SCHEMBL517001

SCHEMBL517001

C[C@@H](O)[C@H](O)c1ccccc1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KDM4E B2RXH2 3/20 0.65
▸ LMNA P02545 3/20 0.65
▸ ADRA2C P18825 2/20 0.65
▸ ADRA2A P08913 1/20 0.65
▸ HIF1A Q16665 1/20 0.65
▸ ALDH1A1 P00352 3/20 0.62
▸ TSHR P16473 2/20 0.60
▸ CHRM2 P08172 1/20 0.60
▸ ADRA1A P35348 1/20 0.60
▸ RGS12 O14924 1/20 0.60
▸ GLA P06280 1/20 0.60
▸ CYP3A4 P08684 1/20 0.60
▸ CYP2D6 P10635 1/20 0.60
▸ CYP2C9 P11712 1/20 0.60
▸ PKM P14618 1/20 0.60
▸ ALOX15 P16050 1/20 0.60
▸ ALOX12 P18054 1/20 0.60
▸ NFKB1 P19838 1/20 0.60
▸ HTR2A P28223 1/20 0.60
▸ CYP2C19 P33261 1/20 0.60

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
SCHEMBL12761516 1.00 KDM4E (0.65) KDM4ELMNAADRA2CADRA2AHIF1A
SCHEMBL6543382 1.00 KDM4E (0.65) KDM4ELMNAADRA2CADRA2AHIF1A
SCHEMBL28117044 1.00 KDM4E (0.65) KDM4ELMNAADRA2CADRA2AHIF1A
SCHEMBL5353745 1.00 KDM4E (0.65) KDM4ELMNAADRA2CADRA2AHIF1A
SCHEMBL1954690 1.00 KDM4E (0.65) KDM4ELMNAADRA2CADRA2AHIF1A
SCHEMBL25159 1.00 KDM4E (0.65) KDM4ELMNAADRA2CADRA2AHIF1A
SCHEMBL6483432 1.00 KDM4E (0.65) KDM4ELMNAADRA2CADRA2AHIF1A
SCHEMBL6689612 1.00 KDM4E (0.65) KDM4ELMNAADRA2CADRA2AHIF1A
Bicarbonate SCHEMBL4901524 0.93 LMNA (0.58) KDM4ELMNAADRA2CADRA2AHIF1A
SCHEMBL28002029 0.93 KDM4E (0.58) KDM4ELMNAADRA2CADRA2AHIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9828548-B2 Liquid-crystal composition DIC CORPORATION (JP) 2017-11-28 — — US disclosed
US-9828548-B2 Liquid-crystal composition DIC CORPORATION (JP) 2017-11-28 — — US disclosed
US-9822307-B2 Liquid crystalline medium and liquid crystal display MERCK PATENT GMBH (DE) 2017-11-21 — — US disclosed
US-9822307-B2 Liquid crystalline medium and liquid crystal display MERCK PATENT GMBH (DE) 2017-11-21 — — US disclosed
US-9789118-B2 Bicyclic acetyl-CoA carboxylase inhibitors and uses thereof NOVARTIS AG (CH) 2017-10-17 — — US disclosed
US-9789118-B2 Bicyclic acetyl-CoA carboxylase inhibitors and uses thereof NOVARTIS AG (CH) 2017-10-17 — — US disclosed
US-9789118-B2 Bicyclic acetyl-CoA carboxylase inhibitors and uses thereof NOVARTIS AG (CH) 2017-10-17 — — US disclosed
US-9771517-B2 Liquid-crystal optical modulation element DIC CORPORATION (JP) 2017-09-26 — — US disclosed
US-9771517-B2 Liquid-crystal optical modulation element DIC CORPORATION (JP) 2017-09-26 — — US disclosed
US-20160194561-A1 DIFLUOROPHENYL LIQUID CRYSTAL COMPOSITION DIC CORPORATION (JP) 2016-07-07 — — US disclosed
WO-2003080242-A1 SUPPORTED OSMATES, PROCESS FOR PREPARATION THEREOF, AND PROCESS FOR PREPARATION OF CHIRAL VICINAL DIOLS COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2003-10-02 — — WO disclosed
US-20030153794-A1 Process for the preparation of supported osmates COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH. 2003-08-14 — — US disclosed
US-20030105367-A1 Supported osmates, process for preparation thereof, and a process for the preparation of chiral vicinal diols using supported osmate catalyst COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2003-06-05 — — US disclosed
WO-2003035253-A1 PROCESS FOR THE PREPARATION OF SUPPORTED OSMATES COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2003-05-01 — — WO disclosed
US-6552234-B1 Reacting potassium osmate with such as quaternary ammonium divinylbenzene-styrene copolymer COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2003-04-22 — — US disclosed
US-6472570-B1 Method for the asymmetric dihydroxylation of olefins, using osmium catalysts BAYER AKTIENGESELLSCHAFT (DE) 2002-10-29 — — US disclosed
EP-1209142-A1 Preparation of new layered double hydroxides exchanged with osmate for asymmetric dihydroxylation of olefins to vicinal diols COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2002-05-29 — — EP disclosed
US-6387033-B1 CIS ISOMERS FOR HYDROXYLATION OF OLEFINS COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2002-05-14 — — US disclosed
EP-1175379-A1 METHOD FOR THE ASYMMETRIC DIHYDROXYLATION OF OLEFINS, USING OSMIUM CATALYSTS Bayer Aktiengesellschaft (DE) 2002-01-30 — — EP disclosed
WO-2000064844-A1 METHOD FOR THE ASYMMETRIC DIHYDROXYLATION OF OLEFINS, USING OSMIUM CATALYSTS BAYER AKTIENGESELLSCHAFT (DE) 2000-11-02 — — WO disclosed
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