10-O-Methylhostasine

Details

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Internal ID 2c7b202b-c59c-465a-8c30-4f0cb3a945ce
Taxonomy Alkaloids and derivatives > Amaryllidaceae alkaloids > Homolycorine-type amaryllidaceae alkaloids
IUPAC Name (3R,5'S,6'R,7'aR)-5',6'-dihydroxy-5,6,7-trimethoxy-1'-methylspiro[2-benzofuran-3,7'-3,5,6,7a-tetrahydro-2H-indole]-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H23NO7/c1-20-6-5-9-7-11(21)17(22)19(16(9)20)10-8-12(24-2)14(25-3)15(26-4)13(10)18(23)27-19/h7-8,11,16-17,21-22H,5-6H2,1-4H3/t11-,16+,17+,19+/m0/s1
InChI Key ARKFTBZTMGGQCK-GIYVSIDVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H23NO7
Molecular Weight 377.40 g/mol
Exact Mass 377.14745207 g/mol
Topological Polar Surface Area (TPSA) 97.70 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.44
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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(3R,5'S,6'R,7'aR)-5',6'-dihydroxy-5,6,7-trimethoxy-1'-methylspiro(2-benzofuran-3,7'-3,5,6,7a-tetrahydro-2H-indole)-1-one
(3R,5'S,6'R,7'aR)-5',6'-dihydroxy-5,6,7-trimethoxy-1'-methylspiro[2-benzofuran-3,7'-3,5,6,7a-tetrahydro-2H-indole]-1-one
RefChem:77604
CHEMBL250688
BDBM50221067

2D Structure

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2D Structure of 10-O-Methylhostasine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8194 81.94%
Caco-2 + 0.7082 70.82%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5138 51.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9132 91.32%
OATP1B3 inhibitior + 0.9395 93.95%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4542 45.42%
P-glycoprotein inhibitior - 0.5644 56.44%
P-glycoprotein substrate - 0.6654 66.54%
CYP3A4 substrate + 0.6438 64.38%
CYP2C9 substrate - 0.8063 80.63%
CYP2D6 substrate + 0.4108 41.08%
CYP3A4 inhibition - 0.8558 85.58%
CYP2C9 inhibition - 0.7920 79.20%
CYP2C19 inhibition - 0.8130 81.30%
CYP2D6 inhibition - 0.7676 76.76%
CYP1A2 inhibition - 0.8091 80.91%
CYP2C8 inhibition - 0.7772 77.72%
CYP inhibitory promiscuity - 0.8139 81.39%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Danger 0.4949 49.49%
Eye corrosion - 0.9864 98.64%
Eye irritation - 0.9396 93.96%
Skin irritation - 0.7544 75.44%
Skin corrosion - 0.9254 92.54%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5654 56.54%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8292 82.92%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.6570 65.70%
Acute Oral Toxicity (c) III 0.5019 50.19%
Estrogen receptor binding + 0.5499 54.99%
Androgen receptor binding + 0.6331 63.31%
Thyroid receptor binding + 0.5185 51.85%
Glucocorticoid receptor binding + 0.7758 77.58%
Aromatase binding + 0.5449 54.49%
PPAR gamma + 0.6446 64.46%
Honey bee toxicity - 0.7777 77.77%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9541 95.41%

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%
CHEMBL4208 P20618 Proteasome component C5 96.89% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.50% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.83% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.01% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.78% 94.00%
CHEMBL2581 P07339 Cathepsin D 91.23% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.19% 96.77%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.26% 97.14%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 87.90% 82.38%
CHEMBL261 P00915 Carbonic anhydrase I 87.50% 96.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.30% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.20% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.79% 91.07%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.13% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.45% 90.71%
CHEMBL3820 P35557 Hexokinase type IV 81.57% 91.96%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.04% 92.62%

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.
Hosta plantaginea

Cross-Links

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PubChem 23642826
LOTUS LTS0172467
wikiData Q104917392