Agrostophyllin

Details

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Internal ID 2f5399a2-21dd-4a9e-8da4-f9c60a74b45b
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 5,13-dimethoxy-2-oxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,9,11,13-heptaen-6-ol
SMILES (Canonical) COC1=CC2=C3C(=C1)C=CC4=CC(=C(C(=C43)CO2)OC)O
SMILES (Isomeric) COC1=CC2=C3C(=C1)C=CC4=CC(=C(C(=C43)CO2)OC)O
InChI InChI=1S/C17H14O4/c1-19-11-5-9-3-4-10-6-13(18)17(20-2)12-8-21-14(7-11)16(9)15(10)12/h3-7,18H,8H2,1-2H3
InChI Key JUXGBQIIXCBKIW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H14O4
Molecular Weight 282.29 g/mol
Exact Mass 282.08920892 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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116174-99-3
5,13-dimethoxy-2-oxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4(16),5,7,9,11,13-heptaen-6-ol
CHEBI:2520
DTXSID30331910
Q27105700

2D Structure

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2D Structure of Agrostophyllin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9240 92.40%
Caco-2 + 0.8689 86.89%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6362 63.62%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.9278 92.78%
OATP1B3 inhibitior + 0.9869 98.69%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6180 61.80%
P-glycoprotein inhibitior - 0.8753 87.53%
P-glycoprotein substrate - 0.9209 92.09%
CYP3A4 substrate - 0.5662 56.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4944 49.44%
CYP3A4 inhibition - 0.5358 53.58%
CYP2C9 inhibition + 0.5811 58.11%
CYP2C19 inhibition + 0.8007 80.07%
CYP2D6 inhibition - 0.6857 68.57%
CYP1A2 inhibition + 0.9057 90.57%
CYP2C8 inhibition - 0.7455 74.55%
CYP inhibitory promiscuity + 0.6954 69.54%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6150 61.50%
Eye corrosion - 0.9826 98.26%
Eye irritation + 0.6948 69.48%
Skin irritation - 0.7301 73.01%
Skin corrosion - 0.9697 96.97%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5253 52.53%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8577 85.77%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7076 70.76%
Acute Oral Toxicity (c) III 0.5399 53.99%
Estrogen receptor binding + 0.8629 86.29%
Androgen receptor binding + 0.6606 66.06%
Thyroid receptor binding + 0.7089 70.89%
Glucocorticoid receptor binding + 0.6940 69.40%
Aromatase binding + 0.6583 65.83%
PPAR gamma + 0.6409 64.09%
Honey bee toxicity - 0.9348 93.48%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.7902 79.02%

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 98.85% 91.11%
CHEMBL4208 P20618 Proteasome component C5 93.38% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.93% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.94% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.79% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.77% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.08% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.52% 86.33%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.04% 92.68%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.90% 96.00%
CHEMBL2535 P11166 Glucose transporter 82.77% 98.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.96% 96.77%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.76% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.41% 95.56%

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.
Agrostophyllum brevipes
Agrostophyllum callosum

Cross-Links

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PubChem 442693
LOTUS LTS0005005
wikiData Q27105700