Xanthene

Xanthene

SCHEMBL6192065

O.c1ccc2c(c1)Cc1ccccc1O2

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Xanthene. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ALOX5 known ✓ P09917 1/20 0.40
HTR2A known ✓ P28223 1/20 0.37
MAOA P21397 3/20 0.94
MAOB P27338 2/20 0.94
GAA P10253 1/20 0.50
NPSR1 Q6W5P4 1/20 0.50
MAPKAPK2 P49137 1/20 0.47
NPC1 O15118 1/20 0.44
LMNA P02545 1/20 0.44
RAB9A P51151 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
ACSL1 P33121 1/20 0.41
ABCG2 Q9UNQ0 1/20 0.39
ITGB2 P05107 1/20 0.39
ICAM1 P05362 1/20 0.39
ITGAL P20701 1/20 0.39
OXTR P30559 1/20 0.38
CYP1A2 P05177 1/20 0.38

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
Xanthene SCHEMBL8797707 1.00 MAOA (0.94) MAOAMAOBGAANPSR1MAPKAPK2
Xanthene SCHEMBL11602030 0.97 MAOA (0.90) MAOAMAOBGAANPSR1MAPKAPK2
Xanthene SCHEMBL27884847 0.97 MAOA (0.90) MAOAMAOBGAANPSR1MAPKAPK2
Xanthene SCHEMBL28879157 0.97 MAOA (0.90) MAOAMAOBGAANPSR1MAPKAPK2
Xanthene SCHEMBL27493963 0.97 MAOA (1.00) MAOAMAOBGAANPSR1MAPKAPK2
Xanthene SCHEMBL4267 0.97 MAOA (1.00) MAOAMAOBGAANPSR1MAPKAPK2
Xanthene SCHEMBL30586075 0.97 MAOA (1.00) MAOAMAOBGAANPSR1MAPKAPK2
Xanthene SCHEMBL9339684 0.97 MAOA (1.00) MAOAMAOBGAANPSR1MAPKAPK2
Xanthene SCHEMBL29378346 0.97 MAOA (1.00) MAOAMAOBGAANPSR1MAPKAPK2
Xanthene SCHEMBL23355281 0.94 MAOA (0.94) MAOAMAOBGAANPSR1MAPKAPK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114085267-B Method for detecting ethyl carbamate 华南农业大学 2023-04-25 CN claimed
CN-114230632-B Acrylamide derivative mimic epitope peptide and application thereof 华南农业大学 2023-01-24 CN claimed
CN-114230632-A Acrylamide derivative mimic epitope peptide and application thereof 华南农业大学 2022-03-25 CN claimed
CN-114085267-A Method for detecting ethyl carbamate 华南农业大学 2022-02-25 CN claimed
CN-114107113-B Method for reducing ethyl carbamate in fermented food by using synthetic starter 江南大学 2023-07-18 CN disclosed
WO-2023093960-A1 MODIFIED PEPTIDE-OLIGONUCLEOTIDE CONJUGATE SYDDANSK UNIVERSITET (DK) 2023-06-01 WO disclosed
CN-114085267-B Method for detecting ethyl carbamate 华南农业大学 2023-04-25 CN disclosed
CN-113913314-B Strain for reducing accumulation of urea and ethyl carbamate in yellow wine and application thereof 江南大学 2023-02-24 CN disclosed
CN-114230632-B Acrylamide derivative mimic epitope peptide and application thereof 华南农业大学 2023-01-24 CN disclosed
CN-114230632-A Acrylamide derivative mimic epitope peptide and application thereof 华南农业大学 2022-03-25 CN disclosed
CN-114107113-A Method for reducing ethyl carbamate in fermented food by using synthetic leavening agent 江南大学 2022-03-01 CN disclosed
CN-114085267-A Method for detecting ethyl carbamate 华南农业大学 2022-02-25 CN disclosed
WO-1993004580-A1 N-(4-PYRIDYL OR 4-QUINOLINYL) ARYLACETAMIDE PESTICIDES DOWELANCO (US) 1993-03-18 WO disclosed
WO-1993005050-A1 4-(ARALKOXY OR ARALKYLAMINO)PYRIDINE PESTICIDES_________________ DOWELANCO (US) 1993-03-18 WO disclosed
WO-1993004579-A1 NEMATICIDAL USE OF 4-ARALKYLPYRIDINES DOWELANCO (US) 1993-03-18 WO disclosed
US-5137879-A Fungicide, miticide and insecticide DOWELANCO (US) 1992-08-11 US disclosed
US-5034393-A Fungicides for plants DOWELANCO (US) 1991-07-23 US disclosed
EP-0414386-A1 Condensed pyrimidine derivates DowElanco (US) 1991-02-27 EP disclosed
EP-0410762-A1 Naphthyridine derivatives DowElanco (US) 1991-01-30 EP disclosed
EP-0326329-A2 Quinazoline derivatives DowElanco (US) 1989-08-02 EP disclosed