SCHEMBL29354959

SCHEMBL29354959

C#Cc1cccc(Nc2ncnc3cc(OCCOC)c(OCCO)cc23)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EGFR P00533 15/20 1.00
ERBB2 P04626 7/20 0.90
GAK O14976 4/20 0.90
KDR P35968 3/20 0.90
ILK Q13418 2/20 0.90
FLT1 P17948 2/20 0.90
RIPK2 O43353 2/20 0.90
BUB1 O43683 2/20 0.90
STK10 O94804 2/20 0.90
ABL1 P00519 2/20 0.90
LCK P06239 2/20 0.90
LYN P07948 2/20 0.90
RET P07949 2/20 0.90
SRC P12931 2/20 0.90
FGFR2 P21802 2/20 0.90
FECH P22830 2/20 0.90
FLT3 P36888 2/20 0.90
MAP3K1 Q13233 2/20 0.90
PLK4 O00444 1/20 0.90
CIT O14578 1/20 0.90

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
SCHEMBL1507409 1.00 EGFR (1.00) EGFRERBB2GAKKDRILK
SCHEMBL1507627 1.00 EGFR (1.00) EGFRERBB2GAKKDRILK
SCHEMBL2435950 1.00 EGFR (1.00) EGFRERBB2GAKKDRILK
Hydrochloric Acid SCHEMBL1507689 0.99 EGFR (0.98) EGFRERBB2GAKKDRILK
Hydrochloric Acid SCHEMBL1507491 0.99 EGFR (0.98) EGFRERBB2GAKKDRILK
Erlotinib SCHEMBL29120903 0.95 EGFR (0.96) EGFRERBB2GAKKDRILK
Erlotinib SCHEMBL3667407 0.95 EGFR (1.00) EGFRERBB2GAKKDRILK
Erlotinib SCHEMBL8413 0.95 EGFR (1.00) EGFRERBB2GAKKDRILK
Erlotinib SCHEMBL29351329 0.95 EGFR (1.00) EGFRERBB2GAKKDRILK
Erlotinib SCHEMBL30362833 0.95 EGFR (1.00) EGFRERBB2GAKKDRILK

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 667 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-4615869-A1 COMBINATION THERAPY COMPRISING BISPECIFIC ANTIBODIES COMPRISING AN NRP1 BINDING DOMAIN Pinetree Therapeutics, Inc. (US) 2025-09-17 EP claimed
WO-2024102187-A1 COMBINATION THERAPY COMPRISING BISPECIFIC ANTIBODIES COMPRISING AN NRP1 BINDING DOMAIN PINETREE THERAPEUTICS, INC. (US) 2024-05-16 WO 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-11723891-B2 Drug combinations for use in the treatment of RAS-mutant cancer UMC UTRECHT HOLDING B.V. (NL) 2023-08-15 US claimed
US-11692028-B2 Map kinase pathway targets for the treatment of Marfan syndrome THE JOHNS HOPKINS UNIVERSITY (US) 2023-07-04 US claimed
US-20230130791-A1 A Combined Inhibition of EGFR and NRF2 in The Treatment of Malignant Glioma THE UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS 2023-04-27 US claimed
US-20230119324-A1 EGFR INHIBITION TRIGGERS AN ADAPTIVE RESPONSE BY CO-OPTING ANTIVIRAL SIGNALING PATHWAYS IN LUNG CANCER THE UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS 2023-04-20 US claimed
US-11612601-B1 Targeting epidermal growth factor to treat vascular calcification THE FLORIDA INTERNATIONAL UNIVERSITY BOARD OF TRUSTEES (US) 2023-03-28 US claimed
EP-4117788-A1 COMBINED INHIBITION OF EGFR AND NRF2 IN THE TREATMENT OF MALIGNANT GLIOMA UNITED STATES GOVERNMENT as represented by THE DEPARTMENT OF VETERANS AFFAIRS (US) 2023-01-18 EP claimed
EP-4106879-A1 IDENTIFICATION OF AN EGFR-BIN3 PATHWAY THAT ACTIVELY SUPPRESSES INVASION AND REDUCES TUMOR SIZE IN GLIOBLASTOMA United States Government as Represented by The Department of Veterans Affairs (US) 2022-12-28 EP claimed
EP-4106793-A1 EGFR INHIBITION TRIGGERS AN ADAPTIVE RESPONSE BY CO-OPTING ANTIVIRAL SIGNALING PATHWAYS IN LUNG CANCER United States Government as Represented by The Department of Veterans Affairs (US) 2022-12-28 EP claimed
US-11389434-B2 Methods and pharmaceutical compositions for the treatment of mast cell diseases INSERM (FR) 2022-07-19 US claimed
US-20220218682-A1 COMPOSITIONS AND METHODS FOR TREATING CANCER THE UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS 2022-07-14 US claimed
US-20220211706-A1 Methods and Compositions for Treating Cancer UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS 2022-07-07 US claimed
US-11285154-B2 Methods and compositions for treating cancer UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS (US) 2022-03-29 US claimed
US-20220079935-A1 COMPOUNDS AND TREATMENTS THAT ENHANCE ENTERIC NERVOUS SYSTEM FUNCTION UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION 2022-03-17 US claimed
EP-3965896-A1 COMPOSITIONS AND METHODS FOR TREATING CANCER The United States Government as Represented by the Department of Veterans Affairs (US) 2022-03-16 EP claimed
EP-3704090-B1 MODULATORS OF THE INTEGRATED STRESS PATHWAY CALICO LIFE SCIENCES LLC (US) 2026-05-27 EP disclosed
CN-215643385-U Device for direct drug infusion 基因泰克股份有限公司 2022-01-25 CN 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 (2 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-20220079935-A1 COMPOUNDS AND TREATMENTS THAT ENHANCE ENTERIC NERVOUS SYSTEM FUNCTION NTRK2, BDNF, NTSR2 EGFR 1010/4885ERBB2 630/4885GAK 1831/4885
US-11389434-B2 Methods and pharmaceutical compositions for the treatment of mast cell diseases KIT, SHH, CMA1 EGFR 464/4885ERBB2 560/4885GAK 1074/4885

“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.