SCHEMBL2632685

SCHEMBL2632685

COc1ccc(CCO)cc1O

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.71
CYP1A2 P05177 1/20 0.71
CYP3A4 P08684 1/20 0.71
NFKB1 P19838 1/20 0.71
LMNA P02545 2/20 0.69
MEN1 O00255 1/20 0.69
APEX1 P27695 1/20 0.69
KMT2A Q03164 1/20 0.69
TUBB4A P04350 5/20 0.67
TUBB P07437 5/20 0.67
TUBA3C P0DPH7 5/20 0.67
TUBA1B P68363 5/20 0.67
TUBA4A P68366 5/20 0.67
TUBB4B P68371 5/20 0.67
TUBB3 Q13509 5/20 0.67
TUBB2A Q13885 5/20 0.67
TUBB8 Q3ZCM7 5/20 0.67
TUBA3E Q6PEY2 5/20 0.67
TUBA1A Q71U36 5/20 0.67
TUBA1C Q9BQE3 5/20 0.67

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
SCHEMBL15535668 0.89 TUBB4A (0.69) TSHRCYP1A2CYP3A4NFKB1LMNA
SCHEMBL31527689 0.85 TUBB4A (0.68) TSHRCYP1A2CYP3A4NFKB1LMNA
SCHEMBL27183199 0.85 TUBB4A (0.68) TSHRCYP1A2CYP3A4NFKB1LMNA
SCHEMBL29833121 0.85 CYP3A4 (0.71) TSHRCYP1A2CYP3A4NFKB1LMNA
SCHEMBL901444 0.85 CYP3A4 (0.71) TSHRCYP1A2CYP3A4NFKB1LMNA
SCHEMBL30045575 0.85 TAAR1 (0.73) TSHRCYP3A4NFKB1LMNAGAA
SCHEMBL43681 0.85 TAAR1 (0.73) TSHRCYP3A4NFKB1LMNAGAA
SCHEMBL13098004 0.84 ATM (0.66) CYP1A2CYP3A4KMT2AKDM4EALDH1A1
SCHEMBL296593 0.84 ATM (0.66) CYP1A2CYP3A4KMT2AKDM4EALDH1A1
SCHEMBL347472 0.84 CYP1A2 (0.65) TSHRCYP1A2CYP3A4NFKB1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111343993-B Homovanillyl alcohol (HVA), HVA isomers, methods of making compositions comprising such compounds, and methods of using such compounds 雀巢产品有限公司 2024-03-29 CN claimed
CN-102860999-B 1-deoxidation-D-xylulose5-phosphoric acid reduction isomerization enzyme inhibitor and preparation method thereof UNIV NORTHWESTERN 2014-04-09 CN claimed
CN-102860999-A 1-deoxidation-D-xylulose5-phosphoric acid reduction isomerization enzyme inhibitor and preparation method thereof UNIV NORTHWESTERN 2013-01-09 CN claimed
US-20250287976-A1 COMPOSITIONS AND METHODS USING AT LEAST ONE OF OLEUROPEIN OR A METABOLITE THEREOF TO TREAT OR PREVENT MUSCLE FATIGUE FROM EXERCISE AND/OR FOR RESISTANCE TO MUSCLE FATIGUE FROM EXERCISE NESTLE SA (CH) 2025-09-18 US disclosed
US-20250228794-A1 HOMOVANILLYL ALCOHOL (HVA), HVA ISOMER, METHODS OF MAKING COMPOSITIONS COMPRISING SUCH COMPOUNDS, AND METHODS USING SUCH COMPOUNDS NESTLE SA (CH) 2025-07-17 US disclosed
CN-119013029-A Compositions and methods for treating or preventing exercise-induced muscle fatigue and/or for combating exercise-induced muscle fatigue using at least one of oleuropein or a metabolite thereof 雀巢产品有限公司 2024-11-22 CN disclosed
EP-3997086-B1 TETRAHYDROISOQUINOLINE COMPOUNDS ALLINKY BIOPHARMA (ES) 2024-06-05 EP disclosed
CN-111343993-B Homovanillyl alcohol (HVA), HVA isomers, methods of making compositions comprising such compounds, and methods of using such compounds 雀巢产品有限公司 2024-03-29 CN disclosed
EP-3706759-B1 HOMOVANILLYL ALCOHOL (HVA), HVA ISOMER, METHODS OF MAKING COMPOSITIONS COMPRISING SUCH COMPOUNDS, AND METHODS USING SUCH COMPOUNDS NESTLE SA (CH) 2023-11-15 EP disclosed
WO-2023213780-A1 COMPOSITIONS AND METHODS USING AT LEAST ONE OF OLEUROPEIN OR A METABOLITE THEREOF TO TREAT OR PREVENT MUSCLE FATIGUE FROM EXERCISE AND/OR FOR RESISTANCE TO MUSCLE FATIGUE FROM EXERCISE Société des Produits Nestlé S.A. (CH) 2023-11-09 WO disclosed
US-20230255238-A2 COMPOSITIONS AND METHODS USING AT LEAST ONE OF OLEUROPEIN OR A METABOLITE THEREOF TO TREAT OR PREVENT MUSCLE FATIGUE FROM EXERCISE AND/OR FOR RESISTANCE TO MUSCLE FATIGUE FROM EXERCISE NESTLE SA (CH) 2023-08-17 US disclosed
WO-2002011732-A1 NOVEL BICYCLIC AND TRICYCLIC PYRROLIDINE DERIVATIVES AS GNRH ANTAGONISTS GLAXO GROUP LIMITED (GB) 2002-02-14 WO disclosed
EP-0939749-A1 PROCESS FOR THE PREPARATION OF BENZYL-ETHERS Agro-Chemie Növenyvedöszer Gyárto Ertékesito Es Forgalmazo KFT. (HU) 1999-09-08 EP disclosed
WO-1998022416-A1 PROCESS FOR THE PREPARATION OF BENZYL-ETHERS AGRO-CHEMIE NÖVÉNYVÉDÖSZER GYÁRTÓ ÉRTÉKESITÓ ÉS FORGALMAZÓ KFT. (HU) 1998-05-28 WO disclosed
US-5534626-A SELECTIVE MUSCARINIC RECEPTOR ANTAGONIST INTERMEDIATES PFIZER INC. (US) 1996-07-09 US disclosed
US-5410046-A Selective muscarinic receptor antagonists PFIZER INC. (US) 1995-04-25 US disclosed
US-5231104-A Anticholinergic PFIZER INC. (US) 1993-07-27 US disclosed
EP-0350309-B1 PIPERIDINE DERIVATIVES Pfizer Limited (GB) 1992-11-11 EP disclosed
US-5089505-A Anticholinergic agents PFIZER INC. (US) 1992-02-18 US disclosed
EP-0350309-A1 Piperidine derivatives Pfizer Limited (GB) 1990-01-10 EP disclosed