Water

Water

SCHEMBL4754409

N[C@@H](Cc1ccc([N+](=O)[O-])cc1)C(=O)O.O

nearest known ligand 0.59

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
PTGS1 known ✓ P23219 2/20 0.58
DPP4 known ✓ P27487 2/20 0.52
GRIK1 known ✓ P39086 1/20 0.50
GRIK2 known ✓ Q13002 1/20 0.50
EGFR known ✓ P00533 1/20 0.50
ADORA3 known ✓ P0DMS8 1/20 0.50
HTR2A known ✓ P28223 1/20 0.50
PTGS2 known ✓ P35354 1/20 0.50
SLC7A5 Q01650 3/20 0.59
ALPI P09923 1/20 0.58
PKM P14618 1/20 0.58
XIAP P98170 1/20 0.58
PTPRA P18433 1/20 0.52
DPP7 Q9UHL4 2/20 0.52
DPP8 Q6V1X1 1/20 0.52
DPP9 Q86TI2 1/20 0.52
MMP2 P08253 2/20 0.51
MC4R P32245 1/20 0.51
LOXL2 Q9Y4K0 1/20 0.50
TPH1 P17752 1/20 0.50

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 SCHEMBL4754408 1.00 SLC7A5 (0.59) SLC7A5PTGS1ALPIPKMXIAP
Water SCHEMBL8721103 1.00 SLC7A5 (0.59) SLC7A5PTGS1ALPIPKMXIAP
Water SCHEMBL7729304 1.00 SLC7A5 (0.59) SLC7A5PTGS1ALPIPKMXIAP
SCHEMBL26444 0.98 SLC7A5 (0.61) SLC7A5PTGS1ALPIPKMXIAP
SCHEMBL26443 0.98 SLC7A5 (0.61) SLC7A5PTGS1ALPIPKMXIAP
SCHEMBL437181 0.98 SLC7A5 (0.61) SLC7A5PTGS1ALPIPKMXIAP
SCHEMBL503312 0.98 SLC7A5 (0.61) SLC7A5PTGS1ALPIPKMXIAP
Hydrochloric Acid SCHEMBL22285084 0.97 SLC7A5 (0.59) SLC7A5PTGS1ALPIPKMXIAP
Hydrochloric Acid SCHEMBL2724117 0.97 SLC7A5 (0.59) SLC7A5PTGS1ALPIPKMXIAP
Hydrochloric Acid SCHEMBL8716271 0.97 SLC7A5 (0.59) SLC7A5PTGS1ALPIPKMXIAP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2008018090-A2 AN IMPROVED PROCESS FOR THE PREPARATION OF ZOLMITRIPTAN MATRIX LABORATORIES LTD (IN) 2008-02-14 WO claimed
EP-4081503-B1 A PROCESS FOR THE SYNTHESIS OF MELPHALAN INDENA SPA (IT) 2025-07-30 EP disclosed
WO-2025125353-A1 METHOD OF PREPARATION OF ZAVEGEPANT, SYNTHESIS INTERMEDIATES OF ZAVEGEPANT AND METHODS OF PREPARATION THEREOF MOEHS IBERICA, S.L. (ES) 2025-06-19 WO disclosed
EP-4425181-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTE Bertis Inc (KR) 2024-09-04 EP disclosed
US-12077484-B2 Process for the synthesis of melphalan INDENA S.P.A. (IT) 2024-09-03 US disclosed
WO-2024118602-A1 COMPOSITIONS AND METHODS FOR REDUCING IMMUNE INTOLERANCE AND TREATING AUTOIMMUNE DISORDERS LAPIX THERAPEUTICS, INC. (US) 2024-06-06 WO disclosed
US-20240173389-A1 Compositions and Methods For Reducing Immune Intolerance LAPIX THERAPEUTICS, INC. (US) 2024-05-30 US disclosed
CN-114845991-B Method for synthesizing melphalan 意迪那有限公司 2024-05-07 CN disclosed
EP-4304643-A1 COMPOSITIONS AND METHODS FOR REDUCING IMMUNE INTOLERANCE Lapix Therapeutics, Inc. (US) 2024-01-17 EP disclosed
US-11787761-B2 Process for the synthesis of Melphalan INDENA S.P.A. (IT) 2023-10-17 US disclosed
WO-1997036859-A1 PARA-SUBSTITUTED PHENYLPROPANOIC ACID DERIVATIVES AS INTEGRIN ANTAGONISTS G.D. SEARLE & CO. (US) 1997-10-09 WO disclosed
WO-1997027315-A1 COMBINATORIAL HYDROXYPROPYLAMINE LIBRARY PHARMACOPEIA, INC. (US) 1997-07-31 WO disclosed
EP-0751765-A4 SULFONAMIDE DERIVATIVES AND THEIR USE PHARMACOPEIA INC (US) 1997-05-28 EP disclosed
US-5618825-A ENZYME INHIBITORS; ANTICOAGULANTS; VISION DISORDERS PHARMACOPEIA, INC. (US) 1997-04-08 US disclosed
EP-0751765-A1 SULFONAMIDE DERIVATIVES AND THEIR USE PHARMACOPEIA, INC. (US) 1997-01-08 EP disclosed
EP-0728145-A1 ENDOTHELIN RECEPTOR ANTAGONISTS Ciba-Geigy Japan Limited (JP) 1996-08-28 EP disclosed
WO-1995024186-A1 SULFONAMIDE DERIVATIVES AND THEIR USE PHARMACOPEIA, INC. (US) 1995-09-14 WO disclosed
WO-1995012611-A1 ENDOTHELIN RECEPTOR ANTAGONISTS JAPAT LTD. (CH) 1995-05-11 WO disclosed
US-5391556-A Thrombin inhibitors KARL THOMAE GMBH (DE) 1995-02-21 US disclosed
EP-0555824-A1 N-alpha-arylsulfonylated benzimidazolylalaninamide derivatives, medicaments based thereon and process for their preparation Dr. Karl Thomae GmbH (DE) 1993-08-18 EP 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 (3 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-12077484-B2 Process for the synthesis of melphalan PAH, TYR, IL4I1 PTGS1 1458/4885DPP4 1580/4885GRIK1 4856/4885
US-20240173389-A1 Compositions and Methods For Reducing Immune Intolerance TST, HLA-DRB1, CD74 PTGS1 1164/4885DPP4 3208/4885GRIK1 1528/4885
US-11787761-B2 Process for the synthesis of Melphalan PAH, TYR, MARS1 PTGS1 1274/4885DPP4 1531/4885GRIK1 4855/4885

“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.