Edetic Acid

Edetic Acid

SCHEMBL857218

O=C([O-])CN(CCN(CC(=O)[O-])CC(=O)[O-])CC(=O)[O-].[Fe+3].[K+]

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AGTR1DHFRGABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTNR3C2PBP2XPTGS1PTGS2VKORC1blablaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAftsImrcAmrcBmrdApbp1apbp1bpbp2apbp2bpbp3polthyA

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
KDM4E B2RXH2 2/20 0.65
ALOX15 P16050 2/20 0.65
MAPT P10636 1/20 0.65
SMN1; SMN2 Q16637 1/20 0.65
TDP1 Q9NUW8 2/20 0.48
EYA2 O00167 1/20 0.48
APP P05067 1/20 0.48
ACE P12821 1/20 0.48
BLM P54132 2/20 0.46
PMP22 Q01453 2/20 0.46
LMNA P02545 1/20 0.46
CHRM2 P08172 1/20 0.46
ADRA2A P08913 1/20 0.46
TSHR P16473 1/20 0.46
DRD1 P21728 1/20 0.46
SLC6A2 P23975 1/20 0.46
SLC6A4 P31645 1/20 0.46
CYP2C19 P33261 1/20 0.46
ADRA1A P35348 1/20 0.46
DRD3 P35462 1/20 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
Edetic Acid SCHEMBL8401816 0.97 KDM4E (0.62) KDM4EALOX15MAPTSMN1; SMN2TDP1
Edetic Acid SCHEMBL9055511 0.97 KDM4E (0.68) KDM4EALOX15MAPTSMN1; SMN2TDP1
Edetic Acid SCHEMBL9054050 0.97 KDM4E (0.68) KDM4EALOX15MAPTSMN1; SMN2TDP1
Edetic Acid SCHEMBL120661 0.97 KDM4E (0.68) KDM4EALOX15MAPTSMN1; SMN2TDP1
Edetic Acid SCHEMBL1809230 0.97 KDM4E (0.68) KDM4EALOX15MAPTSMN1; SMN2TDP1
Edetic Acid SCHEMBL29351646 0.97 KDM4E (0.68) KDM4EALOX15MAPTSMN1; SMN2TDP1
Edetic Acid SCHEMBL1123289 0.97 KDM4E (0.68) KDM4EALOX15MAPTSMN1; SMN2TDP1
Edetic Acid SCHEMBL9054100 0.97 KDM4E (0.68) KDM4EALOX15MAPTSMN1; SMN2TDP1
Edetic Acid SCHEMBL65335 0.97 KDM4E (0.68) KDM4EALOX15MAPTSMN1; SMN2TDP1
Edetic Acid SCHEMBL3423511 0.94 KDM4E (0.65) KDM4EALOX15MAPTSMN1; SMN2TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4533440-A POTENTIAL DIFFERENCE BETWEEN REDOX AND REFERENCE ELECTRODES GENERAL ELECTRIC COMPANY (US) 1985-08-06 US claimed
US-20220193124-A1 Therapeutic Agent for Flavivirus Infection NEOPHARMA JAPAN CO., LTD (JP) 2022-06-23 US disclosed
EP-3960241-A1 THERAPEUTIC AGENT FOR FLAVIVIRUS INFECTION Neopharma Japan Co., Ltd. (JP) 2022-03-02 EP disclosed
CN-107001529-B Rheology modifier 巴斯夫欧洲公司 2020-08-25 CN disclosed
US-9163103-B2 Hydrophobically associating copolymers BASF SE (DE) 2015-10-20 US disclosed
US-9127125-B2 Process for preparing polyurethane-polyacrylate hybrid dispersions BASF SE (DE) 2015-09-08 US disclosed
US-20140316035-A1 HYDROPHOBICALLY ASSOCIATING COPOLYMERS BASF SE (DE) 2014-10-23 US disclosed
US-8783356-B2 Hydrophobically associating copolymers BASF SE (DE) 2014-07-22 US disclosed
CN-102439054-B Hydrophobically associating copolymers BASF SE 2014-05-21 CN disclosed
US-20130281636-A1 PROCESS FOR PREPARING POLYURETHANE-POLYACRYLATE HYBRID DISPERSIONS BASF SE (DE) 2013-10-24 US disclosed
EP-2432807-A2 HYDROPHOBICALLY ASSOCIATING COPOLYMERS BASF SE (DE) 2012-03-28 EP disclosed
US-20100331510-A1 HYDROPHOBICALLY ASSOCIATING COPOLYMERS BASF SE (DE) 2010-12-30 US disclosed
WO-2010133527-A2 HYDROPHOBICALLY ASSOCIATING COPOLYMERS BASF SE (DE) 2010-11-25 WO disclosed
EP-0573927-B1 Recycling method for photographic processing waste liquid KONISHIROKU PHOTO IND (JP) 2001-02-07 EP disclosed
US-5573895-A USING DISTILLATE AS SOLVENT KONICA CORPORATION (JP) 1996-11-12 US disclosed
EP-0471583-B1 Process for the preparation of salts of iron amino and hydroxy carboxylic acid complexes HAMPSHIRE CHEMICAL CORP (US) 1995-05-24 EP disclosed
EP-0590583-A1 Multi-part bleach-fix replenisher and use thereof in photographic processing EASTMAN KODAK COMPANY (US) 1994-04-06 EP disclosed
EP-0573927-A1 Recycling method for photographic processing waste liquid KONICA CORPORATION (JP) 1993-12-15 EP disclosed
US-5110965-A Iron chelates from magnetite W.R. GRACE & CO.-CONN. (US) 1992-05-05 US disclosed
EP-0471583-A1 Process for the preparation of salts of iron amino and hydroxy carboxylic acid complexes HAMPSHIRE CHEMICAL CORPORATION (US) 1992-02-19 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 (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-20220193124-A1 Therapeutic Agent for Flavivirus Infection ALAD, AADAT, AAAS KDM4E 1332/4885ALOX15 121/4885MAPT 863/4885

“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.