(4aR,8R,8aS)-8-[[(1R,2R,4aS,7S,8aS)-2,7-dihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-8a-(5,7-dihydroxy-4-oxochromen-2-yl)-3-methoxy-7-methyl-5,8-dihydro-4aH-naphthalene-1,4-dione

Details

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Internal ID bdd89db7-5c52-4a5d-9d0f-ebe8ef9d72a6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aR,8R,8aS)-8-[[(1R,2R,4aS,7S,8aS)-2,7-dihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-8a-(5,7-dihydroxy-4-oxochromen-2-yl)-3-methoxy-7-methyl-5,8-dihydro-4aH-naphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H44O9/c1-18-7-8-21-32(42)26(44-6)15-29(41)36(21,30-14-24(40)31-23(39)11-19(37)12-25(31)45-30)22(18)13-28-34(4)17-20(38)16-33(2,3)27(34)9-10-35(28,5)43/h7,11-12,14-15,20-22,27-28,37-39,43H,8-10,13,16-17H2,1-6H3/t20-,21-,22+,27-,28+,34-,35+,36-/m0/s1
InChI Key XTJPOXSSNPWQEZ-YJJSCDARSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H44O9
Molecular Weight 620.70 g/mol
Exact Mass 620.29853298 g/mol
Topological Polar Surface Area (TPSA) 151.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 5.06
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4aR,8R,8aS)-8-[[(1R,2R,4aS,7S,8aS)-2,7-dihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-8a-(5,7-dihydroxy-4-oxochromen-2-yl)-3-methoxy-7-methyl-5,8-dihydro-4aH-naphthalene-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9739 97.39%
Caco-2 - 0.8199 81.99%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6959 69.59%
OATP2B1 inhibitior - 0.5780 57.80%
OATP1B1 inhibitior + 0.8393 83.93%
OATP1B3 inhibitior + 0.9004 90.04%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8564 85.64%
BSEP inhibitior + 0.9634 96.34%
P-glycoprotein inhibitior + 0.7241 72.41%
P-glycoprotein substrate + 0.6741 67.41%
CYP3A4 substrate + 0.7287 72.87%
CYP2C9 substrate - 0.5915 59.15%
CYP2D6 substrate - 0.8626 86.26%
CYP3A4 inhibition + 0.6059 60.59%
CYP2C9 inhibition - 0.6673 66.73%
CYP2C19 inhibition - 0.5933 59.33%
CYP2D6 inhibition - 0.8795 87.95%
CYP1A2 inhibition - 0.6382 63.82%
CYP2C8 inhibition + 0.7851 78.51%
CYP inhibitory promiscuity - 0.7349 73.49%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7151 71.51%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9187 91.87%
Skin irritation - 0.7171 71.71%
Skin corrosion - 0.9405 94.05%
Ames mutagenesis - 0.5470 54.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4572 45.72%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.5758 57.58%
skin sensitisation - 0.8482 84.82%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7422 74.22%
Acute Oral Toxicity (c) I 0.4788 47.88%
Estrogen receptor binding + 0.8482 84.82%
Androgen receptor binding + 0.7543 75.43%
Thyroid receptor binding + 0.5723 57.23%
Glucocorticoid receptor binding + 0.8724 87.24%
Aromatase binding + 0.7462 74.62%
PPAR gamma + 0.7511 75.11%
Honey bee toxicity - 0.6677 66.77%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9936 99.36%

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 99.64% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.53% 93.99%
CHEMBL1937 Q92769 Histone deacetylase 2 94.22% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.20% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.90% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.38% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.92% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 92.27% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.48% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.00% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.50% 95.89%
CHEMBL3194 P02766 Transthyretin 89.00% 90.71%
CHEMBL2581 P07339 Cathepsin D 88.99% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.29% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.17% 96.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.69% 97.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.97% 92.62%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.27% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.19% 96.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.43% 91.07%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.43% 90.71%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.11% 97.28%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.77% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.16% 99.17%

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.
Dichrostachys cinerea

Cross-Links

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PubChem 44557153
LOTUS LTS0167262
wikiData Q105341602