Longitubanine A

Details

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Internal ID 62f66a46-e480-47af-96bd-bc65d85d5f39
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Glutamine and derivatives
IUPAC Name 2-amino-5-[(3-methyl-2,5-dihydrofuran-2-yl)amino]-5-oxopentanoic acid
SMILES (Canonical) CC1=CCOC1NC(=O)CCC(C(=O)O)N
SMILES (Isomeric) CC1=CCOC1NC(=O)CCC(C(=O)O)N
InChI InChI=1S/C10H16N2O4/c1-6-4-5-16-9(6)12-8(13)3-2-7(11)10(14)15/h4,7,9H,2-3,5,11H2,1H3,(H,12,13)(H,14,15)
InChI Key NWUDALIQMUEQSX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16N2O4
Molecular Weight 228.24 g/mol
Exact Mass 228.11100700 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP -3.60
Atomic LogP (AlogP) -0.40
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Longitubanine A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6806 68.06%
Caco-2 - 0.7952 79.52%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5835 58.35%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9478 94.78%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.8231 82.31%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9360 93.60%
P-glycoprotein inhibitior - 0.9748 97.48%
P-glycoprotein substrate - 0.8542 85.42%
CYP3A4 substrate - 0.5389 53.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8337 83.37%
CYP3A4 inhibition - 0.9511 95.11%
CYP2C9 inhibition - 0.8708 87.08%
CYP2C19 inhibition - 0.8853 88.53%
CYP2D6 inhibition - 0.9270 92.70%
CYP1A2 inhibition - 0.8856 88.56%
CYP2C8 inhibition - 0.9175 91.75%
CYP inhibitory promiscuity - 0.9814 98.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6217 62.17%
Eye corrosion - 0.9829 98.29%
Eye irritation - 0.9879 98.79%
Skin irritation - 0.7738 77.38%
Skin corrosion - 0.8944 89.44%
Ames mutagenesis - 0.6054 60.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6553 65.53%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8849 88.49%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.6966 69.66%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.8871 88.71%
Acute Oral Toxicity (c) III 0.5879 58.79%
Estrogen receptor binding - 0.6145 61.45%
Androgen receptor binding - 0.7810 78.10%
Thyroid receptor binding - 0.7592 75.92%
Glucocorticoid receptor binding - 0.8414 84.14%
Aromatase binding - 0.7676 76.76%
PPAR gamma - 0.7036 70.36%
Honey bee toxicity - 0.9669 96.69%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.3930 39.30%

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 97.08% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.46% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.54% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 90.50% 90.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.51% 90.71%
CHEMBL2581 P07339 Cathepsin D 85.80% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.78% 97.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.39% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 84.00% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.90% 94.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.69% 93.56%
CHEMBL2514 O95665 Neurotensin receptor 2 80.99% 100.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.82% 97.21%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.06% 96.47%

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.
Hemerocallis fulva
Hemerocallis fulva var. angustifolia

Cross-Links

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PubChem 102377982
NPASS NPC202847
LOTUS LTS0019272
wikiData Q104400617