4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-10-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-3,4,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picen-5-one

Details

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Internal ID c4a22214-2b1b-4d3b-bbf2-a0200bcf2ff5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-10-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-3,4,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picen-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C42H68O13/c1-37(2)14-15-42(20-44)22(16-37)21-8-9-26-39(5)12-11-28(38(3,4)25(39)10-13-40(26,6)41(21,7)17-27(42)45)55-36-34(51)32(49)30(47)24(54-36)19-52-35-33(50)31(48)29(46)23(18-43)53-35/h8,22-26,28-36,43-44,46-51H,9-20H2,1-7H3
InChI Key YDKYBKVODMIZDP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C42H68O13
Molecular Weight 781.00 g/mol
Exact Mass 780.46599222 g/mol
Topological Polar Surface Area (TPSA) 216.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 1.97
H-Bond Acceptor 13
H-Bond Donor 8
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-10-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-3,4,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picen-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7499 74.99%
Caco-2 - 0.8823 88.23%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.8758 87.58%
OATP2B1 inhibitior - 0.8742 87.42%
OATP1B1 inhibitior + 0.7969 79.69%
OATP1B3 inhibitior - 0.5977 59.77%
MATE1 inhibitior - 0.9812 98.12%
OCT2 inhibitior - 0.5776 57.76%
BSEP inhibitior + 0.5886 58.86%
P-glycoprotein inhibitior + 0.7493 74.93%
P-glycoprotein substrate - 0.8250 82.50%
CYP3A4 substrate + 0.7089 70.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8581 85.81%
CYP3A4 inhibition - 0.9589 95.89%
CYP2C9 inhibition - 0.8763 87.63%
CYP2C19 inhibition - 0.9003 90.03%
CYP2D6 inhibition - 0.9427 94.27%
CYP1A2 inhibition - 0.8671 86.71%
CYP2C8 inhibition + 0.5605 56.05%
CYP inhibitory promiscuity - 0.9423 94.23%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6313 63.13%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9132 91.32%
Skin irritation - 0.6520 65.20%
Skin corrosion - 0.9500 95.00%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6652 66.52%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.7670 76.70%
skin sensitisation - 0.8940 89.40%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.7577 75.77%
Acute Oral Toxicity (c) III 0.7822 78.22%
Estrogen receptor binding + 0.7358 73.58%
Androgen receptor binding + 0.7205 72.05%
Thyroid receptor binding - 0.6446 64.46%
Glucocorticoid receptor binding + 0.6451 64.51%
Aromatase binding + 0.6647 66.47%
PPAR gamma + 0.7234 72.34%
Honey bee toxicity - 0.7297 72.97%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6150 61.50%
Fish aquatic toxicity + 0.9603 96.03%

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 98.17% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.64% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.08% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.10% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 88.51% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.97% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.13% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 86.92% 96.61%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.84% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.29% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.05% 93.04%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.24% 94.00%
CHEMBL5255 O00206 Toll-like receptor 4 84.99% 92.50%
CHEMBL221 P23219 Cyclooxygenase-1 84.72% 90.17%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.60% 96.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.27% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.53% 92.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.18% 94.45%
CHEMBL1871 P10275 Androgen Receptor 80.19% 96.43%

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.
Maesa lanceolata

Cross-Links

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PubChem 162970972
LOTUS LTS0159534
wikiData Q105346799