Hueafuranoid B

Details

Top
Internal ID 1bfd6996-26cf-45e0-9193-cf13b1a9d290
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 6-hydroxy-6-[(2S,5S)-5-[(1E)-4-hydroxy-4-methylhexa-1,5-dienyl]-5-methyloxolan-2-yl]-2-methylhept-2-en-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O4/c1-7-18(4,22)10-8-11-19(5)12-9-17(24-19)20(6,23)14-16(21)13-15(2)3/h7-8,11,13,17,22-23H,1,9-10,12,14H2,2-6H3/b11-8+/t17-,18?,19+,20?/m0/s1
InChI Key HYSXHSFJFJWWOB-FTGFIKAVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H32O4
Molecular Weight 336.50 g/mol
Exact Mass 336.23005950 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Hueafuranoid B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9694 96.94%
Caco-2 + 0.5905 59.05%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5849 58.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8873 88.73%
OATP1B3 inhibitior + 0.9296 92.96%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.6899 68.99%
P-glycoprotein inhibitior - 0.7502 75.02%
P-glycoprotein substrate - 0.8174 81.74%
CYP3A4 substrate + 0.6752 67.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8737 87.37%
CYP3A4 inhibition - 0.7524 75.24%
CYP2C9 inhibition - 0.6927 69.27%
CYP2C19 inhibition - 0.6188 61.88%
CYP2D6 inhibition - 0.9192 91.92%
CYP1A2 inhibition - 0.6659 66.59%
CYP2C8 inhibition - 0.6184 61.84%
CYP inhibitory promiscuity - 0.8335 83.35%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7828 78.28%
Carcinogenicity (trinary) Non-required 0.6190 61.90%
Eye corrosion - 0.9679 96.79%
Eye irritation - 0.9007 90.07%
Skin irritation - 0.5414 54.14%
Skin corrosion - 0.9421 94.21%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5679 56.79%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5649 56.49%
skin sensitisation - 0.6250 62.50%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.5753 57.53%
Acute Oral Toxicity (c) III 0.5371 53.71%
Estrogen receptor binding + 0.6748 67.48%
Androgen receptor binding - 0.6171 61.71%
Thyroid receptor binding + 0.7259 72.59%
Glucocorticoid receptor binding + 0.7035 70.35%
Aromatase binding + 0.5187 51.87%
PPAR gamma + 0.5865 58.65%
Honey bee toxicity - 0.7323 73.23%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9578 95.78%

Targets

Top

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.53% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.37% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.08% 91.11%
CHEMBL218 P21554 Cannabinoid CB1 receptor 90.90% 96.61%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.24% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.85% 91.07%
CHEMBL340 P08684 Cytochrome P450 3A4 86.31% 91.19%
CHEMBL5028 O14672 ADAM10 84.42% 97.50%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.94% 90.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.83% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 82.65% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.53% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.20% 92.62%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.59% 97.28%
CHEMBL2061 P19793 Retinoid X receptor alpha 81.49% 91.67%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.37% 96.47%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.74% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.19% 95.89%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 71530931
LOTUS LTS0230693
wikiData Q105035460