[(1R,2R,4R,5R,8R,10S,13R,14R,17R,18S,19S,20S)-2-hydroxy-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-yl] acetate

Details

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Internal ID 6a96492f-ca98-43a8-aece-b8101b5d92b8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [(1R,2R,4R,5R,8R,10S,13R,14R,17R,18S,19S,20S)-2-hydroxy-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-yl] acetate
SMILES (Canonical) CC1CCC23C(CC4(C(C2C1(OC3=O)C)CCC5C4(CCC6C5(CCC(C6(C)C)OC(=O)C)C)C)C)O
SMILES (Isomeric) C[C@H]1CC[C@]23[C@@H](C[C@@]4([C@@H]([C@@H]2[C@]1(OC3=O)C)CC[C@H]5[C@]4(CC[C@@H]6[C@@]5(CC[C@@H](C6(C)C)OC(=O)C)C)C)C)O
InChI InChI=1S/C32H50O5/c1-18-11-16-32-23(34)17-30(7)20(25(32)31(18,8)37-26(32)35)9-10-22-28(5)14-13-24(36-19(2)33)27(3,4)21(28)12-15-29(22,30)6/h18,20-25,34H,9-17H2,1-8H3/t18-,20+,21-,22+,23+,24-,25+,28-,29+,30+,31-,32-/m0/s1
InChI Key LMAQNHCBSLCTIL-YUOOOASKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H50O5
Molecular Weight 514.70 g/mol
Exact Mass 514.36582469 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 7.10
Atomic LogP (AlogP) 6.31
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,2R,4R,5R,8R,10S,13R,14R,17R,18S,19S,20S)-2-hydroxy-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9828 98.28%
Caco-2 - 0.6780 67.80%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7444 74.44%
OATP2B1 inhibitior - 0.7117 71.17%
OATP1B1 inhibitior + 0.8457 84.57%
OATP1B3 inhibitior + 0.8423 84.23%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7571 75.71%
BSEP inhibitior + 0.7270 72.70%
P-glycoprotein inhibitior + 0.5999 59.99%
P-glycoprotein substrate - 0.6697 66.97%
CYP3A4 substrate + 0.7360 73.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8353 83.53%
CYP3A4 inhibition - 0.6749 67.49%
CYP2C9 inhibition - 0.6653 66.53%
CYP2C19 inhibition - 0.7106 71.06%
CYP2D6 inhibition - 0.9686 96.86%
CYP1A2 inhibition - 0.7678 76.78%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.9705 97.05%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6577 65.77%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9141 91.41%
Skin irritation - 0.5208 52.08%
Skin corrosion - 0.8641 86.41%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4120 41.20%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.6592 65.92%
skin sensitisation - 0.8637 86.37%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.6935 69.35%
Acute Oral Toxicity (c) III 0.2913 29.13%
Estrogen receptor binding + 0.6998 69.98%
Androgen receptor binding + 0.7368 73.68%
Thyroid receptor binding + 0.5345 53.45%
Glucocorticoid receptor binding + 0.6645 66.45%
Aromatase binding + 0.6962 69.62%
PPAR gamma + 0.6226 62.26%
Honey bee toxicity - 0.6944 69.44%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5850 58.50%
Fish aquatic toxicity + 0.9868 98.68%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.15% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.15% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.02% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.00% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.43% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.16% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.69% 92.94%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.67% 97.14%
CHEMBL2581 P07339 Cathepsin D 84.67% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 84.50% 91.19%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.60% 96.61%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.39% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.22% 89.00%
CHEMBL1871 P10275 Androgen Receptor 82.00% 96.43%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.37% 97.28%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.24% 96.77%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.04% 93.04%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.04% 93.00%

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.
Pieris japonica

Cross-Links

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PubChem 162862836
LOTUS LTS0026745
wikiData Q105153823