SCHEMBL505584

SCHEMBL505584

O=c1c(O)c(-c2ccc(O)c(O)c2)oc2ccc(O)cc12

nearest known ligand 0.79

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 13/20 0.79
KMT2A Q03164 13/20 0.79
CYP3A4 P08684 11/20 0.79
HSD17B10 Q99714 11/20 0.79
KDM4E B2RXH2 10/20 0.79
MAPT P10636 9/20 0.79
CYP2C9 P11712 7/20 0.79
ALOX15 P16050 7/20 0.79
TP53 P04637 6/20 0.79
RECQL P46063 6/20 0.79
MAPK1 P28482 6/20 0.79
ALDH1A1 P00352 6/20 0.79
HPGD P15428 6/20 0.79
CDK2 P24941 4/20 0.79
LMNA P02545 4/20 0.79
CASP1 P29466 4/20 0.79
CASP7 P55210 4/20 0.79
CDK5 Q00535 3/20 0.79
CDK5R1 Q15078 3/20 0.79
ALOX12 P18054 3/20 0.79

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
Fisetin SCHEMBL29381611 0.88 MEN1 (1.00) MEN1KMT2ACYP3A4HSD17B10KDM4E
Fisetin SCHEMBL116861 0.88 MEN1 (1.00) MEN1KMT2ACYP3A4HSD17B10KDM4E
Fisetin SCHEMBL39454 0.88 MEN1 (1.00) MEN1KMT2ACYP3A4HSD17B10KDM4E
Fisetin SCHEMBL29394036 0.88 MEN1 (1.00) MEN1KMT2ACYP3A4HSD17B10KDM4E
Fisetin SCHEMBL29349742 0.88 MEN1 (1.00) MEN1KMT2ACYP3A4HSD17B10KDM4E
SCHEMBL2281134 0.88 MEN1 (1.00) MEN1KMT2ACYP3A4HSD17B10KDM4E
Fisetin SCHEMBL4263659 0.87 CDK5 (1.00) MEN1KMT2ACYP3A4HSD17B10KDM4E
SCHEMBL10037939 0.86 MEN1 (0.76) MEN1KMT2ACYP3A4HSD17B10KDM4E
SCHEMBL7660823 0.86 MEN1 (0.68) MEN1KMT2ACYP3A4HSD17B10KDM4E
SCHEMBL7652737 0.86 MEN1 (0.68) MEN1KMT2ACYP3A4HSD17B10KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023150072-A1 COMPOSITIONS AND METHODS FOR THE PRESERVATION OF PLANT MATTER SINCLAIR DAVID A (US) 2023-08-10 WO claimed
US-20160367497-A1 METHODS AND COMPOSITIONS FOR TREATING NEUROPATHIES WASHINGTON UNIVERSITY 2016-12-22 US claimed
EP-2670404-A1 SIRTUIN MODULATORS AS VIRUS PRODUCTION MODULATORS The Trustees of Princeton University (US) 2013-12-11 EP claimed
WO-2012106509-A1 SIRTUIN MODULATORS AS VIRUS PRODUCTION MODULATORS THE TRUSTEES OF PRINCETON UNIVERSITY (US) 2012-08-09 WO claimed
US-20100047177-A1 METHODS AND COMPOSITIONS FOR TREATING NEUROPATHIES WASHINGTON UNIVERSITY (US) 2010-02-25 US claimed
EP-2124985-A2 METHODS AND COMPOSITIONS FOR TREATING NEUROPATHIES WASHINGTON UNIVERSITY (US) 2009-12-02 EP claimed
EP-1991205-A1 OCULAR THERAPY USING SIRTUIN-ACTIVATING AGENTS Allergan, Inc. (US) 2008-11-19 EP claimed
WO-2008091710-A2 METHODS AND COMPOSITIONS FOR TREATING NEUROPATHIES WASHINGTON UNIVERSITY (US) 2008-07-31 WO claimed
WO-2007103960-A1 OCULAR THERAPY USING SIRTUIN-ACTIVATING AGENTS ALLERGAN, INC. (US) 2007-09-13 WO claimed
US-20070212395-A1 Ocular therapy using sirtuin-activating agents ALLERGAN, INC. (US) 2007-09-13 US claimed
EP-1755391-A2 METHODS AND COMPOSITIONS FOR TREATING NEUROPATHIES WASHINGTON UNIVERSITY (US) 2007-02-28 EP claimed
US-20060084135-A1 Compositions for manipulating the lifespan and stress response of cells and organisms BIOMOL INTERNATIONAL, INC. 2006-04-20 US claimed
US-20060002914-A1 treating or preventing axonal degradation in neuropathic diseases in mammals; axonopathy; administering an agent (such as NAD, NADH) that increases sirtuin activity in diseased and/or injured neurons and supporting cells in an amount effective to decrease axonal degeneration NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2006-01-05 US claimed
WO-2006001982-A2 METHODS AND COMPOSITIONS FOR TREATING NEUROPATHIES WASHINGTON UNIVERSITY (US) 2006-01-05 WO claimed
EP-1109800-A1 NOVEL CDK INHIBITORS HAVING FLAVONE STRUCTURE LG CHEMICAL LIMITED (KR) 2001-06-27 EP claimed
WO-2000012496-A1 NOVEL CDK INHIBITORS HAVING FLAVONE STRUCTURE LG CHEMICAL LTD. (KR) 2000-03-09 WO claimed
EP-4709405-A2 FLUORESCEIN-LABELED NERVE TARGETING PEPTIDE FORMULATIONS AND RELATED METHODS Alume Biosciences, Inc. (US) 2026-03-18 EP disclosed
US-12533425-B2 Methods and systems using peptides for targeting and mapping human nerves in image guided surgery, diagnostics and therapeutic delivery ALUME BIOSCIENCES, INC. (US) 2026-01-27 US disclosed
EP-1109800-A1 NOVEL CDK INHIBITORS HAVING FLAVONE STRUCTURE LG CHEMICAL LIMITED (KR) 2001-06-27 EP disclosed
WO-2000012496-A1 NOVEL CDK INHIBITORS HAVING FLAVONE STRUCTURE LG CHEMICAL LTD. (KR) 2000-03-09 WO 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-12533425-B2 Methods and systems using peptides for targeting and mapping human nerves in image guided surgery, diagnostics and therapeutic delivery NGLY1, VGF, GAP43 MEN1 1105/4885KMT2A 4260/4885CYP3A4 4828/4885
US-20070212395-A1 Ocular therapy using sirtuin-activating agents SIRT1, SIRT2, SIRT7 MEN1 3456/4885KMT2A 642/4885CYP3A4 4777/4885

“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.