(1S,4S,7S,9S,10R,13R,14R)-7,14-dihydroxy-5,5,9-trimethyl-14-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecan-6-one

Details

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Internal ID 01fd60e3-d8c1-48e8-a232-9238804f2cdf
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Diterpene glycosides
IUPAC Name (1S,4S,7S,9S,10R,13R,14R)-7,14-dihydroxy-5,5,9-trimethyl-14-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecan-6-one
SMILES (Canonical) CC1(C2CCC34CC(CCC3C2(CC(C1=O)O)C)C(C4)(COC5C(C(C(C(O5)CO)O)O)O)O)C
SMILES (Isomeric) C[C@@]12C[C@@H](C(=O)C([C@H]1CC[C@]34[C@H]2CC[C@H](C3)[C@](C4)(CO[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)O)(C)C)O
InChI InChI=1S/C26H42O9/c1-23(2)16-6-7-25-8-13(4-5-17(25)24(16,3)9-14(28)21(23)32)26(33,11-25)12-34-22-20(31)19(30)18(29)15(10-27)35-22/h13-20,22,27-31,33H,4-12H2,1-3H3/t13-,14+,15-,16-,17+,18-,19+,20-,22-,24-,25+,26+/m1/s1
InChI Key ACDWTWHJUYGFKM-MEJKCINQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H42O9
Molecular Weight 498.60 g/mol
Exact Mass 498.28288291 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.12
H-Bond Acceptor 9
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4S,7S,9S,10R,13R,14R)-7,14-dihydroxy-5,5,9-trimethyl-14-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecan-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6519 65.19%
Caco-2 - 0.8384 83.84%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7117 71.17%
OATP2B1 inhibitior - 0.7176 71.76%
OATP1B1 inhibitior + 0.8912 89.12%
OATP1B3 inhibitior + 0.9078 90.78%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9224 92.24%
P-glycoprotein inhibitior - 0.5496 54.96%
P-glycoprotein substrate - 0.7225 72.25%
CYP3A4 substrate + 0.6802 68.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8544 85.44%
CYP3A4 inhibition - 0.9149 91.49%
CYP2C9 inhibition - 0.8096 80.96%
CYP2C19 inhibition - 0.8189 81.89%
CYP2D6 inhibition - 0.9582 95.82%
CYP1A2 inhibition - 0.8663 86.63%
CYP2C8 inhibition - 0.5667 56.67%
CYP inhibitory promiscuity - 0.9717 97.17%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7346 73.46%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9397 93.97%
Skin irritation - 0.6852 68.52%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6477 64.77%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.8088 80.88%
skin sensitisation - 0.9224 92.24%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.4940 49.40%
Acute Oral Toxicity (c) I 0.4278 42.78%
Estrogen receptor binding + 0.6953 69.53%
Androgen receptor binding + 0.6693 66.93%
Thyroid receptor binding - 0.5263 52.63%
Glucocorticoid receptor binding + 0.6684 66.84%
Aromatase binding + 0.6862 68.62%
PPAR gamma + 0.5437 54.37%
Honey bee toxicity - 0.7955 79.55%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6450 64.50%
Fish aquatic toxicity + 0.8735 87.35%

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 97.75% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.96% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.85% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.84% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.11% 98.95%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.16% 96.61%
CHEMBL1937 Q92769 Histone deacetylase 2 87.04% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.57% 94.45%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 86.57% 97.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.31% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.34% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.95% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.42% 96.77%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.19% 95.50%
CHEMBL5255 O00206 Toll-like receptor 4 83.18% 92.50%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.57% 96.21%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.29% 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.
Relhania calycina

Cross-Links

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PubChem 162966287
LOTUS LTS0179168
wikiData Q104909033