Water

Water

SCHEMBL29135219

CCCCC(=O)C(=O)c1ccc(-c2ccccc2)cc1.O

nearest known ligand 0.77

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 20)

geneUniProtsupporting neighboursconfidence
HDAC3 known ✓ O15379 1/20 0.51
HDAC1 known ✓ Q13547 1/20 0.51
HDAC2 known ✓ Q92769 1/20 0.51
HDAC8 known ✓ Q9BY41 1/20 0.51
ALOX5 known ✓ P09917 1/20 0.46
DRD2 known ✓ P14416 1/20 0.46
DRD4 known ✓ P21917 1/20 0.46
DRD3 known ✓ P35462 1/20 0.46
CES2 O00748 5/20 0.77
CES1 P23141 5/20 0.77
SMN1; SMN2 Q16637 4/20 0.57
HPGD P15428 3/20 0.57
L3MBTL1 Q9Y468 2/20 0.57
POLB P06746 1/20 0.52
MAPT P10636 3/20 0.51
GAA P10253 1/20 0.51
NCOR2 Q9Y618 1/20 0.51
ALDH1A1 P00352 1/20 0.47
LTB4R2 Q9NPC1 1/20 0.47
RARB P10826 2/20 0.46

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
SCHEMBL7219046 0.88 CES1 (1.00) CES2CES1L3MBTL1MAPTALDH1A1
SCHEMBL7219754 0.82 CES2 (1.00) CES2CES1L3MBTL1MAPTLMNA
SCHEMBL15825890 0.81 CES2 (1.00) CES2CES1L3MBTL1MAPTLMNA
SCHEMBL28069086 0.81 CES2 (1.00) CES2CES1L3MBTL1MAPTLMNA
SCHEMBL9292210 0.81 CES2 (1.00) CES2CES1L3MBTL1MAPTLMNA
SCHEMBL2564081 0.81 CES2 (1.00) CES2CES1L3MBTL1MAPTLMNA
SCHEMBL6606979 0.81 L3MBTL1 (0.79) SMN1; SMN2HPGDL3MBTL1POLBMAPT
SCHEMBL29895716 0.81 CES2 (0.73) CES2CES1SMN1; SMN2HPGDL3MBTL1
SCHEMBL11664390 0.79 CES2 (0.93) CES2CES1L3MBTL1MAPTLMNA
SCHEMBL28578490 0.77 CES2 (0.79) CES2CES1L3MBTL1MAPTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117304233-A Iridium metal complex, application thereof and organic electroluminescent device 清华大学 2023-12-29 CN disclosed