SCHEMBL2329685

SCHEMBL2329685

COc1ccc(C=CC(=O)c2cc(OC)c(OC)c(OC)c2)cc1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TUBB1 Q9H4B7 9/20 1.00
TUBB4A P04350 5/20 1.00
TUBB P07437 5/20 1.00
TUBA3C P0DPH7 5/20 1.00
TUBA1B P68363 5/20 1.00
TUBA4A P68366 5/20 1.00
TUBB4B P68371 5/20 1.00
TUBB3 Q13509 5/20 1.00
TUBB2A Q13885 5/20 1.00
TUBB8 Q3ZCM7 5/20 1.00
TUBA3E Q6PEY2 5/20 1.00
TUBA1A Q71U36 5/20 1.00
TUBA1C Q9BQE3 5/20 1.00
TUBB6 Q9BUF5 5/20 1.00
TUBB2B Q9BVA1 5/20 1.00
ABCG2 Q9UNQ0 2/20 0.78
ABCB1 P08183 2/20 0.72
CALM1 P0DP23 1/20 0.70
BACE1 P56817 1/20 0.70
TNFRSF1A P19438 1/20 0.68

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
SCHEMBL30504103 1.00 TUBB1 (1.00) TUBB1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL2329679 1.00 TUBB1 (1.00) TUBB1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL13674866 0.92 TUBB1 (0.85) TUBB1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL1425136 0.90 TUBB1 (0.81) TUBB1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL1425140 0.90 TUBB1 (0.81) TUBB1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL31059019 0.89 TUBB1 (0.80) TUBB1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL31059014 0.89 TUBB1 (0.80) TUBB1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL31059031 0.89 TUBB1 (0.80) TUBB1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL30777911 0.89 TUBB1 (1.00) TUBB1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL12709765 0.89 TUBB1 (1.00) TUBB1TUBB4ATUBBTUBA3CTUBA1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-8188546-A None JP disclosed
US-9155724-B2 Combination methods for treatment of disease WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH (US) 2015-10-13 US disclosed
EP-2670739-B1 BENZOTHIAZOLE HYBRIDS USEFUL AS ANTICANCER AGENTS AND PROCESS FOR THE PREPARATION THEREOF COUNCIL SCIENT IND RES (IN) 2015-04-01 EP disclosed
CN-104292140-A Farnesyl thiosalicylic acid analogue containing chalcone framework, preparation method and purpose thereof UNIV NANTONG 2015-01-21 CN disclosed
US-8921552-B2 Benzothiazole hybrids useful as anticancer agents and process for the preparation thereof COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2014-12-30 US disclosed
US-20140039190-A1 BENZOTHIAZOLE HYBRIDS USEFUL AS ANTICANCER AGENTS AND PROCESS FOR THE PREPARATION THEREOF COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2014-02-06 US disclosed
EP-2670739-A1 BENZOTHIAZOLE HYBRIDS USEFUL AS ANTICANCER AGENTS AND PROCESS FOR THE PREPARATION THEREOF Council Of Scientific & Industrial Research (IN) 2013-12-11 EP disclosed
US-20130053415-A1 COMBINATION METHODS FOR TREATMENT OF DISEASE NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2013-02-28 US disclosed
EP-2544686-A2 COMBINATION METHODS FOR TREATMENT OF DISEASE Whitehead Institute For Biomedical Research (US) 2013-01-16 EP disclosed
WO-2012104875-A1 BENZOTHIAZOLE HYBRIDS USEFUL AS ANTICANCER AGENTS AND PROCESS FOR THE PREPARATION THEREOF COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2012-08-09 WO disclosed
EP-1069915-B1 HYDROXYLATION ACTIVATED DRUG RELEASE UNIV MONTFORT (GB) 2003-06-25 EP disclosed
WO-2003048096-A1 SUBSTITUTED ARYL-CYCLOALKANES, AND USE THEREOF AS ANTICANCER AGENTS AVENTIS PHARMA S.A. (FR) 2003-06-12 WO disclosed
US-6346550-B2 TYROSINE KINASE INHIBITOR; ANTITUMOR AGENT DE MONTFORT UNIVERSITY (GB) 2002-02-12 US disclosed
US-20010021717-A1 Hydroxylation activated prodrugs DE MONTFORT UNIVERSITY 2001-09-13 US disclosed
US-6214886-B1 INHIBITING GROWTH OF TUMOR CELLS VIA STYRENE-DERIVED PRODRUGS WHICH ARE ACTIVATED BY ACTIVITY OF A HYDROXYLASE DEMONTFORT UNIVERSITY, THE GATEWAY (GB) 2001-04-10 US disclosed
EP-1069915-A2 HYDROXYLATION ACTIVATED DRUG RELEASE DE MONTFORT UNIVERSITY (GB) 2001-01-24 EP disclosed
EP-1051383-A1 HYDROXYLATION ACTIVATED PRODRUGS DE MONTFORT UNIVERSITY (GB) 2000-11-15 EP disclosed
WO-1999040944-A2 HYDROXYLATION ACTIVATED DRUG RELEASE DE MONTFORT UNIVERSITY (GB) 1999-08-19 WO disclosed
WO-1999040056-A1 HYDROXYLATION ACTIVATED PRODRUGS DE MONTFORT UNIVERSITY (GB) 1999-08-12 WO disclosed
JP-H08188546-A CHALCONE DERIVATIVE KYOWA HAKKO KOGYO CO LTD 1996-07-23 JP 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-20140039190-A1 BENZOTHIAZOLE HYBRIDS USEFUL AS ANTICANCER AGENTS AND PROCESS FOR THE PREPARATION THEREOF TP53, MCL1, SDHA TUBB1 105/4885TUBB4A 40/4885TUBB 112/4885
US-20010021717-A1 Hydroxylation activated prodrugs CYP1B1, CYP1A1, CYP1A2 TUBB1 1985/4885TUBB4A 2099/4885TUBB 2189/4885
US-20130053415-A1 COMBINATION METHODS FOR TREATMENT OF DISEASE NFATC1, IRF3, BCOR TUBB1 439/4885TUBB4A 969/4885TUBB 585/4885

“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.