Water

Water

SCHEMBL537059

C[C@H]1c2cccc(O)c2C(O)=C2C(=O)[C@]3(O)C(=O)/C(=C(/N)O)C(=O)[C@@H](N(C)C)[C@@H]3[C@@H](O)[C@@H]21.O.O.[Cl-].[H+]

nearest known ligand 0.72

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
MMP7 known ✓ P09237 1/20 0.72
MMP8 known ✓ P22894 1/20 0.72
ADORA1 known ✓ P30542 1/20 0.72
ADRA1A known ✓ P35348 1/20 0.72
MMP13 known ✓ P45452 1/20 0.72
MEN1 known ✓ O00255 6/20 0.47
THRB known ✓ P10828 5/20 0.46
MMP2 P08253 1/20 0.72
MMP3 P08254 1/20 0.72
TDP1 Q9NUW8 10/20 0.70
USP2 O75604 6/20 0.70
HSD17B10 Q99714 6/20 0.70
HIF1A Q16665 3/20 0.70
TSHR P16473 1/20 0.70
KDM4E B2RXH2 9/20 0.69
L3MBTL1 Q9Y468 7/20 0.69
RECQL P46063 7/20 0.67
PLA2G1B P04054 1/20 0.67
ATG4B Q9Y4P1 1/20 0.67
HPGD P15428 7/20 0.47

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
Water SCHEMBL1649970 0.98 MMP2 (0.74) MMP2MMP3MMP7MMP8ADORA1
SCHEMBL40930 0.97 TDP1 (0.73) MMP2MMP3MMP7MMP8ADORA1
SCHEMBL4082631 0.97 TDP1 (0.73) MMP2MMP3MMP7MMP8ADORA1
SCHEMBL21014939 0.97 TDP1 (0.73) MMP2MMP3MMP7MMP8ADORA1
SCHEMBL4082642 0.97 TDP1 (0.73) MMP2MMP3MMP7MMP8ADORA1
SCHEMBL23005369 0.97 TDP1 (0.73) MMP2MMP3MMP7MMP8ADORA1
SCHEMBL1176275 0.97 TDP1 (0.73) MMP2MMP3MMP7MMP8ADORA1
Alcohol SCHEMBL14973542 0.97 KDM4E (0.72) MMP2MMP3MMP7MMP8ADORA1
SCHEMBL18610140 0.90 TDP1 (0.65) MMP2MMP3MMP7MMP8ADORA1
Water SCHEMBL29358570 0.83 MMP2 (1.00) MMP2MMP3MMP7MMP8ADORA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9227999-B2 Antimicrobial cationic peptides and formulations thereof CARRUS CAPITAL CORPORATION (CA) 2016-01-05 US claimed
CN-119950523-B Doxycycline hydrochloride and clavulanate potassium powder for aquatic products and preparation method and application thereof YANGTZE RIVER FISHERIES RESEARCH INSTITUTE CHINESE ACADEMY OF FISHERY SCIENCES (CN) 2026-05-26 CN disclosed
EP-3866826-B1 ANTIMICROBIAL PEPTIDES AND METHODS OF USING THE SAME RIPTIDE BIOSCIENCE INC (US) 2025-12-10 EP disclosed
CN-119979581-A Whole-cell biosensor for detecting tetracycline in environmental water body and application thereof 华东师范大学 2025-05-13 CN disclosed
CN-119950523-A Doxycycline hydrochloride and clavulanate potassium powder for aquatic products and preparation method and application thereof 中国水产科学研究院长江水产研究所 2025-05-09 CN disclosed
US-20240299291-A1 OPHTHALMIC PREPARATION ADMINISTERED BY EYE DROPS AND USED FOR PREVENTING AND TREATING DRY MACULAR DEGENERATION AND RETINAL LIGHT DAMAGE Chengdu Ruimu Biopharmaceuticals Co., Ltd. (CN) 2024-09-12 US disclosed
WO-2024186695-A2 IMMUNE CELL FUSION (ICF) AND USES THEREOF TRUSTEES OF BOSTON UNIVERSITY (US) 2024-09-12 WO disclosed
US-20240293462-A1 Immune Cell Fusion (ICF) and Uses Thereof TRUSTEES OF BOSTON UNIVERSITY 2024-09-05 US disclosed
US-12031977-B2 Ex vivo system for determining multiple drug-drug transporter interactions and methods of use thereof MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2024-07-09 US disclosed
US-20240209370-A1 METHODS OF MODULATING ALK Société des Produits Nestlé S.A. (CH) 2024-06-27 US disclosed
EP-0925308-B1 COMPOSITIONS AND METHODS FOR TREATING INFECTIONS USING ANALOGUES OF INDOLICIDIN MICROLOGIX BIOTECH INC (CA) 2002-06-05 EP disclosed
US-20020035061-A1 COMPOSITIONS AND METHODS FOR TREATING INFECTIONS USING CATIONIC PEPTIDES ALONE OR IN COMBINATION WITH ANTIBIOTICS BIOWEST THERAPEUTICS INC. (CA) 2002-03-21 US disclosed
EP-1174439-A2 Compositions and methods for treating infections using analogues of indolicidin Micrologix Biotech, Inc. (CA) 2002-01-23 EP disclosed
US-6180604-B1 Compositions and methods for treating infections using analogues of indolicidin MICROLOGIX BIOTECH INC. (CA) 2001-01-30 US disclosed
EP-0966481-A2 COMPOSITIONS AND METHODS FOR TREATING INFECTIONS USING CATIONIC PEPTIDES ALONE OR IN COMBINATION WITH ANTIBIOTICS Micrologix Biotech, Inc. (CA) 1999-12-29 EP disclosed
WO-1999065506-A2 CANCER THERAPY WITH INDOLICIDIN OR CATIONIC PEPTIDES AND THEIR POLYMER CONJUGATES MICROLOGIX BIOTECH INC. (CA) 1999-12-23 WO disclosed
EP-0925308-A2 COMPOSITIONS AND METHODS FOR TREATING INFECTIONS USING ANALOGUES OF INDOLICIDIN Micrologix Biotech, Inc. (CA) 1999-06-30 EP disclosed
WO-1998040401-A2 COMPOSITIONS AND METHODS FOR TREATING INFECTIONS USING CATIONIC PEPTIDES ALONE OR IN COMBINATION WITH ANTIBIOTICS MICROLOGIX BIOTECH INC. (CA) 1998-09-17 WO disclosed
WO-1998007745-A9 COMPOSITIONS AND METHODS FOR TREATING INFECTIONS USING ANALOGUES OF INDOLICIDIN 1998-04-23 WO disclosed
WO-1998007745-A2 COMPOSITIONS AND METHODS FOR TREATING INFECTIONS USING ANALOGUES OF INDOLICIDIN MICROLOGIX BIOTECH, INC. (CA) 1998-02-26 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20020035061-A1 COMPOSITIONS AND METHODS FOR TREATING INFECTIONS USING CATIONIC PEPTIDES ALONE OR IN COMBINATION WITH ANTIBIOTICS VIP, PEPD, PTMS MMP7 212/4885MMP8 44/4885ADORA1 4243/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.