SCHEMBL676889

SCHEMBL676889

CC(=O)/C=C/c1ccc(O)cc1O

nearest known ligand 0.64

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CHRNA7 P36544 7/20 0.64
TYR P14679 3/20 0.64
LMNA P02545 1/20 0.61
MAPT P10636 1/20 0.61
BACE1 P56817 1/20 0.58
IAPP P10997 1/20 0.53
SYNJ2 O15056 1/20 0.52
TTR P02766 1/20 0.52
CYP1A1 P04798 1/20 0.52
BCHE P06276 1/20 0.52
MMP2 P08253 1/20 0.52
ALOX5 P09917 1/20 0.52
PTPN1 P18031 1/20 0.52
PTGS1 P23219 1/20 0.52
CYP1B1 Q16678 1/20 0.52
PTPN22 Q9Y2R2 1/20 0.52

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
SCHEMBL1820391 1.00 CHRNA7 (0.64) CHRNA7TYRLMNAMAPTBACE1
SCHEMBL26601267 0.85 MAPT (0.67) CHRNA7LMNAMAPTBACE1IAPP
SCHEMBL4653701 0.84 CHRNA7 (0.68) CHRNA7TYRBACE1SYNJ2TTR
SCHEMBL4653698 0.84 CHRNA7 (0.68) CHRNA7TYRBACE1SYNJ2TTR
SCHEMBL18517696 0.83 MAPT (0.50) CHRNA7TYRLMNAMAPTBACE1
SCHEMBL89187 0.82 MIF (0.68) CHRNA7TYRBACE1
SCHEMBL28140874 0.82 MIF (0.68) CHRNA7TYRBACE1
SCHEMBL28391865 0.82 MIF (0.68) CHRNA7TYRBACE1
SCHEMBL471946 0.82 MIF (0.68) CHRNA7TYRBACE1
SCHEMBL26046386 0.82 TRIM24 (0.62) CHRNA7TYRLMNAMAPTBACE1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11746364-B2 Enzymatic synthesis of kavalactones and flavokavains WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH (US) 2023-09-05 US disclosed
US-11739354-B2 Enzymatic synthesis of kavalactones and flavokavains WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH (US) 2023-08-29 US disclosed
US-20220002768-A1 ENZYMATIC SYNTHESIS OF KAVALACTONES AND FLAVOKAVAINS WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH (US) 2022-01-06 US disclosed
US-20220002769-A1 ENZYMATIC SYNTHESIS OF KAVALACTONES AND FLAVOKAVAINS WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH (US) 2022-01-06 US disclosed
US-20190142940-A1 Method and system for effecting changes in pigmented tissue MOAZED KAMBIZ THOMAS (US) 2019-05-16 US disclosed
EP-2686369-B1 MULTIFUNCTIONAL SULFUR-CONTAINING POLYMERS, COMPOSITIONS THEREOF AND METHODS OF USE PRC DESOTO INT INC (US) 2018-12-19 EP disclosed
EP-2686370-B1 TERMINAL-MODIFIED DIFUNCTIONAL SULFUR-CONTAINING POLYMERS, COMPOSITIONS THEREOF AND METHODS OF USE PRC DESOTO INT INC (US) 2018-09-26 EP disclosed
US-9744237-B2 Method and system for effecting changes in pigmented tissue MOAZED KAMBIZ THOMAS (US) 2017-08-29 US disclosed
EP-2758453-B9 FLEXIBLE POLYAMINES, FLEXIBLE AMINE-TERMINATED ADDUCTS, COMPOSITIONS THEREOF AND METHODS OF USE PRC DESOTO INT INC (US) 2016-09-14 EP disclosed
US-9422467-B2 Flexible polyamines, flexible amine-terminated adducts, compositions thereof and methods of use PRC-DESOTO INTERNATIONAL, INC. (US) 2016-08-23 US disclosed
US-20110280909-A1 METHOD AND SYSTEM FOR EFFECTING CHANGES IN PIGMENTED TISSUE MOAZED KAMBIZ THOMAS (US) 2011-11-17 US disclosed
US-20110178313-A1 POLYSILOXANE COMPOUND AND METHOD OF PRODUCING THE SAME OOTAKE NOBUMASA 2011-07-21 US disclosed
US-7939617-B2 Silsesquioxane derivative; electronic material, optical material, optoelectronic material, paint, and primer. CHISSO CORPORATION (JP) 2011-05-10 US disclosed
WO-2010087983-A1 METHOD AND SYSTEM FOR EFFECTING CHANGES IN PIGMENTED TISSUE MOAZED KAMBIZ THOMAS (US) 2010-08-05 WO disclosed
US-20080171846-A1 Polysiloxane compound and method of producing the same JNC CORPORATION (JP) 2008-07-17 US disclosed
US-7319129-B2 Silsesquioxane derivative and process for producing the same CHISSO CORPORATION (JP) 2008-01-15 US disclosed
US-7053167-B2 Silsesquioxane derivative having functional group CHISSO CORPORATION (JP) 2006-05-30 US disclosed
US-20060089504-A1 Silsesquioxane derivative having functional group ITO KENYA 2006-04-27 US disclosed
US-20060052623-A1 Having two cyclotetrasiloxne rings connected by O-Si groups obtained through hydrolysis and condensation of trifunctional hydrolyzable silicon compounds; functionalization; fireproofing, thermostability, weathproofing, photostability, dielectric, hardness, strength and chemical resistance CHISSO CORPORATION (JP) 2006-03-09 US disclosed
US-20040068074-A1 Production process for silsesquioxane derivative having functional group and silsesquioxane derivative JNC CORPORATION (JP) 2004-04-08 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-20060052623-A1 Having two cyclotetrasiloxne rings connected by O-Si groups obtained through hydrolysis and condensation of trifunctional hydrolyzable silicon compounds; functionalization; fireproofing, thermostability, weathproofing, photostability, dielectric, hardness, strength and chemical resistance STS, PFAS, POLQ CHRNA7 1477/4885TYR 907/4885LMNA 2213/4885
US-20110178313-A1 POLYSILOXANE COMPOUND AND METHOD OF PRODUCING THE SAME RPS4X, POLR2A, MSL1 CHRNA7 2259/4885TYR 4823/4885LMNA 1175/4885
US-20060089504-A1 Silsesquioxane derivative having functional group SFXN1, STS, SRM CHRNA7 1646/4885TYR 294/4885LMNA 2228/4885

“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.