(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

Details

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Internal ID 72210606-4bf7-40db-bbfe-4663dc23a1d8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(CC7)(C)C)C(=O)O)O)C)C)C)O)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@H](CO[C@H]2O[C@H]3CC[C@]4([C@H](C3(C)C)CC[C@@]5([C@@H]4CC=C6[C@]5(C[C@H]([C@@]7([C@H]6CC(CC7)(C)C)C(=O)O)O)C)C)C)O)O)O)O)O
InChI InChI=1S/C41H66O12/c1-20-28(44)30(46)31(47)33(51-20)53-32-29(45)23(42)19-50-34(32)52-27-12-13-38(6)24(37(27,4)5)11-14-39(7)25(38)10-9-21-22-17-36(2,3)15-16-41(22,35(48)49)26(43)18-40(21,39)8/h9,20,22-34,42-47H,10-19H2,1-8H3,(H,48,49)/t20-,22-,23-,24-,25+,26+,27-,28-,29-,30+,31+,32+,33-,34-,38-,39+,40+,41+/m0/s1
InChI Key WQVNDHHTUJYLTJ-XDNDNJDCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C41H66O12
Molecular Weight 751.00 g/mol
Exact Mass 750.45542754 g/mol
Topological Polar Surface Area (TPSA) 196.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.52
H-Bond Acceptor 11
H-Bond Donor 7
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8956 89.56%
Caco-2 - 0.8777 87.77%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8672 86.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7132 71.32%
OATP1B3 inhibitior - 0.2786 27.86%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6526 65.26%
BSEP inhibitior - 0.5586 55.86%
P-glycoprotein inhibitior + 0.7706 77.06%
P-glycoprotein substrate - 0.6115 61.15%
CYP3A4 substrate + 0.7234 72.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8798 87.98%
CYP3A4 inhibition - 0.9290 92.90%
CYP2C9 inhibition - 0.8742 87.42%
CYP2C19 inhibition - 0.9193 91.93%
CYP2D6 inhibition - 0.9330 93.30%
CYP1A2 inhibition - 0.8587 85.87%
CYP2C8 inhibition + 0.6460 64.60%
CYP inhibitory promiscuity - 0.9661 96.61%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6143 61.43%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.9149 91.49%
Skin irritation - 0.5408 54.08%
Skin corrosion - 0.9417 94.17%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6578 65.78%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.8069 80.69%
skin sensitisation - 0.8585 85.85%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.9031 90.31%
Acute Oral Toxicity (c) III 0.6425 64.25%
Estrogen receptor binding + 0.7064 70.64%
Androgen receptor binding + 0.7101 71.01%
Thyroid receptor binding - 0.5954 59.54%
Glucocorticoid receptor binding + 0.6464 64.64%
Aromatase binding + 0.6683 66.83%
PPAR gamma + 0.7172 71.72%
Honey bee toxicity - 0.7191 71.91%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5095 50.95%
Fish aquatic toxicity + 0.9724 97.24%

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 94.99% 91.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 93.97% 97.36%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.37% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.92% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.99% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.48% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.40% 96.77%
CHEMBL5028 O14672 ADAM10 85.58% 97.50%
CHEMBL2179 P04062 Beta-glucocerebrosidase 85.38% 85.31%
CHEMBL221 P23219 Cyclooxygenase-1 84.91% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.34% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.92% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 80.96% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.75% 95.89%

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.
Hedera canariensis
Hedera caucasigena
Hedera helix

Cross-Links

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PubChem 21630161
LOTUS LTS0275053
wikiData Q105311015