3-Amino-4,5-dimethyl-2(5H)-furanone

Details

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Internal ID cd716c5a-ed64-459a-95f5-8ec16e89f3c0
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives
IUPAC Name 4-amino-2,3-dimethyl-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H9NO2/c1-3-4(2)9-6(8)5(3)7/h4H,7H2,1-2H3
InChI Key AFXUOKDSKBJSRH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C6H9NO2
Molecular Weight 127.14 g/mol
Exact Mass 127.063328530 g/mol
Topological Polar Surface Area (TPSA) 52.30 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.16
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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AFXUOKDSKBJSRH-UHFFFAOYSA-N
AKOS006337618

2D Structure

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2D Structure of 3-Amino-4,5-dimethyl-2(5H)-furanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 - 0.6113 61.13%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.6340 63.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9598 95.98%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9397 93.97%
P-glycoprotein inhibitior - 0.9763 97.63%
P-glycoprotein substrate - 0.9505 95.05%
CYP3A4 substrate - 0.7122 71.22%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8708 87.08%
CYP3A4 inhibition - 0.9734 97.34%
CYP2C9 inhibition - 0.8605 86.05%
CYP2C19 inhibition - 0.7536 75.36%
CYP2D6 inhibition - 0.9152 91.52%
CYP1A2 inhibition - 0.5721 57.21%
CYP2C8 inhibition - 0.9885 98.85%
CYP inhibitory promiscuity - 0.6262 62.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.3966 39.66%
Eye corrosion - 0.9264 92.64%
Eye irritation + 0.8904 89.04%
Skin irritation - 0.6956 69.56%
Skin corrosion - 0.9081 90.81%
Ames mutagenesis - 0.5937 59.37%
Human Ether-a-go-go-Related Gene inhibition - 0.7508 75.08%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.7728 77.28%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6030 60.30%
Estrogen receptor binding - 0.9203 92.03%
Androgen receptor binding - 0.7479 74.79%
Thyroid receptor binding - 0.8048 80.48%
Glucocorticoid receptor binding - 0.9328 93.28%
Aromatase binding - 0.7304 73.04%
PPAR gamma - 0.8660 86.60%
Honey bee toxicity - 0.8204 82.04%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity - 0.5918 59.18%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.51% 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.
Quararibea funebris

Cross-Links

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PubChem 6421106
LOTUS LTS0207135
wikiData Q104911625