SCHEMBL4699731

SCHEMBL4699731

Cc1ccc(C(=O)Nc2cccc(C(F)(F)F)c2)cc1Nc1nc(-c2cccnc2)nc2c1cnn2C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ABL1 P00519 7/20 1.00
MAPK14 Q16539 5/20 1.00
DDR1 Q08345 4/20 1.00
DDR2 Q16832 4/20 1.00
LCK P06239 4/20 1.00
BRAF P15056 4/20 1.00
BCR P11274 4/20 1.00
SRC P12931 3/20 1.00
EPHB2 P29323 3/20 1.00
KDR P35968 3/20 1.00
ESYT2 A0FGR8 2/20 1.00
NBAS A2RRP1 2/20 1.00
CNOT1 A5YKK6 2/20 1.00
TBKBP1 A7MCY6 2/20 1.00
AGPS O00116 2/20 1.00
MYO1F O00160 2/20 1.00
SNAP23 O00161 2/20 1.00
AP3B1 O00203 2/20 1.00
PSMD12 O00232 2/20 1.00
BMPR1B O00238 2/20 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
SCHEMBL29380618 1.00 ABL1 (1.00) ABL1MAPK14DDR1DDR2LCK
SCHEMBL29358745 1.00 ABL1 (1.00) ABL1MAPK14DDR1DDR2LCK
SCHEMBL4697866 0.94 BRAF (0.89) ABL1MAPK14DDR1DDR2LCK
SCHEMBL4697696 0.92 BRAF (0.86) ABL1MAPK14DDR1DDR2LCK
SCHEMBL29688472 0.92 BRAF (0.86) ABL1MAPK14DDR1DDR2LCK
SCHEMBL24532059 0.92 ABL1 (0.86) ABL1MAPK14DDR1DDR2LCK
SCHEMBL23092285 0.92 BRAF (0.86) ABL1MAPK14DDR1DDR2LCK
SCHEMBL22024695 0.92 BRAF (0.86) ABL1MAPK14DDR1DDR2LCK
SCHEMBL16136600 0.91 ABL1 (0.84) ABL1MAPK14DDR1DDR2LCK
SCHEMBL24532058 0.91 ABL1 (0.83) ABL1MAPK14DDR1DDR2LCK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4378957-A2 COMBINATION THERAPIES COMPRISING ANTIBODY MOLECULES TO PD-1 Novartis AG (CH) 2024-06-05 EP claimed
US-20210251944-A1 METHODS FOR TREATING A CANCER RESISTANT TO AT LEAST ONE TYROSINE KINASE INHIBITOR DEL MAR PHARMACEUTICALS (BC) LTD. (CA) 2021-08-19 US claimed
CN-112755193-A Method of treating malignancies with anti-tyrosine kinase inhibitors using dianhydrogalactitol or a derivative thereof 德玛医药 2021-05-07 CN claimed
EP-2872161-B1 DIANHYDROGALACTITOL FOR USE IN TREATING TYROSINE-KINASE-INHIBITOR-RESISTANT MALIGNANCIES IN PATIENTS WITH GENETIC POLYMORPHISMS OR AHI1 DYSREGULATIONS OR MUTATIONS DEL MAR PHARMACEUTICALS (CA) 2020-12-16 EP claimed
US-10351916-B2 Method for identification of anti-HIV human miRNA mimics and miRNA inhibitors and anti-HIV pharmaceutical compounds CSIR (ZA) 2019-07-16 US claimed
EP-2872161-A2 METHODS FOR TREATING TYROSINE-KINASE-INHIBITOR-RESISTANT MALIGNANCIES IN PATIENTS WITH GENETIC POLYMORPHISMS OR AHI1 DYSREGULATIONS OR MUTATIONS EMPLOYING DIANHYDROGALACTITOL, DIACETYLDIANHYDROGALACTITOL, DIBROMODULCITOL, OR ANALOGS OR DERIVATIVES THEREOF Del Mar Pharmaceuticals (CA) 2015-05-20 EP claimed
WO-2014004376-A2 METHODS FOR TREATING TYROSINE-KINASE-INHIBITOR-RESISTANT MALIGNANCIES IN PATIENTS WITH GENETIC POLYMORPHISMS OR AHI1 DYSREGULATIONS OR MUTATIONS EMPLOYING DIANHYDROGALACTITOL, DIACETYLDIANHYDROGALACTITOL, DIBROMODULCITOL, OR ANALOGS OR DERIVATIVES THEREOF DEL MAR PHARMACEUTICALS (CA) 2014-01-03 WO claimed
US-20080275054-A1 3-(Substituted Amino)-Pyrazolo[3, 4-D]Pyrimidines as Ephb and Vegfr2 Kinase Inhibitors HOLZER PHILIPP 2008-11-06 US claimed
EP-1963327-A1 3-(SUBSTITUTED AMINO)-PYRAZOLO[3,4-d]PYRIMIDINES AS EPHB AND VEGFR2 KINASE INHIBITORS Novartis AG (CH) 2008-09-03 EP claimed
