Falnidamol

Falnidamol

SCHEMBL158563

CN1CCC(Nc2ncc3ncnc(Nc4ccc(F)c(Cl)c4)c3n2)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

EGFR

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

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
EGFR known ✓ P00533 12/20 1.00
ERBB2 P04626 5/20 1.00
HPGD P15428 1/20 1.00
HTT P42858 1/20 1.00
BCL6 P41182 2/20 0.61
MAPT P10636 1/20 0.57
CSNK2A1 P68400 1/20 0.51
BRAF P15056 2/20 0.49
AXL P30530 1/20 0.47
ERBB4 Q15303 2/20 0.47
GRM1 Q13255 1/20 0.47
JAK3 P52333 1/20 0.46

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
Falnidamol SCHEMBL29387986 1.00 EGFR (1.00) EGFRERBB2HPGDHTTBCL6
Falnidamol SCHEMBL29409569 0.99 EGFR (0.98) EGFRERBB2HPGDHTTBCL6
Falnidamol SCHEMBL29403789 0.99 EGFR (0.98) EGFRERBB2HPGDHTTBCL6
SCHEMBL8487409 0.95 EGFR (0.90) EGFRERBB2HPGDHTTBCL6
SCHEMBL8315459 0.95 EGFR (0.90) EGFRERBB2HPGDHTTBCL6
SCHEMBL8314093 0.92 EGFR (0.84) EGFRERBB2HPGDHTTBCL6
SCHEMBL6989864 0.91 EGFR (0.84) EGFRERBB2HPGDHTTBCL6
SCHEMBL8314263 0.91 EGFR (0.84) EGFRERBB2HPGDHTTBCL6
SCHEMBL8485712 0.91 EGFR (0.82) EGFRERBB2HPGDHTTBCL6
SCHEMBL6992445 0.89 EGFR (0.81) EGFRERBB2HPGDHTTBCL6

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 1241 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026107237-A1 RAS AND EGFR INHIBITORS COMBINATION THERAPY ERASCA, INC. (US) 2026-05-21 WO claimed
EP-4615506-A1 USE OF GSK-3 ACTIVATIOR TO MODULATE PROTEASOME ACTIVITY TO PREVENT AGEING ASSOCIATED CONDITIONS AND DISEASES Sahin, Fikret (TR) 2025-09-17 EP claimed
EP-4577832-A1 METHOD FOR PREDICTING THE RESPONSE TO AN INHIBITOR OF EGFR KINASE ACTIVITY Indivumed GmbH (DE) 2025-07-02 EP claimed
EP-4525870-A1 METHODS OF TREATING CUSHING'S SYNDROME AND LIVER DISORDERS, AND OF REDUCING LIVER TOXICITY OF OTHER DRUGS ADMINISTERED TO A PATIENT Corcept Therapeutics Incorporated (US) 2025-03-26 EP claimed
WO-2024258363-A1 USE OF GSK-3 ACTIVATIOR TO MODULATE PROTEASOME ACTIVITY TO PREVENT AGEING ASSOCIATED CONDITIONS AND DISEASES SAHIN FIKRET (TR) 2024-12-19 WO claimed
US-20240325363-A1 COMPOSITION FOR TREATMENT OF ANTICANCER AGENT-RESISTANT CANCER ONCOCROSS CO.,LTD. (KR) 2024-10-03 US claimed
US-20240245659-A1 Methods of Treating Cushing's Syndrome and Liver Disorders, and of Reducing Liver Toxicity of Other Drugs Administered to a Patient CORCEPT THERAPEUTICS INCORPORATED (US) 2024-07-25 US claimed
CN-118141921-A Use of CAMK2 inhibitors for the preparation of a medicament for reducing resistance to EGFR-driven cancers 四川大学 2024-06-07 CN claimed
CN-118078833-A Falnidamol application in reversing tumor multidrug resistance 山东第二医科大学 2024-05-28 CN claimed
WO-2024011307-A1 PYRAZOLO[3,4-D]PYRIMIDIN-6-YL-SULFONAMIDE DERIVATIVES FOR THE INHIBITION OF SGK-1 AND TREATMENT OF CANCER THRYV THERAPEUTICS INC. (CA) 2024-01-18 WO claimed
US-20120076781-A1 METHODS OF TREATING CANCERS WITH HER3 ANTISENSE OLIGONUCLEOTIDES SANTARIS PHARMA A/S (DK) 2012-03-29 US claimed
EP-2419110-A1 METHODS OF TREATING CANCERS WITH HER3 ANTISENSE OLIGONUCLEOTIDES Enzon Pharmaceuticals, Inc. (US) 2012-02-22 EP claimed
US-20120004285-A1 ERBB-3 (HER3)-SELECTIVE COMBINATION THERAPY ENZON PHARMACEUTICALS, INC. (US) 2012-01-05 US claimed
EP-2376087-A1 ERBB-3 (HER3)-SELECTIVE COMBINATION THERAPY Santaris Pharma A/S (DK) 2011-10-19 EP claimed
WO-2010120861-A1 METHODS OF TREATING CANCERS WITH HER3 ANTISENSE OLIGONUCLEOTIDES ENZON PHARMACEUTICALS, INC. (US) 2010-10-21 WO claimed
WO-2010054051-A1 ERBB-3 (HER3)-SELECTIVE COMBINATION THERAPY SANTARIS PHARMA A/S (DK) 2010-05-14 WO claimed
EP-0888351-B1 PYRIMIDO 5,4-D]PYRIMIDINES, MEDICAMENTS CONTAINING THESE COMPOUNDS, THEIR USE AND PROCESS FOR THEIR PRODUCTION THOMAE GMBH DR K (DE) 2003-10-15 EP claimed
EP-0779888-B1 PYRIMIDO [5,4-D]PYRIMIDINES, DRUGS CONTAINING THESE COMPOUNDS, THEIR USE, AND PROCESS FOR PREPARING THEM BOEHRINGER INGELHEIM PHARMA (DE) 1999-04-28 EP claimed
EP-0888351-A1 PYRIMIDO 5,4-D]PYRIMIDINES, MEDICAMENTS CONTAINING THESE COMPOUNDS, THEIR USE AND PROCESS FOR THEIR PRODUCTION Dr. Karl Thomae GmbH (DE) 1999-01-07 EP claimed
WO-1997032880-A1 PYRIMIDO[5,4-D]PYRIMIDINES, MEDICAMENTS CONTAINING THESE COMPOUNDS, THEIR USE AND PROCESS FOR THEIR PRODUCTION DR. KARL THOMAE GMBH (DE) 1997-09-12 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 (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-20240325363-A1 COMPOSITION FOR TREATMENT OF ANTICANCER AGENT-RESISTANT CANCER KRAS, EGFR, NRAS EGFR 2/4885ERBB2 5/4885HPGD 4224/4885
US-20240245659-A1 Methods of Treating Cushing's Syndrome and Liver Disorders, and of Reducing Liver Toxicity of Other Drugs Administered to a Patient CYP3A43, NR3C2, CYP3A5 EGFR 3381/4885ERBB2 4257/4885HPGD 600/4885
US-20120076781-A1 METHODS OF TREATING CANCERS WITH HER3 ANTISENSE OLIGONUCLEOTIDES ERBB3, ERBB2, EGFR EGFR 3/4885ERBB2 2/4885HPGD 4814/4885
US-20120004285-A1 ERBB-3 (HER3)-SELECTIVE COMBINATION THERAPY ERBB3, ERBB2, EGFR EGFR 3/4885ERBB2 2/4885HPGD 4628/4885

“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.