SCHEMBL4620889

SCHEMBL4620889

O=C(OC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)c1cc(O)c(O)c(O)c1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AKR1B1 P15121 1/20 0.56
SLC28A3 Q9HAS3 3/20 0.49
TDP1 Q9NUW8 2/20 0.48
TMPRSS2 O15393 1/20 0.48
USP2 O75604 1/20 0.48
PDE5A O76074 1/20 0.48
CA1 P00915 1/20 0.48
CA2 P00918 1/20 0.48
HMGCR P04035 1/20 0.48
CYP1A2 P05177 1/20 0.48
LCK P06239 1/20 0.48
FYN P06241 1/20 0.48
HSPD1 P10809 1/20 0.48
CYP2C9 P11712 1/20 0.48
CA6 P23280 1/20 0.48
TBXAS1 P24557 1/20 0.48
MAPK3 P27361 1/20 0.48
MAPK1 P28482 1/20 0.48
HSPE1 P61604 1/20 0.48
MAPK14 Q16539 1/20 0.48

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
SCHEMBL1315483 1.00 AKR1B1 (0.56) AKR1B1SLC28A3TDP1TMPRSS2USP2
SCHEMBL13456979 1.00 AKR1B1 (0.56) AKR1B1SLC28A3TDP1TMPRSS2USP2
SCHEMBL4416998 1.00 AKR1B1 (0.56) AKR1B1SLC28A3TDP1TMPRSS2USP2
SCHEMBL22504483 1.00 AKR1B1 (0.56) AKR1B1SLC28A3TDP1TMPRSS2USP2
SCHEMBL1263104 1.00 AKR1B1 (0.56) AKR1B1SLC28A3TDP1TMPRSS2USP2
SCHEMBL16906157 1.00 AKR1B1 (0.56) AKR1B1SLC28A3TDP1TMPRSS2USP2
SCHEMBL11986810 1.00 AKR1B1 (0.56) AKR1B1SLC28A3TDP1TMPRSS2USP2
SCHEMBL5664342 0.89 EPHX2 (0.55) AKR1B1SLC28A3TMPRSS2USP2PDE5A
SCHEMBL11986813 0.89 SLC28A3 (0.50) AKR1B1SLC28A3TDP1MAPK1PTPN1
SCHEMBL28793347 0.89 TMPRSS2 (0.52) AKR1B1TMPRSS2USP2PDE5ACA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117362365-A Method for extracting galloyl glucopyranoside from Loropetalum chinense 江西省科学院生物资源研究所 2024-01-09 CN claimed
CN-117362365-B Method for extracting galloyl glucopyranoside from Loropetalum chinense 江西省科学院生物资源研究所 2026-01-30 CN disclosed
CN-117362365-B Method for extracting galloyl glucopyranoside from Loropetalum chinense 江西省科学院生物资源研究所 2026-01-30 CN disclosed
CN-119185154-A Additive for brightening skin color and fading color spots and application thereof 广州市悦锐生物科技有限公司 2024-12-27 CN disclosed
CN-117362365-A Method for extracting galloyl glucopyranoside from Loropetalum chinense 江西省科学院生物资源研究所 2024-01-09 CN disclosed
CN-117362365-A Method for extracting galloyl glucopyranoside from Loropetalum chinense 江西省科学院生物资源研究所 2024-01-09 CN disclosed
CN-117362365-A Method for extracting galloyl glucopyranoside from Loropetalum chinense 江西省科学院生物资源研究所 2024-01-09 CN disclosed
CN-111148503-B Composition for oral application comprising myrtle extract and fluoride salt 皮埃尔法布雷医药公司 2022-08-30 CN disclosed
CN-109393254-B Composition and method for improving insect immunity 彦臣生技药品股份有限公司 2022-06-21 CN disclosed
EP-3661482-B1 COMPOSITION COMPRISING A MYRTLE EXTRACT AND A FLUORIDE SALT FOR ORAL CARE APPLICATION PF MEDICAMENT (FR) 2021-09-22 EP disclosed
EP-3661482-A1 COMPOSITION COMPRISING A MYRTLE EXTRACT AND A FLUORINE SALT FOR ORAL APPLICATION Pierre Fabre Medicament (FR) 2020-06-10 EP disclosed
CN-111148503-A Composition for oral application comprising myrtle extract and fluoride salt 皮埃尔法布雷医药公司 2020-05-12 CN disclosed
WO-2019025622-A1 COMPOSITION COMPRISING A MYRTLE EXTRACT AND A FLUORINE SALT FOR ORAL APPLICATION PIERRE FABRE MEDICAMENT (FR) 2019-02-07 WO disclosed
CN-102337308-A Method for converting bergenin into special nitrogenous derivative by using penicillium UNIV YANGZHOU 2012-02-01 CN disclosed
US-20080269510-A1 New alpha-glucosidase inhibitors and antibacterial compounds from Myrtus communis L. INTERNATIONAL INSTITUTE OF CHEMICAL SCIENCES (PK) 2008-10-30 US disclosed
EP-1945237-A2 USE OF EXTRACTS OF MYRTLE AND OTHER MEDITERRANEAN PLANT SPECIES, AS ANTIMYCOTIC AGENT TOWARDS YEAST AND YEAST-LIKE MICROORGANISMS Romani, Annalisa (IT) 2008-07-23 EP disclosed
WO-2007046125-A2 USE OF EXTRACTS OF MYRTLE AND OTHER MEDITERRANEAN PLANT SPECIES, AS ANTIMYCOTIC AGENT TOWARDS YEAST AND YEAST-LIKE MICROORGANISMS ROMANI ANNALISA (IT) 2007-04-26 WO disclosed
EP-1363594-A1 COSMETIC FORMULATIONS CONTAINING FLAVONOID DERIVATIVES MERCK PATENT GmbH (DE) 2003-11-26 EP disclosed
WO-2002069926-A1 COSMETIC FORMULATIONS CONTAINING FLAVONOID DERIVATIVES MERCK PATENT GMBH (DE) 2002-09-12 WO disclosed