Trans-dihydrowaol A

Details

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Internal ID d6e046fd-55d4-4789-b004-579e860cfad8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > C-glycosyl compounds
IUPAC Name (2R,3R,4aR,7S,7aR)-3-hydroxy-2,7-bis[(E)-prop-1-enyl]-2,3,4,4a,7,7a-hexahydrofuro[3,4-b]pyran-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H18O4/c1-3-5-10-9(14)7-8-12(16-10)11(6-4-2)17-13(8)15/h3-6,8-12,14H,7H2,1-2H3/b5-3+,6-4+/t8-,9-,10-,11+,12-/m1/s1
InChI Key HYIOVPCFUNFYCR-AMEDQPCTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O4
Molecular Weight 238.28 g/mol
Exact Mass 238.12050905 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Trans-dihydrowaol A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9766 97.66%
Caco-2 - 0.7482 74.82%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6440 64.40%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.8943 89.43%
OATP1B3 inhibitior + 0.9194 91.94%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8850 88.50%
P-glycoprotein inhibitior - 0.9536 95.36%
P-glycoprotein substrate - 0.8859 88.59%
CYP3A4 substrate - 0.5156 51.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8587 85.87%
CYP3A4 inhibition - 0.8322 83.22%
CYP2C9 inhibition - 0.9898 98.98%
CYP2C19 inhibition - 0.9563 95.63%
CYP2D6 inhibition - 0.9376 93.76%
CYP1A2 inhibition - 0.9182 91.82%
CYP2C8 inhibition - 0.9705 97.05%
CYP inhibitory promiscuity - 0.9673 96.73%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4343 43.43%
Eye corrosion - 0.9285 92.85%
Eye irritation - 0.8824 88.24%
Skin irritation - 0.5358 53.58%
Skin corrosion - 0.8793 87.93%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5921 59.21%
Micronuclear + 0.5659 56.59%
Hepatotoxicity + 0.8141 81.41%
skin sensitisation - 0.7860 78.60%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.4850 48.50%
Acute Oral Toxicity (c) III 0.3791 37.91%
Estrogen receptor binding - 0.6466 64.66%
Androgen receptor binding - 0.6390 63.90%
Thyroid receptor binding - 0.6290 62.90%
Glucocorticoid receptor binding - 0.5369 53.69%
Aromatase binding - 0.8509 85.09%
PPAR gamma - 0.7506 75.06%
Honey bee toxicity - 0.8587 85.87%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.6210 62.10%

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 90.95% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.60% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.14% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.72% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.71% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.36% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.94% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.13% 100.00%

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 71816805
LOTUS LTS0168472
wikiData Q105035332