SCHEMBL3469324

SCHEMBL3469324

COc1c(O)c2c(=O)cc(OC)c3c4c(OC)cc(=O)c5c(O)c(OC)c(CC(C)OC(=O)c6ccccc6)c(c(c1CC(C)OC(=O)Oc1ccc(O)cc1)c23)c54

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CTNNB1 P35222 8/20 1.00
TCF4 P15884 7/20 1.00
MAPT P10636 3/20 1.00
CDH1 P12830 2/20 1.00
APC P25054 2/20 1.00
TCF7L2 Q9NQB0 2/20 1.00
THRB P10828 2/20 1.00
SYK P43405 1/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
MGAM O43451 2/20 0.33
GAA P10253 2/20 0.33
SI P14410 2/20 0.33
MGAM2 Q2M2H8 2/20 0.33
KDM4E B2RXH2 1/20 0.32
POLB P06746 1/20 0.32
ADORA3 P0DMS8 1/20 0.32
MEN1 O00255 1/20 0.32
RECQL P46063 1/20 0.32
KMT2A Q03164 1/20 0.32
TDP1 Q9NUW8 1/20 0.32

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
SCHEMBL29525736 1.00 CTNNB1 (1.00) CTNNB1TCF4MAPTCDH1APC
SCHEMBL29372562 1.00 CTNNB1 (1.00) CTNNB1TCF4MAPTCDH1APC
SCHEMBL29711243 0.90 CTNNB1 (0.81) CTNNB1TCF4MAPTCDH1APC
SCHEMBL29711326 0.88 CTNNB1 (0.78) CTNNB1TCF4MAPTCDH1APC
Calphostin C SCHEMBL13827621 0.88 CTNNB1 (0.79) CTNNB1TCF4MAPTCDH1APC
Calphostin C SCHEMBL15185703 0.88 CTNNB1 (0.79) CTNNB1TCF4MAPTCDH1APC
SCHEMBL29711331 0.87 CTNNB1 (0.76) CTNNB1TCF4MAPTCDH1APC
SCHEMBL16500263 0.84 CTNNB1 (0.73) CTNNB1TCF4MAPTCDH1APC
SCHEMBL13820267 0.80 CTNNB1 (0.67) CTNNB1TCF4MAPTCDH1APC
SCHEMBL22965109 0.77 CTNNB1 (0.63) CTNNB1TCF4MAPTCDH1APC

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240315965-A1 COMPOSITIONS AND METHODS RELATED TO PHARMACEUTICAL EXCIPIENTS Natural Extraction Systems, LLC (US) 2024-09-26 US claimed
WO-2022182527-A1 COMPOSITIONS AND METHODS RELATED TO PHARMACEUTICAL EXCIPIENTS Natural Extraction Systems, LLC (US) 2022-09-01 WO claimed
US-9730926-B2 Combination therapy using bispecific anti-c-Met/anti-EGFR antibody and c-Src inhibitor SAMSUNG ELECTRONICS CO., LTD. (KR) 2017-08-15 US claimed
US-20150216972-A1 COMBINATION THERAPY USING BISPECIFIC ANTI-C-MET/ANTI-EGFR ANTIBODY AND C-SRC INHIBITOR SAMSUNG ELECTRONICS CO., LTD. (KR) 2015-08-06 US claimed
EP-4567102-A1 METHODS FOR ISOLATING EMBRYONIC STEM CELLS FROM AVIAN EMBRYONIC CELLS Suprême (FR) 2025-06-11 EP disclosed
US-12036218-B2 Modulators of airway basal cells for the treatment or prevention of lung diseases Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e. V. (DE) 2024-07-16 US disclosed
US-20230338340-A1 Methods of Treating Cystic Fibrosis DARTMOUTH COLLEGE (US) 2023-10-26 US disclosed
US-20230338340-A1 Methods of Treating Cystic Fibrosis DARTMOUTH COLLEGE (US) 2023-10-26 US disclosed
US-20230338340-A1 Methods of Treating Cystic Fibrosis DARTMOUTH COLLEGE (US) 2023-10-26 US disclosed
EP-3784240-B1 WNT6 AS GLIOBLASTOMA ONCOGENIC BIOMARKER, AND USES OF INHIBITORS THEREOF FOR TREATING WNT6-OVEREXPRESSING GLIOBLASTOMA UNIV DO MINHO (PT) 2023-09-20 EP disclosed
US-20230285556-A1 METHODS AND COMPOSITIONS FOR TREATING CANCER OMEROS CORPORATION 2023-09-14 US disclosed
WO-2023039578-A1 METHODS AND COMPOSITIONS FOR TREATING CANCER OMEROS CORPORATION (US) 2023-03-16 WO disclosed
EP-3784240-A2 A NOVEL ONCOGENE BIOMARKER, METHOD AND USES THEREOF Universidade do Minho (PT) 2021-03-03 EP disclosed
US-20210041443-A1 WNT6 AS GLIOBLASTOMA ONCOGENIC BIOMARKER, AND USES OF INHIBITORS THEREOF UNIVERSIDADE DO MINHO (PT) 2021-02-11 US disclosed
US-10624949-B1 Methods for treating diseases related to the wnt pathway NATIONAL TECHNOLOGY & ENGINEERING SOLUTIONS OF SANDIA, LLC (US) 2020-04-21 US disclosed
US-9730926-B2 Combination therapy using bispecific anti-c-Met/anti-EGFR antibody and c-Src inhibitor SAMSUNG ELECTRONICS CO., LTD. (KR) 2017-08-15 US disclosed
US-20150216972-A1 COMBINATION THERAPY USING BISPECIFIC ANTI-C-MET/ANTI-EGFR ANTIBODY AND C-SRC INHIBITOR SAMSUNG ELECTRONICS CO., LTD. (KR) 2015-08-06 US disclosed
EP-2431386-B1 Na+/Mg2+ exchanger FBN LEIBNIZ INST FÜR NUTZTIERBIOLOGIE (DE) 2015-02-25 EP disclosed
WO-2010043561-A2 REGENERATIVE THERAPY MEDIZINISCHE UNIVERSITÄT WIEN (AT) 2010-04-22 WO disclosed
EP-2177218-A1 Regenerative therapy Medizinische Universität Wien (AT) 2010-04-21 EP 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 (3 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-20150216972-A1 COMBINATION THERAPY USING BISPECIFIC ANTI-C-MET/ANTI-EGFR ANTIBODY AND C-SRC INHIBITOR SRC, MET, EGFR CTNNB1 1049/4885TCF4 3100/4885MAPT 1116/4885
US-20230338340-A1 Methods of Treating Cystic Fibrosis CFTR, DAB2IP, CTTN CTNNB1 312/4885TCF4 1501/4885MAPT 4546/4885
US-20230285556-A1 METHODS AND COMPOSITIONS FOR TREATING CANCER TP53, CD4, MCL1 CTNNB1 1218/4885TCF4 1490/4885MAPT 3945/4885

“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.