Angustine

Details

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Internal ID 47c76737-c0d5-4bec-9b4d-69ab88c11835
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name 19-ethenyl-3,13,17-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15(20),16,18-octaen-14-one
SMILES (Canonical) C=CC1=CN=CC2=C1C=C3C4=C(CCN3C2=O)C5=CC=CC=C5N4
SMILES (Isomeric) C=CC1=CN=CC2=C1C=C3C4=C(CCN3C2=O)C5=CC=CC=C5N4
InChI InChI=1S/C20H15N3O/c1-2-12-10-21-11-16-15(12)9-18-19-14(7-8-23(18)20(16)24)13-5-3-4-6-17(13)22-19/h2-6,9-11,22H,1,7-8H2
InChI Key FACXQEOSOVJIPD-UHFFFAOYSA-N
Popularity 28 references in papers

Physical and Chemical Properties

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Molecular Formula C20H15N3O
Molecular Weight 313.40 g/mol
Exact Mass 313.121512110 g/mol
Topological Polar Surface Area (TPSA) 49.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.74
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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40041-96-1
ACon1_001438
C09032
19-ethenyl-3,13,17-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15(20),16,18-octaen-14-one
Indolo(2',3':3,4)pyrido(1,2-b)(2,7)naphthyridin-5(7H)-one, 1-ethenyl-8,13-dihydro-
AC1L9C1T
Angustin
SureCN2953015
CHEBI:2725
SCHEMBL2953015
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Angustine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.6763 67.63%
Blood Brain Barrier + 0.8679 86.79%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8234 82.34%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.8831 88.31%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior + 0.6295 62.95%
BSEP inhibitior + 0.7413 74.13%
P-glycoprotein inhibitior - 0.6791 67.91%
P-glycoprotein substrate - 0.8447 84.47%
CYP3A4 substrate + 0.5955 59.55%
CYP2C9 substrate - 0.6193 61.93%
CYP2D6 substrate - 0.8206 82.06%
CYP3A4 inhibition + 0.7307 73.07%
CYP2C9 inhibition - 0.9194 91.94%
CYP2C19 inhibition - 0.8906 89.06%
CYP2D6 inhibition - 0.7941 79.41%
CYP1A2 inhibition + 0.7996 79.96%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.7292 72.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6531 65.31%
Eye corrosion - 0.9858 98.58%
Eye irritation - 0.9683 96.83%
Skin irritation - 0.7876 78.76%
Skin corrosion - 0.9547 95.47%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5115 51.15%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.8879 88.79%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.7089 70.89%
Acute Oral Toxicity (c) II 0.5292 52.92%
Estrogen receptor binding + 0.9063 90.63%
Androgen receptor binding - 0.5072 50.72%
Thyroid receptor binding + 0.6907 69.07%
Glucocorticoid receptor binding + 0.7601 76.01%
Aromatase binding + 0.7872 78.72%
PPAR gamma + 0.7439 74.39%
Honey bee toxicity - 0.7930 79.30%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.7363 73.63%

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
CHEMBL5697 Q9GZT9 Egl nine homolog 1 99.47% 93.40%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.11% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.50% 95.56%
CHEMBL255 P29275 Adenosine A2b receptor 95.57% 98.59%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.21% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.68% 98.95%
CHEMBL3310 Q96DB2 Histone deacetylase 11 92.38% 88.56%
CHEMBL1781 P11387 DNA topoisomerase I 90.31% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.05% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.59% 94.45%
CHEMBL5103 Q969S8 Histone deacetylase 10 89.57% 90.08%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.49% 89.00%
CHEMBL2535 P11166 Glucose transporter 88.09% 98.75%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 84.66% 96.42%
CHEMBL1978 P11511 Cytochrome P450 19A1 83.91% 91.76%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.72% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.63% 86.33%
CHEMBL2424504 P29375 Lysine-specific demethylase 5A 83.45% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 83.40% 91.49%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.31% 93.99%
CHEMBL2094121 P14867 GABA-A receptor; alpha-1/beta-3/gamma-2 83.07% 95.50%
CHEMBL4302 P08183 P-glycoprotein 1 82.87% 92.98%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.01% 93.81%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 80.66% 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.
Cephalanthus natalensis
Nauclea orientalis
Nauclea pobeguinii
Psychotria bahiensis
Strychnos johnsonii

Cross-Links

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PubChem 441983
LOTUS LTS0227533
wikiData Q27105783