SCHEMBL2211027

SCHEMBL2211027

OC[C@@H](O)Cc1ccccc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TRPA1 O75762 3/20 0.56
CYP1A2 P05177 1/20 0.48
EPHX1 P07099 1/20 0.48
TSHR P16473 1/20 0.48
TRPV1 Q8NER1 1/20 0.47
SRR Q9GZT4 2/20 0.45
ALPI P09923 1/20 0.45
PKM P14618 1/20 0.45
PTGS1 P23219 1/20 0.45
XIAP P98170 1/20 0.45
SLC7A5 Q01650 1/20 0.45
SLC6A2 P23975 2/20 0.44
TAAR1 Q96RJ0 2/20 0.44
MAOA P21397 1/20 0.44
SLC6A4 P31645 1/20 0.44
SLC6A3 Q01959 1/20 0.44
SIGMAR1 Q99720 1/20 0.44
CYP2A6 P11509 1/20 0.44
ADORA2A P29274 1/20 0.44
ADORA1 P30542 1/20 0.44

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
SCHEMBL2212544 1.00 TRPA1 (0.56) TRPA1CYP1A2EPHX1TSHRTRPV1
SCHEMBL25158 1.00 TRPA1 (0.56) TRPA1CYP1A2EPHX1TSHRTRPV1
Hydrochloric Acid SCHEMBL28131666 0.98 TRPA1 (0.54) TRPA1CYP1A2EPHX1TSHRTRPV1
Dimethylamine SCHEMBL28101946 0.91 TRPA1 (0.53) TRPA1TRPV1SLC6A2TAAR1MAOA
SCHEMBL8752288 0.89 TRPA1 (0.50) TRPA1CYP1A2EPHX1TSHRTRPV1
SCHEMBL1833635 0.87 TRPA1 (0.55) TRPA1CYP1A2EPHX1TSHRTRPV1
Di(Hydroxyethyl)Ether SCHEMBL28301309 0.86 TRPA1 (0.45) TRPA1CYP1A2EPHX1TSHRTRPV1
Acrylic Acid SCHEMBL29037084 0.84 TRPA1 (0.51) TRPA1CYP1A2TRPV1SRRALPI
Ammonia Solution, Strong SCHEMBL29021310 0.84 TRPA1 (0.53) TRPA1CYP1A2EPHX1TSHRTRPV1
SCHEMBL10777895 0.83 TRPA1 (0.50) TRPA1TSHRPKMSLC6A2TAAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0589446-B1 N-(Hydroxyethyl)butanediamide derivatives as renin inhibitors BOEHRINGER INGELHEIM CA LTD (CA) 1997-09-03 EP claimed
EP-0317998-B1 Manufacturing method of optically-active 1,2-diols KANEGAFUCHI CHEMICAL IND (JP) 1994-08-31 EP claimed
US-4981796-A BIOSYNTHESIS KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1991-01-01 US claimed
EP-0317998-A2 Manufacturing method of optically-active 1,2-diols KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1989-05-31 EP claimed
EP-3681504-B1 METHODS OF DETECTION USING X-RAY FLUORESCENCE ICAGEN INC (US) 2023-08-23 EP disclosed
US-11573224-B2 Methods of detection using X-ray fluorescence ICAGEN, LLC (US) 2023-02-07 US disclosed
US-11446398-B2 Regulated biocircuit systems OBSIDIAN THERAPEUTICS, INC. (US) 2022-09-20 US disclosed
US-20210254056-A1 IDENTIFICATION AND TARGETED MODULATION OF GENE SIGNALING NETWORKS CAMP4 THERAPEUTICS CORPORATION 2021-08-19 US disclosed
US-10877035-B2 Advanced drug development and manufacturing ICAGEN, LLC (US) 2020-12-29 US disclosed
US-20200278346-A1 METHODS OF DETECTION USING X-RAY FLUORESCENCE ADJACENT ACQUISITION CO., LLC 2020-09-03 US disclosed
US-20190192691-A1 REGULATED BIOCIRCUIT SYSTEMS OBSIDIAN THERAPEUTICS, INC. 2019-06-27 US disclosed
US-20150309021-A1 Advanced Drug Development and Manufacturing LOS ALAMOS NATIONAL SECURITY, LLC 2015-10-29 US disclosed
US-20080220441-A1 Advanced drug development and manufacturing THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2008-09-11 US disclosed
EP-1175382-B1 METHOD FOR THE DIHYDROXYLATION OF OLEFINS USING TRANSITION-METAL CATALYSTS BAYER CHEMICALS AG (DE) 2005-02-09 EP disclosed
EP-0317998-B1 Manufacturing method of optically-active 1,2-diols KANEGAFUCHI CHEMICAL IND (JP) 1994-08-31 EP disclosed
US-4981796-A BIOSYNTHESIS KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1991-01-01 US disclosed
EP-0317998-A2 Manufacturing method of optically-active 1,2-diols KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1989-05-31 EP disclosed
EP-0031877-B1 OPTICALLY ACTIVE 1,2-BIS-(DIPHENYLPHOSPHINO)-COMPOUNDS, METAL COMPLEXES CONTAINING THEM AS CHIRAL LIGANDS AND THEIR USE Degussa Aktiengesellschaft (DE) 1983-02-02 EP disclosed
US-4356324-A CHIRAL LIGANDS FOR RHODIUM HYDROGENATION CATALYSTS DEGUSSA AKTIENGESELLSCHAFT, A GERMAN CORP. (DE) 1982-10-26 US disclosed
EP-0031877-A1 Optically active 1,2-Bis-(diphenylphosphino)-compounds, metal complexes containing them as chiral ligands and their use Degussa Aktiengesellschaft (DE) 1981-07-15 EP disclosed