3-Aminopentanedioic acid

Details

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Internal ID 91baf29b-c807-40c5-86dd-a614b1b1c247
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Amino fatty acids
IUPAC Name 3-aminopentanedioic acid
SMILES (Canonical) C(C(CC(=O)O)N)C(=O)O
SMILES (Isomeric) C(C(CC(=O)O)N)C(=O)O
InChI InChI=1S/C5H9NO4/c6-3(1-4(7)8)2-5(9)10/h3H,1-2,6H2,(H,7,8)(H,9,10)
InChI Key BBJIPMIXTXKYLZ-UHFFFAOYSA-N
Popularity 48 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9NO4
Molecular Weight 147.13 g/mol
Exact Mass 147.05315777 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP -3.90
Atomic LogP (AlogP) -0.74
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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1948-48-7
3-Aminoglutaric acid
beta-Glutamic acid
3-Aminoglutarate
Isoglutamic acid
Pentanedioic acid, 3-amino-
beta-Aminoglutaric acid
GLUTAMIC ACID, BETA
Isoglutamate
SFG5X9C3DQ
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Aminopentanedioic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6742 67.42%
Caco-2 - 0.7455 74.55%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4663 46.63%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.9784 97.84%
OATP1B3 inhibitior + 0.9382 93.82%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9718 97.18%
P-glycoprotein inhibitior - 0.9883 98.83%
P-glycoprotein substrate - 0.9917 99.17%
CYP3A4 substrate - 0.8205 82.05%
CYP2C9 substrate + 0.6180 61.80%
CYP2D6 substrate - 0.7526 75.26%
CYP3A4 inhibition - 0.9581 95.81%
CYP2C9 inhibition - 0.9618 96.18%
CYP2C19 inhibition - 0.9736 97.36%
CYP2D6 inhibition - 0.9486 94.86%
CYP1A2 inhibition - 0.9628 96.28%
CYP2C8 inhibition - 0.9949 99.49%
CYP inhibitory promiscuity - 0.9944 99.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.7249 72.49%
Eye corrosion - 0.9586 95.86%
Eye irritation + 0.9427 94.27%
Skin irritation - 0.8067 80.67%
Skin corrosion - 0.7361 73.61%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7703 77.03%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.9552 95.52%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6260 62.60%
Acute Oral Toxicity (c) III 0.5478 54.78%
Estrogen receptor binding - 0.9641 96.41%
Androgen receptor binding - 0.8585 85.85%
Thyroid receptor binding - 0.9105 91.05%
Glucocorticoid receptor binding - 0.7321 73.21%
Aromatase binding - 0.8539 85.39%
PPAR gamma - 0.9070 90.70%
Honey bee toxicity - 0.9221 92.21%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.9056 90.56%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.55% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 88.76% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.99% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 80.88% 90.20%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.54% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 80.28% 90.17%

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.
Anacyclus monanthos
Arum palaestinum
Astragalus siculus
Caulophyllum robustum
Corydalis balansae
Euphorbia cuneata
Guizotia scabra
Hakea trifurcata
Mikania cordifolia
Prunus speciosa
Raoulia australis
Senecio chionophilus
Terminalia brachystemma
Ulmus glabra

Cross-Links

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PubChem 73064
NPASS NPC27988
LOTUS LTS0039218
wikiData Q27103900