Oleana-12-ene-3beta,16beta-diol 3-hexadecanoate

Details

Top
Internal ID 0187968b-bbdf-4936-bd20-b771ae8e94ed
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [(3S,4aR,6aR,6bS,8S,8aS,12aS,14aR,14bR)-8-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] hexadecanoate
SMILES (Canonical) CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CC(C5(C4CC(CC5)(C)C)C)O)C)C)C
SMILES (Isomeric) CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@]2([C@H](C1(C)C)CC[C@@]3([C@@H]2CC=C4[C@]3(C[C@@H]([C@@]5([C@H]4CC(CC5)(C)C)C)O)C)C)C
InChI InChI=1S/C46H80O3/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-40(48)49-39-27-28-44(7)36(42(39,4)5)26-29-45(8)37(44)25-24-34-35-32-41(2,3)30-31-43(35,6)38(47)33-46(34,45)9/h24,35-39,47H,10-23,25-33H2,1-9H3/t35-,36-,37+,38-,39-,43-,44-,45+,46+/m0/s1
InChI Key BPAWXSVOAOLSRP-MUYGVQPCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C46H80O3
Molecular Weight 681.10 g/mol
Exact Mass 680.61074641 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 15.50
Atomic LogP (AlogP) 13.17
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 15

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Oleana-12-ene-3beta,16beta-diol 3-hexadecanoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.7971 79.71%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8193 81.93%
OATP2B1 inhibitior - 0.5669 56.69%
OATP1B1 inhibitior + 0.7622 76.22%
OATP1B3 inhibitior + 0.9820 98.20%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.9456 94.56%
P-glycoprotein inhibitior + 0.7169 71.69%
P-glycoprotein substrate - 0.6359 63.59%
CYP3A4 substrate + 0.7108 71.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8465 84.65%
CYP3A4 inhibition - 0.6777 67.77%
CYP2C9 inhibition - 0.7740 77.40%
CYP2C19 inhibition - 0.6841 68.41%
CYP2D6 inhibition - 0.9234 92.34%
CYP1A2 inhibition - 0.9362 93.62%
CYP2C8 inhibition + 0.6217 62.17%
CYP inhibitory promiscuity - 0.7071 70.71%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9843 98.43%
Carcinogenicity (trinary) Non-required 0.6110 61.10%
Eye corrosion - 0.9938 99.38%
Eye irritation - 0.8962 89.62%
Skin irritation + 0.5617 56.17%
Skin corrosion - 0.9658 96.58%
Ames mutagenesis - 0.8354 83.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6415 64.15%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.8444 84.44%
skin sensitisation - 0.5569 55.69%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8818 88.18%
Acute Oral Toxicity (c) III 0.7508 75.08%
Estrogen receptor binding + 0.6873 68.73%
Androgen receptor binding + 0.6803 68.03%
Thyroid receptor binding - 0.5138 51.38%
Glucocorticoid receptor binding + 0.6559 65.59%
Aromatase binding + 0.6271 62.71%
PPAR gamma + 0.6084 60.84%
Honey bee toxicity - 0.8658 86.58%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.8573 85.73%
Fish aquatic toxicity + 0.9975 99.75%

Targets

Top

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 98.80% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.83% 97.25%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 96.64% 95.17%
CHEMBL221 P23219 Cyclooxygenase-1 95.90% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.47% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.62% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.14% 99.17%
CHEMBL2581 P07339 Cathepsin D 93.07% 98.95%
CHEMBL5255 O00206 Toll-like receptor 4 92.70% 92.50%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.67% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.88% 97.09%
CHEMBL3180 O00748 Carboxylesterase 2 88.75% 90.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 88.05% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.59% 95.89%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.18% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.66% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.41% 100.00%
CHEMBL299 P17252 Protein kinase C alpha 84.84% 98.03%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.54% 92.86%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.51% 92.62%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.23% 94.33%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 82.12% 85.94%
CHEMBL1871 P10275 Androgen Receptor 81.99% 96.43%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 81.46% 90.24%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.26% 97.29%
CHEMBL2996 Q05655 Protein kinase C delta 80.23% 97.79%

Plants that contains it

Top
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.
Achillea alexandri-regis
Arnica lonchophylla
Sinacalia tangutica

Cross-Links

Top
PubChem 11115096
LOTUS LTS0048862
wikiData Q104941311