(3S,5R,8S)-5,8-Epoxy-5,8-dihydro-beta,beta-caroten-3-ol

Details

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Internal ID a342180a-f574-4dca-8ce7-4826d1fec6d1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (2S,6S,7aR)-4,4,7a-trimethyl-2-[(2E,4E,6E,8E,10E,12E,14E,16E)-6,11,15-trimethyl-17-(2,6,6-trimethylcyclohexen-1-yl)heptadeca-2,4,6,8,10,12,14,16-octaen-2-yl]-2,5,6,7-tetrahydro-1-benzofuran-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C40H56O2/c1-29(18-13-19-31(3)23-24-35-32(4)22-15-25-38(35,6)7)16-11-12-17-30(2)20-14-21-33(5)36-26-37-39(8,9)27-34(41)28-40(37,10)42-36/h11-14,16-21,23-24,26,34,36,41H,15,22,25,27-28H2,1-10H3/b12-11+,18-13+,20-14+,24-23+,29-16+,30-17+,31-19+,33-21+/t34-,36-,40+/m0/s1
InChI Key DCWLOCNJVDYFMA-TWQKQLNXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C40H56O2
Molecular Weight 568.90 g/mol
Exact Mass 568.42803102 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 11.30
Atomic LogP (AlogP) 10.79
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,5R,8S)-5,8-Epoxy-5,8-dihydro-beta,beta-caroten-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.7892 78.92%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.4134 41.34%
OATP2B1 inhibitior - 0.5703 57.03%
OATP1B1 inhibitior - 0.4221 42.21%
OATP1B3 inhibitior + 0.9730 97.30%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.9964 99.64%
P-glycoprotein inhibitior + 0.8296 82.96%
P-glycoprotein substrate - 0.6285 62.85%
CYP3A4 substrate + 0.6915 69.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7436 74.36%
CYP3A4 inhibition - 0.8615 86.15%
CYP2C9 inhibition - 0.8946 89.46%
CYP2C19 inhibition - 0.7705 77.05%
CYP2D6 inhibition - 0.9303 93.03%
CYP1A2 inhibition - 0.6310 63.10%
CYP2C8 inhibition + 0.5763 57.63%
CYP inhibitory promiscuity - 0.7412 74.12%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4396 43.96%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9181 91.81%
Skin irritation + 0.5168 51.68%
Skin corrosion - 0.9157 91.57%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8701 87.01%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5276 52.76%
skin sensitisation + 0.5142 51.42%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.7155 71.55%
Acute Oral Toxicity (c) III 0.3470 34.70%
Estrogen receptor binding + 0.8280 82.80%
Androgen receptor binding + 0.7687 76.87%
Thyroid receptor binding + 0.7142 71.42%
Glucocorticoid receptor binding + 0.8116 81.16%
Aromatase binding - 0.5683 56.83%
PPAR gamma + 0.7305 73.05%
Honey bee toxicity - 0.7470 74.70%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9015 90.15%

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 97.97% 91.11%
CHEMBL2061 P19793 Retinoid X receptor alpha 92.75% 91.67%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.71% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.13% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.97% 95.56%
CHEMBL2004 P48443 Retinoid X receptor gamma 89.75% 100.00%
CHEMBL1870 P28702 Retinoid X receptor beta 89.50% 95.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.42% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.77% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.71% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.46% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 86.37% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 85.53% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.35% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.03% 94.45%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.72% 91.71%
CHEMBL2581 P07339 Cathepsin D 81.82% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 81.70% 83.82%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.97% 92.62%

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.
Psidium guajava

Cross-Links

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PubChem 15847405
LOTUS LTS0081618
wikiData Q104975955