Angustilodine

Details

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Internal ID 6b69ae60-7bdd-4d8d-b042-7ffdf4390893
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name methyl (1S,11S,12R,17S)-17-hydroxy-15-methyl-19-oxa-9,15-diazapentacyclo[9.6.3.02,10.03,8.012,17]icosa-2(10),3,5,7-tetraene-11-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24N2O4/c1-22-8-7-15-19(18(23)25-2)11-26-9-13(20(15,24)10-22)16-12-5-3-4-6-14(12)21-17(16)19/h3-6,13,15,21,24H,7-11H2,1-2H3/t13-,15-,19+,20-/m1/s1
InChI Key OQHUOBCAVFBTGK-NIJZUDBWSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24N2O4
Molecular Weight 356.40 g/mol
Exact Mass 356.17360725 g/mol
Topological Polar Surface Area (TPSA) 74.80 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.39
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Angustilodine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8732 87.32%
Caco-2 + 0.6046 60.46%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.7767 77.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9139 91.39%
OATP1B3 inhibitior + 0.9402 94.02%
MATE1 inhibitior - 0.8409 84.09%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4825 48.25%
P-glycoprotein inhibitior - 0.6398 63.98%
P-glycoprotein substrate + 0.6082 60.82%
CYP3A4 substrate + 0.6768 67.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4184 41.84%
CYP3A4 inhibition - 0.8308 83.08%
CYP2C9 inhibition - 0.9159 91.59%
CYP2C19 inhibition - 0.8567 85.67%
CYP2D6 inhibition - 0.8816 88.16%
CYP1A2 inhibition - 0.9351 93.51%
CYP2C8 inhibition - 0.5761 57.61%
CYP inhibitory promiscuity - 0.9416 94.16%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6272 62.72%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9881 98.81%
Skin irritation - 0.8119 81.19%
Skin corrosion - 0.9508 95.08%
Ames mutagenesis + 0.5630 56.30%
Human Ether-a-go-go-Related Gene inhibition - 0.3654 36.54%
Micronuclear + 0.6700 67.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8684 86.84%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 1.0000 100.00%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.8214 82.14%
Acute Oral Toxicity (c) III 0.5411 54.11%
Estrogen receptor binding + 0.5859 58.59%
Androgen receptor binding + 0.7264 72.64%
Thyroid receptor binding - 0.5752 57.52%
Glucocorticoid receptor binding + 0.6936 69.36%
Aromatase binding + 0.5794 57.94%
PPAR gamma + 0.6143 61.43%
Honey bee toxicity - 0.8388 83.88%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.7637 76.37%

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 98.22% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.05% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 95.99% 83.82%
CHEMBL2581 P07339 Cathepsin D 95.89% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.38% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.21% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.35% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.72% 85.14%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 88.94% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.08% 95.89%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 86.03% 94.08%
CHEMBL5028 O14672 ADAM10 85.98% 97.50%
CHEMBL3310 Q96DB2 Histone deacetylase 11 85.32% 88.56%
CHEMBL255 P29275 Adenosine A2b receptor 84.70% 98.59%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.66% 97.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.31% 94.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.16% 89.00%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 82.16% 89.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.97% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.91% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.87% 92.62%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.68% 94.23%

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 angustiloba

Cross-Links

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PubChem 101726897
LOTUS LTS0172091
wikiData Q105196832