[(1E,3S,4R,6S,9R,11S,12S,14S)-3,12-diacetyloxy-9,14-dihydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] (E)-3-phenylprop-2-enoate

Details

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Internal ID 35065ae3-8495-4710-b518-af0387f331e6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Taxanes and derivatives
IUPAC Name [(1E,3S,4R,6S,9R,11S,12S,14S)-3,12-diacetyloxy-9,14-dihydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] (E)-3-phenylprop-2-enoate
SMILES (Canonical) CC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C=CC4=CC=CC=C4)OC(=O)C)C(CC3OC(=O)C)O)C)O
SMILES (Isomeric) CC1=C2[C@H](C(=O)[C@]3(C/C(=C\[C@@H]([C@@H](C2(C)C)C[C@@H]1OC(=O)/C=C/C4=CC=CC=C4)OC(=O)C)/[C@H](C[C@@H]3OC(=O)C)O)C)O
InChI InChI=1S/C33H40O9/c1-18-25(42-28(37)13-12-21-10-8-7-9-11-21)15-23-26(40-19(2)34)14-22-17-33(6,27(16-24(22)36)41-20(3)35)31(39)30(38)29(18)32(23,4)5/h7-14,23-27,30,36,38H,15-17H2,1-6H3/b13-12+,22-14+/t23-,24-,25-,26-,27-,30+,33-/m0/s1
InChI Key YAWRAQDREAECPJ-IHNXBZDVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C33H40O9
Molecular Weight 580.70 g/mol
Exact Mass 580.26723285 g/mol
Topological Polar Surface Area (TPSA) 136.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.87
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1E,3S,4R,6S,9R,11S,12S,14S)-3,12-diacetyloxy-9,14-dihydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] (E)-3-phenylprop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 - 0.7761 77.61%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7922 79.22%
OATP2B1 inhibitior - 0.7156 71.56%
OATP1B1 inhibitior + 0.8112 81.12%
OATP1B3 inhibitior - 0.2508 25.08%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.9864 98.64%
P-glycoprotein inhibitior + 0.8739 87.39%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6930 69.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8852 88.52%
CYP3A4 inhibition - 0.5488 54.88%
CYP2C9 inhibition - 0.7674 76.74%
CYP2C19 inhibition - 0.7753 77.53%
CYP2D6 inhibition - 0.9143 91.43%
CYP1A2 inhibition - 0.7290 72.90%
CYP2C8 inhibition + 0.7740 77.40%
CYP inhibitory promiscuity - 0.8734 87.34%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9443 94.43%
Carcinogenicity (trinary) Non-required 0.5639 56.39%
Eye corrosion - 0.9932 99.32%
Eye irritation - 0.9281 92.81%
Skin irritation - 0.5630 56.30%
Skin corrosion - 0.9508 95.08%
Ames mutagenesis + 0.5246 52.46%
Human Ether-a-go-go-Related Gene inhibition - 0.4418 44.18%
Micronuclear - 0.6100 61.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.6606 66.06%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.5676 56.76%
Acute Oral Toxicity (c) I 0.4428 44.28%
Estrogen receptor binding + 0.8453 84.53%
Androgen receptor binding + 0.6834 68.34%
Thyroid receptor binding + 0.6546 65.46%
Glucocorticoid receptor binding + 0.8817 88.17%
Aromatase binding + 0.6209 62.09%
PPAR gamma + 0.7740 77.40%
Honey bee toxicity - 0.6480 64.80%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 1.0000 100.00%

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 97.18% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.08% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.05% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 94.32% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.58% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.57% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 91.95% 90.17%
CHEMBL4040 P28482 MAP kinase ERK2 91.29% 83.82%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.15% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.51% 85.14%
CHEMBL5028 O14672 ADAM10 87.96% 97.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.89% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.71% 99.23%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.73% 93.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 85.46% 94.08%
CHEMBL2581 P07339 Cathepsin D 85.27% 98.95%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.81% 94.23%
CHEMBL340 P08684 Cytochrome P450 3A4 80.60% 91.19%

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.
Taxus baccata

Cross-Links

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PubChem 163191304
LOTUS LTS0003521
wikiData Q105345644