SCHEMBL3483739

SCHEMBL3483739

CC(=O)Oc1cc(C=Cc2ccc(OC(=O)CCl)cc2)cc(OC(C)=O)c1

nearest known ligand 0.77

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TTR P02766 2/20 0.77
▸ MAPT P10636 2/20 0.77
▸ LMNA P02545 2/20 0.77
▸ KDM4E B2RXH2 1/20 0.77
▸ MEN1 O00255 1/20 0.77
▸ TP53 P04637 1/20 0.77
▸ CYP3A4 P08684 1/20 0.77
▸ KMT2A Q03164 1/20 0.77
▸ SMN1; SMN2 Q16637 1/20 0.77
▸ CYP19A1 P11511 2/20 0.62
▸ TUBB4A P04350 3/20 0.55
▸ TUBB P07437 3/20 0.55
▸ TUBA3C P0DPH7 3/20 0.55
▸ TUBA1B P68363 3/20 0.55
▸ TUBA4A P68366 3/20 0.55
▸ TUBB4B P68371 3/20 0.55
▸ TUBB3 Q13509 3/20 0.55
▸ TUBB2A Q13885 3/20 0.55
▸ TUBB8 Q3ZCM7 3/20 0.55
▸ TUBA3E Q6PEY2 3/20 0.55

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
SCHEMBL13259316 1.00 TTR (0.77) TTRMAPTLMNAKDM4EMEN1
SCHEMBL28462778 0.88 KMT2A (0.82) TTRMAPTLMNAKDM4EMEN1
Triacetylresveratrol SCHEMBL717979 0.88 TTR (1.00) TTRMAPTLMNAKDM4EMEN1
Triacetylresveratrol SCHEMBL717980 0.88 TTR (1.00) TTRMAPTLMNAKDM4EMEN1
SCHEMBL20786804 0.87 TTR (0.79) TTRMAPTLMNAKDM4EMEN1
SCHEMBL3683227 0.84 KMT2A (0.75) TTRMAPTLMNAKDM4EMEN1
SCHEMBL3687875 0.84 KMT2A (0.75) TTRMAPTLMNAKDM4EMEN1
SCHEMBL28467186 0.83 KMT2A (0.73) TTRMAPTLMNAKDM4EMEN1
SCHEMBL28462780 0.83 KMT2A (0.73) TTRMAPTLMNAKDM4EMEN1
SCHEMBL28467188 0.83 KMT2A (0.73) TTRMAPTLMNAKDM4EMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1753708-B1 NOVEL SIRTUIN ACTIVATING COMPOUNDS AND METHODS FOR MAKING THE SAME UNIV BRIGHAM YOUNG (US) 2018-02-21 — — EP disclosed
US-9585907-B2 Methods and compositions for modulating Tau levels THE J. DAVID GLADSTONE INSTITUTES (US) 2017-03-07 — — US disclosed
US-20160015733-A1 METHODS AND COMPOSITIONS FOR MODULATING TAU LEVELS THE J. DAVID GLADSTONE INSTITUTES 2016-01-21 — — US disclosed
US-9040521-B2 Methods and compositions for modulating tau levels THE J. DAVID GLADSTONE INSTITUTES (US) 2015-05-26 — — US disclosed
US-8841477-B2 Sirtuin activating compounds and processes for making the same BRIGHAM YOUNG UNIVERSITY (US) 2014-09-23 — — US disclosed
US-8748464-B2 Use of SIRT1 activators or inhibitors to modulate an immune response THE J. DAVID GLADSTONE INSTITUTES (US) 2014-06-10 — — US disclosed
US-20140030295-A1 Use of Sirt1 Activators or Inhibitors to Modulate an Immune Response THE J. DAVID GLADSTONE INSTITUTES (US) 2014-01-30 — — US disclosed
US-20120225864-A1 Methods and Compositions for Modulating Tau Levels THE J. DAVID GLADSTONE INSTITUTES 2012-09-06 — — US disclosed
US-20100330114-A1 Use of SIRT1 Activators or Inhibitors to Modulate an Immune Response NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2010-12-30 — — US disclosed
US-20100185006-A1 NOVEL SIRTUIN ACTIVATING COMPOUNDS AND PROCESSES FOR MAKING THE SAME BRIGHAM YOUNG UNIVERSITY (US) 2010-07-22 — — US disclosed
US-7714161-B2 N-heterocyclic carbon-type ligand coupling in the presence of a base with benzyol halide and styrene coupling partners; resveratrol; increased stability for use in the food, cosmetic and pharmaceutical industries BRIGHAM YOUNG UNIVERSITY (US) 2010-05-11 — — US disclosed
WO-2009099643-A1 USE OF SIRT1 ACTIVATORS OR INHIBITORS TO MODULATE AN IMMUNE RESPONSE THE J. DAVID GLADSTONE INSTITUTES (US) 2009-08-13 — — WO disclosed
US-20080255382-A1 N-heterocyclic carbon-type ligand coupling in the presence of a base with benzyol halide and styrene coupling partners; resveratrol; increased stability for use in the food, cosmetic and pharmaceutical industries BRIGHAM YOUNG UNIVERSITY 2008-10-16 — — US disclosed
EP-1753708-A4 NOVEL SIRTUIN ACTIVATING COMPOUNDS AND METHODS FOR MAKING THE SAME UNIV BRIGHAM YOUNG (US) 2007-12-26 — — EP disclosed
EP-1753708-A2 NOVEL SIRTUIN ACTIVATING COMPOUNDS AND METHODS FOR MAKING THE SAME Brigham Young University (US) 2007-02-21 — — EP disclosed
WO-2005069998-A2 NOVEL SIRTUIN ACTIVATING COMPOUNDS AND METHODS FOR MAKING THE SAME BRIGHAM YOUNG UNIVERSITY TECHNOLOGY TRANSFER OFFICE (US) 2005-08-04 — — 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 (6 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-20100330114-A1 Use of SIRT1 Activators or Inhibitors to Modulate an Immune Response SIRT1, SIRT2, NFATC1 TTR 4829/4885MAPT 2086/4885LMNA 4750/4885
US-20120225864-A1 Methods and Compositions for Modulating Tau Levels MAPT, NEFM, PSEN2 TTR 38/4885MAPT 1/4885LMNA 761/4885
US-20140030295-A1 Use of Sirt1 Activators or Inhibitors to Modulate an Immune Response SIRT1, SIRT2, NFATC1 TTR 4829/4885MAPT 2086/4885LMNA 4750/4885
US-20100185006-A1 NOVEL SIRTUIN ACTIVATING COMPOUNDS AND PROCESSES FOR MAKING THE SAME SIRT1, SIRT2, SIRT3 TTR 3825/4885MAPT 4298/4885LMNA 1305/4885
US-20160015733-A1 METHODS AND COMPOSITIONS FOR MODULATING TAU LEVELS MAPT, NEFM, PSEN2 TTR 38/4885MAPT 1/4885LMNA 761/4885
US-20080255382-A1 N-heterocyclic carbon-type ligand coupling in the presence of a base with benzyol halide and styrene coupling partners; resveratrol; increased stability for use in the food, cosmetic and pharmaceutical industries RB1, SBK1, NADK TTR 2092/4885MAPT 4496/4885LMNA 1421/4885

“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.

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