHODS OF USE THE INSTITUTE OF CANCER RES ROYAL CANCER HOSPITAL (GB) 2026-02-05 — — US claimed
US-12521394-B2 Therapeutic compositions and methods for treating cancers Pattern Computer, Inc. (US) 2026-01-13 — — US claimed
EP-3999065-B1 THERAPEUTIC COMPOSITIONS COMPRISING IDELALISIB AND DEFACTINIB FOR TREATING BREAST CANCERS PATTERN COMPUTER INC (US) 2025-12-24 — — EP claimed
EP-3957631-A1 QUINOLINE COMPOUND OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF FOR TREATING EWING'S SARCOMA Chia Tai Tianqing Pharmaceutical Group Co., Ltd. (CN) 2022-02-23 — — EP claimed
US-20220040317-A1 DEGRADATION OF FAK OR FAK AND ALK BY CONJUGATION OF FAK AND ALK INHIBITORS WITH E3 LIGASE LIGANDS AND METHODS OF USE DANA-FARBER CANCER INSTITUTE, INC. (US) 2022-02-10 — — US claimed
US-20220031698-A1 THERAPEUTIC COMPOSITIONS, COMBINATIONS, AND METHODS OF USE THE INSTITUTE OF CANCER RESEARCH: ROYAL CANCER HOSPITAL (GB) 2022-02-03 — — US claimed
EP-2146779-B1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH PFIZER PROD INC (US) 2016-08-10 — — EP claimed
US-20150080368-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH VERASTEM, INC. (US) 2015-03-19 — — US claimed
US-8247411-B2 Sulfonyl amide derivatives for the treatment of abnormal cell growth PFIZER INC (US) 2012-08-21 — — US claimed
US-20110166120-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH PFIZER INC. 2011-07-07 — — US claimed
EP-2146779-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH Pfizer Products Inc. (US) 2010-01-27 — — EP claimed
US-20090054395-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH PFIZER INC. 2009-02-26 — — US claimed
WO-2008129380-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH PFIZER PRODUCTS INC. (US) 2008-10-30 — — 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 (9 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-20150080368-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH GPR119, INSR, LYAR PTK2 4052/4885PTK2B 3523/4885AURKA 1617/4885
US-20110166120-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH GPR119, INSR, LYAR PTK2 4052/4885PTK2B 3523/4885AURKA 1617/4885
US-12594421-B2 Compositions and methods for increasing cancer cell sensitivity to alternating electric fields PTK2, GSK3B, MTOR PTK2 1/4885PTK2B 42/4885AURKA 173/4885
US-20260060936-A1 INDOLIUM-BASED STABILIZERS OF HYDROPHOBIC DRUGS CHRM1, CHRNA6, OPRM1 PTK2 3024/4885PTK2B 3109/4885AURKA 1893/4885
US-20220040317-A1 DEGRADATION OF FAK OR FAK AND ALK BY CONJUGATION OF FAK AND ALK INHIBITORS WITH E3 LIGASE LIGANDS AND METHODS OF USE ALK, PTK2, CBL PTK2 2/4885PTK2B 30/4885AURKA 780/4885
US-20260137839-A1 CONTROLLED HYDROGEL DELIVERY OF FOCAL ADHESION KINASE INHIBITOR FOR DECREASED SCAR FORMATION PTK2, DSTYK, CTTN PTK2 1/4885PTK2B 5/4885AURKA 806/4885
US-20260034128-A1 THERAPEUTIC COMPOSITIONS, COMBINATIONS, AND METHODS OF USE PTK2, CTTN, MAP2K2 PTK2 1/4885PTK2B 9/4885AURKA 1134/4885
US-20090054395-A1 SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH GPR119, INSR, LYAR PTK2 4052/4885PTK2B 3523/4885AURKA 1617/4885
US-20220031698-A1 THERAPEUTIC COMPOSITIONS, COMBINATIONS, AND METHODS OF USE BRAF, PTK2, NRAS PTK2 2/4885PTK2B 120/4885AURKA 362/4885

“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.

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