Homostephanoline

Details

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Internal ID 0a48becd-96b5-4bb1-8b06-d8bb78a2e450
Taxonomy Alkaloids and derivatives > Hasubanan alkaloids
IUPAC Name 4-hydroxy-3,11,12-trimethoxy-17-methyl-17-azatetracyclo[8.4.3.01,10.02,7]heptadeca-2(7),3,5,11-tetraen-13-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H25NO5/c1-21-10-9-19-11-14(23)17(25-3)18(26-4)20(19,21)8-7-12-5-6-13(22)16(24-2)15(12)19/h5-6,22H,7-11H2,1-4H3
InChI Key VCOZOQJXGDDART-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H25NO5
Molecular Weight 359.40 g/mol
Exact Mass 359.17327290 g/mol
Topological Polar Surface Area (TPSA) 68.20 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.14
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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SCHEMBL30723113
VCOZOQJXGDDART-UHFFFAOYSA-N
3-Hydroxy-4,7,8-trimethoxy-17-methyl-7,8-didehydrohasubanan-6-one #

2D Structure

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2D Structure of Homostephanoline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9805 98.05%
Caco-2 + 0.9116 91.16%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6372 63.72%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.9382 93.82%
OATP1B3 inhibitior + 0.9362 93.62%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.6946 69.46%
P-glycoprotein inhibitior - 0.7889 78.89%
P-glycoprotein substrate - 0.6473 64.73%
CYP3A4 substrate + 0.6295 62.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4013 40.13%
CYP3A4 inhibition - 0.8014 80.14%
CYP2C9 inhibition - 0.9320 93.20%
CYP2C19 inhibition - 0.8642 86.42%
CYP2D6 inhibition - 0.6129 61.29%
CYP1A2 inhibition - 0.8377 83.77%
CYP2C8 inhibition - 0.8933 89.33%
CYP inhibitory promiscuity - 0.8999 89.99%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5380 53.80%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.9303 93.03%
Skin irritation - 0.7879 78.79%
Skin corrosion - 0.9414 94.14%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4787 47.87%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.8544 85.44%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.6085 60.85%
Acute Oral Toxicity (c) III 0.6290 62.90%
Estrogen receptor binding + 0.5491 54.91%
Androgen receptor binding + 0.7481 74.81%
Thyroid receptor binding + 0.5189 51.89%
Glucocorticoid receptor binding + 0.7042 70.42%
Aromatase binding - 0.5269 52.69%
PPAR gamma + 0.5249 52.49%
Honey bee toxicity - 0.8897 88.97%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9343 93.43%

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 97.55% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.95% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 96.13% 93.40%
CHEMBL2581 P07339 Cathepsin D 93.71% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.68% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.88% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.94% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 88.93% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.73% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.79% 99.15%
CHEMBL2535 P11166 Glucose transporter 85.62% 98.75%
CHEMBL2056 P21728 Dopamine D1 receptor 83.30% 91.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.53% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.42% 94.45%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.06% 80.78%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.03% 93.99%

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.
Santalum album
Stephania japonica

Cross-Links

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PubChem 627343
NPASS NPC260015
LOTUS LTS0016723
wikiData Q105283865