Iminodiacetic acid

Details

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Internal ID f190bc80-e9e8-4a86-9687-77f245bf27a2
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 2-(carboxymethylamino)acetic acid
SMILES (Canonical) C(C(=O)O)NCC(=O)O
SMILES (Isomeric) C(C(=O)O)NCC(=O)O
InChI InChI=1S/C4H7NO4/c6-3(7)1-5-2-4(8)9/h5H,1-2H2,(H,6,7)(H,8,9)
InChI Key NBZBKCUXIYYUSX-UHFFFAOYSA-N
Popularity 2,405 references in papers

Physical and Chemical Properties

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Molecular Formula C4H7NO4
Molecular Weight 133.10 g/mol
Exact Mass 133.03750770 g/mol
Topological Polar Surface Area (TPSA) 86.60 Ų
XlogP -3.30
Atomic LogP (AlogP) -1.25
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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142-73-4
2,2'-azanediyldiacetic acid
2,2'-Iminodiacetic acid
Glycine, N-(carboxymethyl)-
Aminodiacetic acid
Iminodiethanoic acid
N-(Carboxymethyl)glycine
Diglycocoll
Diglykokoll
Diglycin
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Iminodiacetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7234 72.34%
Caco-2 - 0.5149 51.49%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.4996 49.96%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.9481 94.81%
OATP1B3 inhibitior + 0.9537 95.37%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9883 98.83%
P-glycoprotein inhibitior - 0.9880 98.80%
P-glycoprotein substrate - 0.9907 99.07%
CYP3A4 substrate - 0.8264 82.64%
CYP2C9 substrate - 0.5814 58.14%
CYP2D6 substrate - 0.7810 78.10%
CYP3A4 inhibition - 0.9448 94.48%
CYP2C9 inhibition - 0.9594 95.94%
CYP2C19 inhibition - 0.9432 94.32%
CYP2D6 inhibition - 0.9573 95.73%
CYP1A2 inhibition - 0.9040 90.40%
CYP2C8 inhibition - 0.9933 99.33%
CYP inhibitory promiscuity - 0.9917 99.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7420 74.20%
Carcinogenicity (trinary) Non-required 0.7352 73.52%
Eye corrosion + 0.5191 51.91%
Eye irritation + 0.9931 99.31%
Skin irritation - 0.6669 66.69%
Skin corrosion - 0.8644 86.44%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8310 83.10%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8987 89.87%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.4613 46.13%
Acute Oral Toxicity (c) III 0.7343 73.43%
Estrogen receptor binding - 0.9779 97.79%
Androgen receptor binding - 0.9298 92.98%
Thyroid receptor binding - 0.9268 92.68%
Glucocorticoid receptor binding - 0.8655 86.55%
Aromatase binding - 0.8555 85.55%
PPAR gamma - 0.9297 92.97%
Honey bee toxicity - 0.9876 98.76%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.9373 93.73%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL221 P23219 Cyclooxygenase-1 92.79% 90.17%
CHEMBL4040 P28482 MAP kinase ERK2 88.09% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.48% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.37% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.41% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.06% 85.14%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Pogostemon cablin

Cross-Links

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PubChem 8897
NPASS NPC216443
LOTUS LTS0075590
wikiData Q409357