[(1R,2R,3R,5S,8R,9R,10R)-2,9,10-triacetyloxy-8,12,15,15-tetramethyl-4-methylidene-13-oxo-5-tricyclo[9.3.1.03,8]pentadec-11-enyl] benzoate

Details

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Internal ID c4c55cf9-4752-4820-b0c6-1efccd87e926
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Taxanes and derivatives
IUPAC Name [(1R,2R,3R,5S,8R,9R,10R)-2,9,10-triacetyloxy-8,12,15,15-tetramethyl-4-methylidene-13-oxo-5-tricyclo[9.3.1.03,8]pentadec-11-enyl] benzoate
SMILES (Canonical) CC1=C2C(C(C3(CCC(C(=C)C3C(C(C2(C)C)CC1=O)OC(=O)C)OC(=O)C4=CC=CC=C4)C)OC(=O)C)OC(=O)C
SMILES (Isomeric) CC1=C2[C@H]([C@@H]([C@@]3(CC[C@@H](C(=C)[C@H]3[C@@H]([C@@H](C2(C)C)CC1=O)OC(=O)C)OC(=O)C4=CC=CC=C4)C)OC(=O)C)OC(=O)C
InChI InChI=1S/C33H40O9/c1-17-24(37)16-23-28(39-19(3)34)27-18(2)25(42-31(38)22-12-10-9-11-13-22)14-15-33(27,8)30(41-21(5)36)29(40-20(4)35)26(17)32(23,6)7/h9-13,23,25,27-30H,2,14-16H2,1,3-8H3/t23-,25-,27-,28+,29+,30-,33+/m0/s1
InChI Key KCVBKOGPGLTLNX-KQDCEKGYSA-N
Popularity 2 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) 122.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.92
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,2R,3R,5S,8R,9R,10R)-2,9,10-triacetyloxy-8,12,15,15-tetramethyl-4-methylidene-13-oxo-5-tricyclo[9.3.1.03,8]pentadec-11-enyl] benzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 - 0.7454 74.54%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7914 79.14%
OATP2B1 inhibitior - 0.7181 71.81%
OATP1B1 inhibitior + 0.7979 79.79%
OATP1B3 inhibitior + 0.8138 81.38%
MATE1 inhibitior + 0.6600 66.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9483 94.83%
P-glycoprotein inhibitior + 0.9055 90.55%
P-glycoprotein substrate - 0.6453 64.53%
CYP3A4 substrate + 0.6953 69.53%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8922 89.22%
CYP3A4 inhibition + 0.6569 65.69%
CYP2C9 inhibition - 0.6878 68.78%
CYP2C19 inhibition - 0.6062 60.62%
CYP2D6 inhibition - 0.7995 79.95%
CYP1A2 inhibition - 0.6537 65.37%
CYP2C8 inhibition + 0.7159 71.59%
CYP inhibitory promiscuity - 0.7427 74.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8772 87.72%
Carcinogenicity (trinary) Non-required 0.5647 56.47%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.8735 87.35%
Skin irritation - 0.6434 64.34%
Skin corrosion - 0.9537 95.37%
Ames mutagenesis - 0.6828 68.28%
Human Ether-a-go-go-Related Gene inhibition - 0.4429 44.29%
Micronuclear - 0.6500 65.00%
Hepatotoxicity - 0.5051 50.51%
skin sensitisation + 0.4774 47.74%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.5639 56.39%
Acute Oral Toxicity (c) III 0.6186 61.86%
Estrogen receptor binding + 0.7899 78.99%
Androgen receptor binding + 0.6990 69.90%
Thyroid receptor binding + 0.6307 63.07%
Glucocorticoid receptor binding + 0.7903 79.03%
Aromatase binding + 0.5478 54.78%
PPAR gamma + 0.7730 77.30%
Honey bee toxicity - 0.7047 70.47%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
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
CHEMBL221 P23219 Cyclooxygenase-1 96.99% 90.17%
CHEMBL2581 P07339 Cathepsin D 94.24% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.80% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.06% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.03% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.84% 96.09%
CHEMBL5028 O14672 ADAM10 88.87% 97.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.30% 94.62%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.20% 93.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.13% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.48% 95.50%
CHEMBL340 P08684 Cytochrome P450 3A4 84.01% 91.19%
CHEMBL4040 P28482 MAP kinase ERK2 83.62% 83.82%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.29% 81.11%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 82.91% 83.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.86% 82.69%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.34% 93.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.69% 97.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.10% 100.00%

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.
Taxus cuspidata

Cross-Links

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PubChem 15378568
LOTUS LTS0260970
wikiData Q105138966