WO-2007062805-A1 3-(SUBSTITUTED AMINO)-PYRAZOLO[3,4-d]PYRIMIDINES AS EPHB AND VEGFR2 KINASE INHIBITORS NOVARTIS AG (CH) 2007-06-07 WO claimed
US-20260139061-A1 TREATMENT OF CANCER USING HUMANIZED ANTI-EGFRvIII CHIMERIC ANTIGEN RECEPTOR NOVARTIS AG (CH) 2026-05-21 US disclosed
US-12630633-B2 Antibody molecules to PD-1 and uses thereof NOVARTIS AG (CH) 2026-05-19 US disclosed
US-12605450-B2 C3-carbon linked glutarimide Degronimers for target protein degradation C4 THERAPEUTICS, INC. (US) 2026-04-21 US disclosed
US-12600777-B2 Combination therapies comprising antibody molecules to LAG-3 NOVARTIS AG (CH) 2026-04-14 US disclosed
EP-4717317-A2 N/O-LINKED DEGRONS AND DEGRONIMERS FOR PROTEIN DEGRADATION C4 Therapeutics, Inc. (US) 2026-04-01 EP disclosed
EP-2872161-A2 METHODS FOR TREATING TYROSINE-KINASE-INHIBITOR-RESISTANT MALIGNANCIES IN PATIENTS WITH GENETIC POLYMORPHISMS OR AHI1 DYSREGULATIONS OR MUTATIONS EMPLOYING DIANHYDROGALACTITOL, DIACETYLDIANHYDROGALACTITOL, DIBROMODULCITOL, OR ANALOGS OR DERIVATIVES THEREOF Del Mar Pharmaceuticals (CA) 2015-05-20 EP disclosed
US-20140322275-A1 TREATMENT OF CANCER USING HUMANIZED ANTI-EGFRvIII CHIMERIC ANTIGEN RECEPTOR UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION 2014-10-30 US disclosed
WO-2014031856-A1 COMBINATION THERAPY USING PI3 KINASE AND BRAF INHIBITORS ONCONTHYREON INC. (US) 2014-02-27 WO disclosed
WO-2014004376-A2 METHODS FOR TREATING TYROSINE-KINASE-INHIBITOR-RESISTANT MALIGNANCIES IN PATIENTS WITH GENETIC POLYMORPHISMS OR AHI1 DYSREGULATIONS OR MUTATIONS EMPLOYING DIANHYDROGALACTITOL, DIACETYLDIANHYDROGALACTITOL, DIBROMODULCITOL, OR ANALOGS OR DERIVATIVES THEREOF DEL MAR PHARMACEUTICALS (CA) 2014-01-03 WO disclosed
US-20080275054-A1 3-(Substituted Amino)-Pyrazolo[3, 4-D]Pyrimidines as Ephb and Vegfr2 Kinase Inhibitors HOLZER PHILIPP 2008-11-06 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 (6 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-12605450-B2 C3-carbon linked glutarimide Degronimers for target protein degradation NEDD4, UBE3A, UBE3C ABL1 2331/4885MAPK14 3625/4885DDR1 1277/4885
US-20210251944-A1 METHODS FOR TREATING A CANCER RESISTANT TO AT LEAST ONE TYROSINE KINASE INHIBITOR DCLRE1B, AIPL1, WHR1 ABL1 746/4885MAPK14 1175/4885DDR1 143/4885
US-20260139061-A1 TREATMENT OF CANCER USING HUMANIZED ANTI-EGFRvIII CHIMERIC ANTIGEN RECEPTOR EGFR, ERBB2, HAVCR2 ABL1 185/4885MAPK14 2429/4885DDR1 138/4885
US-12600777-B2 Combination therapies comprising antibody molecules to LAG-3 IGSF11, IGLV6-57, CD2 ABL1 690/4885MAPK14 3564/4885DDR1 899/4885
US-20080275054-A1 3-(Substituted Amino)-Pyrazolo[3, 4-D]Pyrimidines as Ephb and Vegfr2 Kinase Inhibitors EPHB3, EPHB2, EPHB1 ABL1 30/4885MAPK14 252/4885DDR1 483/4885
US-12630633-B2 Antibody molecules to PD-1 and uses thereof CD40, CD274, ICOS ABL1 163/4885MAPK14 829/4885DDR1 114/4885

“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.