phi-Taraxasteryl acetate

Details

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Internal ID caf53e51-ffb2-41fd-8014-2ef4315c292b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [(3S,4aR,6aR,6aR,6bR,8aS,11R,12R,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,11,12,12a,13,14,14a-tetradecahydro-1H-picen-3-yl] acetate
SMILES (Canonical) CC1C=CC2(CCC3(C(C2C1C)CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C)C
SMILES (Isomeric) C[C@@H]1C=C[C@@]2(CC[C@@]3([C@@H]([C@H]2[C@@H]1C)CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OC(=O)C)C)C)C)C
InChI InChI=1S/C32H52O2/c1-20-12-15-29(6)18-19-31(8)23(27(29)21(20)2)10-11-25-30(7)16-14-26(34-22(3)33)28(4,5)24(30)13-17-32(25,31)9/h12,15,20-21,23-27H,10-11,13-14,16-19H2,1-9H3/t20-,21-,23-,24+,25-,26+,27-,29-,30+,31-,32-/m1/s1
InChI Key RIDJSNUZLSTKKB-DWTGHIQGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H52O2
Molecular Weight 468.80 g/mol
Exact Mass 468.396730897 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 10.00
Atomic LogP (AlogP) 8.45
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of phi-Taraxasteryl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.6256 62.56%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5979 59.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8371 83.71%
OATP1B3 inhibitior + 0.9663 96.63%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.8463 84.63%
P-glycoprotein inhibitior + 0.6431 64.31%
P-glycoprotein substrate - 0.7611 76.11%
CYP3A4 substrate + 0.7266 72.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8683 86.83%
CYP3A4 inhibition - 0.8532 85.32%
CYP2C9 inhibition - 0.9078 90.78%
CYP2C19 inhibition + 0.6854 68.54%
CYP2D6 inhibition - 0.9626 96.26%
CYP1A2 inhibition - 0.8654 86.54%
CYP2C8 inhibition + 0.5230 52.30%
CYP inhibitory promiscuity - 0.9209 92.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9043 90.43%
Carcinogenicity (trinary) Non-required 0.5360 53.60%
Eye corrosion - 0.9653 96.53%
Eye irritation - 0.9356 93.56%
Skin irritation + 0.5450 54.50%
Skin corrosion - 0.9853 98.53%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6917 69.17%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.7823 78.23%
skin sensitisation + 0.7321 73.21%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.7465 74.65%
Acute Oral Toxicity (c) III 0.8582 85.82%
Estrogen receptor binding + 0.8275 82.75%
Androgen receptor binding + 0.7338 73.38%
Thyroid receptor binding + 0.5982 59.82%
Glucocorticoid receptor binding + 0.7424 74.24%
Aromatase binding + 0.7684 76.84%
PPAR gamma + 0.6477 64.77%
Honey bee toxicity - 0.5956 59.56%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5545 55.45%
Fish aquatic toxicity + 0.9945 99.45%

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 97.77% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.44% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.00% 82.69%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.61% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.95% 92.94%
CHEMBL340 P08684 Cytochrome P450 3A4 86.84% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.39% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.78% 94.75%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.73% 100.00%
CHEMBL2581 P07339 Cathepsin D 83.46% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.03% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.90% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.59% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.38% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.32% 91.11%

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.
Taraxacum coreanum
Taraxacum mongolicum
Taraxacum officinale
Taraxacum platycarpum
Taraxacum sinicum

Cross-Links

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PubChem 101553159
NPASS NPC214134