2-[(2R,4aR,8aS)-4a-methyl-8-methylidene-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid

Details

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Internal ID 4a48e819-ff20-4aa6-8e30-183696134206
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name 2-[(2R,4aR,8aS)-4a-methyl-8-methylidene-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid
SMILES (Canonical) CC12CCCC(=C)C1(CC(CC2)C(=C)C(=O)O)OC3C(C(C(C(O3)CO)O)O)O
SMILES (Isomeric) C[C@]12CCCC(=C)[C@]1(C[C@@H](CC2)C(=C)C(=O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O
InChI InChI=1S/C21H32O8/c1-11-5-4-7-20(3)8-6-13(12(2)18(26)27)9-21(11,20)29-19-17(25)16(24)15(23)14(10-22)28-19/h13-17,19,22-25H,1-2,4-10H2,3H3,(H,26,27)/t13-,14-,15-,16+,17-,19+,20-,21+/m1/s1
InChI Key AXCIWKFMHXCHTN-IUUONHNASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O8
Molecular Weight 412.50 g/mol
Exact Mass 412.20971797 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.73
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[(2R,4aR,8aS)-4a-methyl-8-methylidene-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7415 74.15%
Caco-2 - 0.6960 69.60%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7897 78.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8522 85.22%
OATP1B3 inhibitior + 0.8605 86.05%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7096 70.96%
BSEP inhibitior - 0.8831 88.31%
P-glycoprotein inhibitior - 0.7750 77.50%
P-glycoprotein substrate - 0.8551 85.51%
CYP3A4 substrate + 0.6279 62.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8880 88.80%
CYP3A4 inhibition - 0.8897 88.97%
CYP2C9 inhibition - 0.8672 86.72%
CYP2C19 inhibition - 0.8112 81.12%
CYP2D6 inhibition - 0.9300 93.00%
CYP1A2 inhibition - 0.7210 72.10%
CYP2C8 inhibition - 0.5592 55.92%
CYP inhibitory promiscuity - 0.8889 88.89%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7291 72.91%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9362 93.62%
Skin irritation - 0.6135 61.35%
Skin corrosion - 0.9473 94.73%
Ames mutagenesis - 0.5637 56.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6524 65.24%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.7171 71.71%
skin sensitisation - 0.8763 87.63%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6155 61.55%
Acute Oral Toxicity (c) III 0.6225 62.25%
Estrogen receptor binding + 0.5998 59.98%
Androgen receptor binding + 0.6057 60.57%
Thyroid receptor binding + 0.5485 54.85%
Glucocorticoid receptor binding - 0.4849 48.49%
Aromatase binding + 0.6731 67.31%
PPAR gamma + 0.6100 61.00%
Honey bee toxicity - 0.8273 82.73%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9765 97.65%

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 98.13% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.94% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.74% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.34% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.67% 97.25%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.98% 91.24%
CHEMBL3714130 P46095 G-protein coupled receptor 6 86.78% 97.36%
CHEMBL221 P23219 Cyclooxygenase-1 84.92% 90.17%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.70% 95.50%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.64% 96.61%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.51% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.45% 95.56%
CHEMBL237 P41145 Kappa opioid receptor 81.72% 98.10%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 81.57% 96.38%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.17% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.02% 89.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.84% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.66% 95.50%
CHEMBL2581 P07339 Cathepsin D 80.32% 98.95%

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.
Laggera alata
Sesamum alatum

Cross-Links

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PubChem 11015134
LOTUS LTS0222108
wikiData Q104920432