Edetic Acid

Edetic Acid

SCHEMBL121983

O=C([O-])CN(CCN(CC(=O)[O-])CC(=O)O)CC(=O)[O-].O=C([O-])CN(CCN(CC(=O)[O-])CC(=O)O)CC(=O)[O-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+]

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Edetic Acid. 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
ACE known ✓ P12821 1/20 0.70
CA1 known ✓ P00915 16/20 0.45
CA2 known ✓ P00918 16/20 0.45
CA4 known ✓ P22748 6/20 0.45
CA12 known ✓ O43570 3/20 0.38
TDP1 Q9NUW8 2/20 0.70
EYA2 O00167 1/20 0.70
APP P05067 1/20 0.70
KDM4E B2RXH2 2/20 0.67
ALOX15 P16050 2/20 0.67
BLM P54132 2/20 0.67
PMP22 Q01453 2/20 0.67
LMNA P02545 1/20 0.67
CHRM2 P08172 1/20 0.67
ADRA2A P08913 1/20 0.67
TSHR P16473 1/20 0.67
DRD1 P21728 1/20 0.67
SLC6A2 P23975 1/20 0.67
SLC6A4 P31645 1/20 0.67
CYP2C19 P33261 1/20 0.67

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
Edetic Acid SCHEMBL2406173 1.00 TDP1 (0.70) TDP1EYA2APPACEKDM4E
Edetic Acid SCHEMBL6347089 1.00 TDP1 (0.70) TDP1EYA2APPACEKDM4E
Edetic Acid SCHEMBL49459 1.00 TDP1 (0.70) TDP1EYA2APPACEKDM4E
Edetic Acid SCHEMBL887881 1.00 TDP1 (0.70) TDP1EYA2APPACEKDM4E
Edetic Acid SCHEMBL5697081 1.00 TDP1 (0.70) TDP1EYA2APPACEKDM4E
Edetic Acid SCHEMBL6347093 1.00 TDP1 (0.70) TDP1EYA2APPACEKDM4E
Edetic Acid SCHEMBL7870390 1.00 TDP1 (0.70) TDP1EYA2APPACEKDM4E
Edetic Acid SCHEMBL59899 1.00 TDP1 (0.70) TDP1EYA2APPACEKDM4E
Edetic Acid SCHEMBL5305791 1.00 TDP1 (0.70) TDP1EYA2APPACEKDM4E
Edetic Acid SCHEMBL64648 1.00 TDP1 (0.70) TDP1EYA2APPACEKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2424374-A1 CLEANSER COMPOSITIONS AND METHODS FOR USING THE SAME Advanced Vision Research, Inc. (US) 2012-03-07 EP disclosed
WO-1989010114-A1 COMPOSITION FOR PROMOTING HAIR GROWTH IN ANDROGENETIC ALOPECIA AND METHOD THEREOF TRUSTEES OF BOSTON UNIVERSITY (US) 1989-11-02 WO disclosed
EP-0296205-A4 METHOD AND COMPOSITION FOR HAIR GROWTH IN COMMON PATTERN BALDNESS. UNIV BOSTON (US) 1989-03-14 EP disclosed
EP-0296205-A1 METHOD AND COMPOSITION FOR HAIR GROWTH IN COMMON PATTERN BALDNESS TRUSTEES OF BOSTON UNIVERSITY (US) 1988-12-28 EP disclosed
WO-1988004931-A1 METHOD AND COMPOSITION FOR HAIR GROWTH IN COMMON PATTERN BALDNESS TRUSTEES OF BOSTON UNIVERSITY (US) 1988-07-14 WO disclosed