2-[(5R)-2-amino-4,5-dihydro-1H-imidazol-5-yl]acetic acid

Details

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Internal ID f7a96069-f838-48a0-89f9-679c040fc516
Taxonomy Organoheterocyclic compounds > Azoles > Imidazoles > Substituted imidazoles > Imidazolyl carboxylic acids and derivatives
IUPAC Name 2-[(5R)-2-amino-4,5-dihydro-1H-imidazol-5-yl]acetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H9N3O2/c6-5-7-2-3(8-5)1-4(9)10/h3H,1-2H2,(H,9,10)(H3,6,7,8)/t3-/m1/s1
InChI Key FJESSDHMDUSARB-GSVOUGTGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9N3O2
Molecular Weight 143.14 g/mol
Exact Mass 143.069476538 g/mol
Topological Polar Surface Area (TPSA) 87.70 Ų
XlogP -1.80
Atomic LogP (AlogP) -1.25
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[(5R)-2-amino-4,5-dihydro-1H-imidazol-5-yl]acetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9484 94.84%
Caco-2 - 0.5960 59.60%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.4515 45.15%
OATP2B1 inhibitior - 0.8553 85.53%
OATP1B1 inhibitior + 0.9692 96.92%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9650 96.50%
P-glycoprotein inhibitior - 0.9873 98.73%
P-glycoprotein substrate - 0.7859 78.59%
CYP3A4 substrate - 0.7132 71.32%
CYP2C9 substrate + 0.5862 58.62%
CYP2D6 substrate - 0.8294 82.94%
CYP3A4 inhibition - 0.9244 92.44%
CYP2C9 inhibition - 0.9548 95.48%
CYP2C19 inhibition - 0.9653 96.53%
CYP2D6 inhibition - 0.9147 91.47%
CYP1A2 inhibition - 0.9051 90.51%
CYP2C8 inhibition - 0.9676 96.76%
CYP inhibitory promiscuity - 1.0000 100.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5828 58.28%
Eye corrosion - 0.9839 98.39%
Eye irritation + 0.7324 73.24%
Skin irritation - 0.7573 75.73%
Skin corrosion - 0.8933 89.33%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7797 77.97%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8556 85.56%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8309 83.09%
Acute Oral Toxicity (c) III 0.5328 53.28%
Estrogen receptor binding - 0.8873 88.73%
Androgen receptor binding - 0.8624 86.24%
Thyroid receptor binding - 0.7947 79.47%
Glucocorticoid receptor binding - 0.6555 65.55%
Aromatase binding - 0.6038 60.38%
PPAR gamma - 0.7062 70.62%
Honey bee toxicity - 0.9749 97.49%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.9738 97.38%

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 97.33% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.99% 97.09%
CHEMBL2581 P07339 Cathepsin D 82.95% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.44% 95.56%

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.
Lactuca floridana
Scorzoneroides autumnalis

Cross-Links

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PubChem 55287481
NPASS NPC313104