[2,8,9,16-Tetraacetyloxy-5-hydroxy-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-11-yl] acetate

Details

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Internal ID bd309c0a-520f-46c7-bf11-dbfcb2d3aa35
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Taxanes and derivatives
IUPAC Name [2,8,9,16-tetraacetyloxy-5-hydroxy-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-11-yl] acetate
SMILES (Canonical) CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C
SMILES (Isomeric) CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C
InChI InChI=1S/C30H42O13/c1-13-19(36)11-29(27(7,8)37)22(13)23(40-15(3)32)25(41-16(4)33)28(9)20(39-14(2)31)10-21-30(12-38-21,43-18(6)35)24(28)26(29)42-17(5)34/h19-21,23-26,36-37H,10-12H2,1-9H3
InChI Key TZFNSITZSZGMKW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H42O13
Molecular Weight 610.60 g/mol
Exact Mass 610.26254139 g/mol
Topological Polar Surface Area (TPSA) 181.00 Ų
XlogP -0.30
Atomic LogP (AlogP) 1.29
H-Bond Acceptor 13
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [2,8,9,16-Tetraacetyloxy-5-hydroxy-3-(2-hydroxypropan-2-yl)-6,10-dimethyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-11-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 + 0.9860 98.60%
Caco-2 - 0.7258 72.58%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7809 78.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8856 88.56%
OATP1B3 inhibitior + 0.9482 94.82%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7634 76.34%
P-glycoprotein inhibitior + 0.7435 74.35%
P-glycoprotein substrate + 0.5827 58.27%
CYP3A4 substrate + 0.6883 68.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8607 86.07%
CYP3A4 inhibition - 0.8724 87.24%
CYP2C9 inhibition - 0.7479 74.79%
CYP2C19 inhibition - 0.8597 85.97%
CYP2D6 inhibition - 0.9307 93.07%
CYP1A2 inhibition - 0.7817 78.17%
CYP2C8 inhibition + 0.6803 68.03%
CYP inhibitory promiscuity - 0.9504 95.04%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5037 50.37%
Eye corrosion - 0.9822 98.22%
Eye irritation - 0.8720 87.20%
Skin irritation - 0.6331 63.31%
Skin corrosion - 0.9222 92.22%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5371 53.71%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.7758 77.58%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.7218 72.18%
Acute Oral Toxicity (c) III 0.4708 47.08%
Estrogen receptor binding + 0.8184 81.84%
Androgen receptor binding + 0.7062 70.62%
Thyroid receptor binding + 0.5289 52.89%
Glucocorticoid receptor binding + 0.7293 72.93%
Aromatase binding + 0.7012 70.12%
PPAR gamma + 0.7252 72.52%
Honey bee toxicity - 0.5984 59.84%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5537 55.37%
Fish aquatic toxicity + 0.9683 96.83%

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 97.04% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.99% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.76% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.95% 97.25%
CHEMBL2581 P07339 Cathepsin D 89.32% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.34% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.41% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.96% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 85.77% 91.19%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.24% 89.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.70% 81.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.81% 95.56%
CHEMBL5028 O14672 ADAM10 83.57% 97.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.25% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.15% 92.94%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.53% 95.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.54% 94.33%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.45% 97.28%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.30% 96.77%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.04% 96.95%

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.
Hydrastis canadensis
Taxus canadensis
Taxus cuspidata

Cross-Links

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PubChem 73192583
LOTUS LTS0270773
wikiData Q104956941