Water

Water

SCHEMBL1093471

O.O.O=C(O)c1ccc(C(F)(c2ccc(C(=O)O)c(C(=O)O)c2)C(F)(F)C(F)(F)F)cc1C(=O)O

nearest known ligand 0.46

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

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

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 3/20 0.46
KDM4E B2RXH2 2/20 0.46
ALDH1A1 P00352 2/20 0.46
HPGD P15428 2/20 0.46
TDP1 Q9NUW8 1/20 0.41
USP2 O75604 1/20 0.41
CYP2C19 P33261 1/20 0.41
SORT1 Q99523 13/20 0.40
RXRA P19793 1/20 0.37
RXRB P28702 1/20 0.37
CES2 O00748 2/20 0.37
CDC25A P30304 1/20 0.37
CDC25B P30305 1/20 0.37

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
SCHEMBL829980 0.98 HSD17B10 (0.47) HSD17B10KDM4EALDH1A1HPGDTDP1
SCHEMBL28722893 0.85 RXRB (0.44) HSD17B10KDM4EALDH1A1HPGDUSP2
SCHEMBL8923161 0.84 HSD17B10 (0.47) HSD17B10KDM4EALDH1A1HPGDTDP1
SCHEMBL8676346 0.84 HSD17B10 (0.47) HSD17B10KDM4EALDH1A1HPGDTDP1
SCHEMBL28359746 0.83 ALDH1A1 (0.70) HSD17B10KDM4EALDH1A1HPGDTDP1
SCHEMBL8920312 0.82 HSD17B10 (0.46) HSD17B10KDM4EALDH1A1HPGDTDP1
Water SCHEMBL3223306 0.81 HSD17B10 (0.49) HSD17B10KDM4EALDH1A1HPGDTDP1
Water SCHEMBL4580188 0.81 HSD17B10 (0.49) HSD17B10KDM4EALDH1A1HPGDTDP1
SCHEMBL11338178 0.81 POLB (0.52) HSD17B10KDM4EALDH1A1HPGDTDP1
SCHEMBL31525219 0.81 POLB (0.52) HSD17B10KDM4EALDH1A1HPGDTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2239601-B1 LIGHT CONTROL FILM COMPRISING A PRIMER LAYER FORMED BY USING A PHOSPHORIC ESTER HITACHI CHEMICAL CO LTD (JP) 2017-11-08 EP disclosed
US-8154791-B2 Light control film HITACHI CHEMICAL COMPANY, LTD. (JP) 2012-04-10 US disclosed
US-20100309544-A1 LIGHT CONTROL FILM GAUZY LTD (IL) 2010-12-09 US disclosed