Alpneumine F

Details

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Internal ID 58e7a769-0e1a-4caf-b886-e566779f1e53
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name methyl (2R,3S,9S,10S,13S)-10-hydroxy-11-oxa-6,15-diazahexacyclo[12.7.0.02,6.03,10.09,13.016,21]henicosa-1(14),16,18,20-tetraene-13-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H22N2O4/c1-25-18(23)19-10-26-20(24)12-6-8-22(9-7-14(19)20)16(12)15-11-4-2-3-5-13(11)21-17(15)19/h2-5,12,14,16,21,24H,6-10H2,1H3/t12-,14-,16+,19-,20+/m0/s1
InChI Key ASELQGFIWGKGJJ-KCFDGDNXSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H22N2O4
Molecular Weight 354.40 g/mol
Exact Mass 354.15795719 g/mol
Topological Polar Surface Area (TPSA) 74.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.69
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEMBL1165402
BDBM50321284

2D Structure

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2D Structure of Alpneumine F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9072 90.72%
Caco-2 + 0.5382 53.82%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.5270 52.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8935 89.35%
OATP1B3 inhibitior + 0.9369 93.69%
MATE1 inhibitior - 0.7828 78.28%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6784 67.84%
P-glycoprotein inhibitior - 0.7675 76.75%
P-glycoprotein substrate + 0.6187 61.87%
CYP3A4 substrate + 0.6735 67.35%
CYP2C9 substrate - 0.8042 80.42%
CYP2D6 substrate - 0.6596 65.96%
CYP3A4 inhibition - 0.5116 51.16%
CYP2C9 inhibition - 0.8291 82.91%
CYP2C19 inhibition - 0.8000 80.00%
CYP2D6 inhibition - 0.8242 82.42%
CYP1A2 inhibition - 0.7920 79.20%
CYP2C8 inhibition + 0.4865 48.65%
CYP inhibitory promiscuity - 0.8111 81.11%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6002 60.02%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.9875 98.75%
Skin irritation - 0.7937 79.37%
Skin corrosion - 0.9419 94.19%
Ames mutagenesis + 0.5330 53.30%
Human Ether-a-go-go-Related Gene inhibition - 0.4091 40.91%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8646 86.46%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.6415 64.15%
Acute Oral Toxicity (c) III 0.5085 50.85%
Estrogen receptor binding + 0.7154 71.54%
Androgen receptor binding + 0.7035 70.35%
Thyroid receptor binding - 0.5648 56.48%
Glucocorticoid receptor binding + 0.7570 75.70%
Aromatase binding + 0.5507 55.07%
PPAR gamma + 0.5569 55.69%
Honey bee toxicity - 0.8097 80.97%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7132 71.32%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.47% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.18% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.62% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.54% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.27% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.13% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.03% 99.23%
CHEMBL4040 P28482 MAP kinase ERK2 88.13% 83.82%
CHEMBL5028 O14672 ADAM10 86.50% 97.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.83% 92.62%
CHEMBL255 P29275 Adenosine A2b receptor 83.63% 98.59%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 83.19% 96.39%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.73% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.62% 97.09%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 82.18% 97.50%
CHEMBL2535 P11166 Glucose transporter 81.59% 98.75%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.30% 94.08%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.30% 92.94%
CHEMBL340 P08684 Cytochrome P450 3A4 80.85% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.48% 95.89%

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.
Alstonia pneumatophora

Cross-Links

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PubChem 46906305
LOTUS LTS0121683
wikiData Q104917776