Procodazole

Procodazole

SCHEMBL838841

O=C(O)CCc1nc2ccccc2[nH]1.O=C(O)CCc1nc2ccccc2[nH]1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
CHRM1 P11229 1/20 1.00
KDM4E B2RXH2 2/20 0.68
PARP1 P09874 1/20 0.68
PARP2 Q9UGN5 1/20 0.68
CYP1A2 P05177 1/20 0.67
CYP2C9 P11712 1/20 0.67
MAPT P10636 1/20 0.65
APEX1 P27695 1/20 0.64
POLB P06746 1/20 0.64
NPC1 O15118 1/20 0.63
RAB9A P51151 1/20 0.63
PDE10A Q9Y233 1/20 0.60
GAA P10253 1/20 0.60
HTT P42858 1/20 0.60
PRKAG1 P54619 2/20 0.59
PRKAA2 P54646 2/20 0.59
PRKAB1 Q9Y478 2/20 0.59
ALDH1A1 P00352 1/20 0.59
PRKAA1 Q13131 1/20 0.59

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
Procodazole SCHEMBL29404024 1.00 CHRM1 (1.00) CHRM1KDM4EPARP1PARP2CYP1A2
Procodazole SCHEMBL349966 1.00 CHRM1 (1.00) CHRM1KDM4EPARP1PARP2CYP1A2
Procodazole SCHEMBL5413283 0.95 CHRM1 (0.91) CHRM1KDM4EPARP1PARP2CYP1A2
SCHEMBL2017763 0.90 CHRM1 (0.82) CHRM1KDM4ECYP1A2CYP2C9MAPT
SCHEMBL7433457 0.89 CHRM1 (0.80) CHRM1KDM4ECYP1A2CYP2C9MAPT
SCHEMBL14565997 0.88 CHRM1 (0.78) CHRM1KDM4ECYP1A2CYP2C9MAPT
SCHEMBL12999426 0.86 GAA (0.75) CHRM1KDM4ECYP1A2CYP2C9MAPT
SCHEMBL4573158 0.85 CHRM1 (0.74) CHRM1KDM4ECYP1A2CYP2C9MAPT
SCHEMBL19368796 0.85 CHRM1 (0.74) CHRM1KDM4ECYP1A2CYP2C9MAPT
SCHEMBL5717769 0.85 CHRM1 (0.74) CHRM1KDM4ECYP1A2CYP2C9MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3703653-A1 COMPOSITIONS AND METHODS FOR CANCER TREATMENT University Of Virginia Patent Foundation (US) 2020-09-09 EP disclosed
US-20200268665-A1 COMPOSITIONS AND METHODS FOR CANCER TREATMENT UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2020-08-27 US disclosed
US-8968702-B2 Inhibition of HIF-1 activation for anti-tumor and anti-inflammatory responses DUKE UNIVERSITY (US) 2015-03-03 US disclosed
US-8865130-B2 Methods and compositions for diagnostic and therapeutic targeting of COX-2 VANDERBILT UNIVERSITY (US) 2014-10-21 US disclosed
US-20140249097-A1 Inhibition of HIF-1 activation for Anti-Tumor and Anti-Inflammatory responses DUKE UNIVERSITY 2014-09-04 US disclosed
US-20130052138-A1 METHODS AND COMPOSITIONS FOR DIAGNOSTIC AND THERAPEUTIC TARGETING OF COX-2 VANDERBILT UNIVERSITY (US) 2013-02-28 US disclosed
US-8143302-B2 Methods and compositions for diagnostic and therapeutic targeting of COX-2 VANDERBILT UNIVERSITY (US) 2012-03-27 US disclosed
US-20110054023-A1 Inhibition of HIF-1 activation for anti-tumor and anti-inflammatory responses DUKE UNIVERSITY (US) 2011-03-03 US disclosed
US-20100254910-A1 METHODS AND COMPOSITIONS FOR DIAGNOSTIC AND THERAPEUTIC TARGETING OF COX-2 VANDERBILT UNIVERSITY (US) 2010-10-07 US disclosed
US-7736624-B2 derivatives of non-steroidal anti-inflammatory drugs that exhibit selective binding to cyclooxygenase-2 (COX-2) and that comprise functional groups allowing them to be used for medical diagnosis and/or as therapeutic agents; tissue-targeted therapy UNIV VANDERBILT (US) 2010-06-15 US disclosed
EP-2040699-A2 METHODS AND COMPOSITIONS FOR DIAGNOSTIC AND THERAPEUTIC TARGETING OF COX-2 Vanderbilt University Medical Center (US) 2009-04-01 EP disclosed
US-20070297984-A1 Inhibition of HIF-1 activation for anti-tumor and anti-inflammatory responses DUKE UNIVERSITY (US) 2007-12-27 US disclosed
WO-2007149456-A2 METHODS AND COMPOSITIONS FOR DIAGNOSTIC AND THERAPEUTIC TARGETING OF COX-2 VANDERBILT UNIVERSITY (US) 2007-12-27 WO disclosed
US-20070292352-A1 derivatives of non-steroidal anti-inflammatory drugs that exhibit selective binding to cyclooxygenase-2 (COX-2) and that comprise functional groups allowing them to be used for medical diagnosis and/or as therapeutic agents; tissue-targeted therapy VANDERBILT UNIVERSITY (US) 2007-12-20 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 (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-20100254910-A1 METHODS AND COMPOSITIONS FOR DIAGNOSTIC AND THERAPEUTIC TARGETING OF COX-2 PTGS2, PTGES2, PTGER2 CHRM1 4174/4885KDM4E 4585/4885PARP1 2959/4885
US-20070292352-A1 derivatives of non-steroidal anti-inflammatory drugs that exhibit selective binding to cyclooxygenase-2 (COX-2) and that comprise functional groups allowing them to be used for medical diagnosis and/or as therapeutic agents; tissue-targeted therapy PTGES2, PTGS2, PTGER2 CHRM1 3673/4885KDM4E 4440/4885PARP1 3625/4885
US-20130052138-A1 METHODS AND COMPOSITIONS FOR DIAGNOSTIC AND THERAPEUTIC TARGETING OF COX-2 PTGS2, PTGES2, PTGER2 CHRM1 4174/4885KDM4E 4585/4885PARP1 2959/4885

“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.