Diaporthein B

Details

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Internal ID 35bf98fd-5194-4f01-a4fd-2e00213edc60
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name (1S,3R,5R,9R,10R)-5-ethenyl-2,3,9,10-tetrahydroxy-5,11,11-trimethyl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadec-6-en-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H28O6/c1-5-16(4)9-12-14(22)19(24)20(25)15(2,3)7-6-8-17(20,11-26-19)18(12,23)13(21)10-16/h5,9,13,21,23-25H,1,6-8,10-11H2,2-4H3/t13-,16-,17+,18?,19+,20-/m1/s1
InChI Key FVYIOIBMUVNZMQ-RUPLKUBASA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O6
Molecular Weight 364.40 g/mol
Exact Mass 364.18858861 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.83
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Diaporthein B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9663 96.63%
Caco-2 - 0.5982 59.82%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7760 77.60%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.8977 89.77%
OATP1B3 inhibitior + 0.9068 90.68%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6792 67.92%
BSEP inhibitior - 0.6318 63.18%
P-glycoprotein inhibitior - 0.8345 83.45%
P-glycoprotein substrate - 0.7320 73.20%
CYP3A4 substrate + 0.6361 63.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8471 84.71%
CYP3A4 inhibition - 0.8492 84.92%
CYP2C9 inhibition - 0.7025 70.25%
CYP2C19 inhibition - 0.8160 81.60%
CYP2D6 inhibition - 0.9303 93.03%
CYP1A2 inhibition - 0.7994 79.94%
CYP2C8 inhibition - 0.6899 68.99%
CYP inhibitory promiscuity - 0.9419 94.19%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5589 55.89%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.9656 96.56%
Skin irritation + 0.5436 54.36%
Skin corrosion - 0.9274 92.74%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4639 46.39%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.5715 57.15%
skin sensitisation - 0.8482 84.82%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6084 60.84%
Estrogen receptor binding + 0.5943 59.43%
Androgen receptor binding + 0.7168 71.68%
Thyroid receptor binding + 0.6081 60.81%
Glucocorticoid receptor binding - 0.4632 46.32%
Aromatase binding + 0.7176 71.76%
PPAR gamma - 0.5297 52.97%
Honey bee toxicity - 0.7999 79.99%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9949 99.49%

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 96.60% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.38% 94.45%
CHEMBL2581 P07339 Cathepsin D 93.27% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 92.31% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.93% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.76% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.59% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.14% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.87% 89.00%
CHEMBL4208 P20618 Proteasome component C5 83.24% 90.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.26% 91.07%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.18% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.56% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.41% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 81.17% 94.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139587002
LOTUS LTS0131431
wikiData Q77519123