9-Deacetyl Taxinine

Details

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Internal ID 1c8dee37-b446-4875-a295-61d767df8734
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Taxanes and derivatives
IUPAC Name [(1R,2R,3R,5S,8R,9R,10R)-2,10-diacetyloxy-9-hydroxy-8,12,15,15-tetramethyl-4-methylidene-13-oxo-5-tricyclo[9.3.1.03,8]pentadec-11-enyl] (E)-3-phenylprop-2-enoate
SMILES (Canonical) CC1=C2C(C(C3(CCC(C(=C)C3C(C(C2(C)C)CC1=O)OC(=O)C)OC(=O)C=CC4=CC=CC=C4)C)O)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)/C=C/C4=CC=CC=C4)C)O)OC(=O)C
InChI InChI=1S/C33H40O8/c1-18-24(36)17-23-29(39-20(3)34)28-19(2)25(41-26(37)14-13-22-11-9-8-10-12-22)15-16-33(28,7)31(38)30(40-21(4)35)27(18)32(23,5)6/h8-14,23,25,28-31,38H,2,15-17H2,1,3-7H3/b14-13+/t23-,25-,28-,29+,30+,31-,33+/m0/s1
InChI Key CZLWREWIXSHVJD-AYFFSUKUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C33H40O8
Molecular Weight 564.70 g/mol
Exact Mass 564.27231823 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.75
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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CHEMBL434235

2D Structure

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2D Structure of 9-Deacetyl Taxinine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 - 0.8081 80.81%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8520 85.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7995 79.95%
OATP1B3 inhibitior - 0.3856 38.56%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7321 73.21%
BSEP inhibitior + 0.9261 92.61%
P-glycoprotein inhibitior + 0.8466 84.66%
P-glycoprotein substrate - 0.6016 60.16%
CYP3A4 substrate + 0.7055 70.55%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8966 89.66%
CYP3A4 inhibition - 0.5928 59.28%
CYP2C9 inhibition - 0.6655 66.55%
CYP2C19 inhibition - 0.6845 68.45%
CYP2D6 inhibition - 0.8264 82.64%
CYP1A2 inhibition - 0.5624 56.24%
CYP2C8 inhibition + 0.7110 71.10%
CYP inhibitory promiscuity - 0.8303 83.03%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9254 92.54%
Carcinogenicity (trinary) Non-required 0.6233 62.33%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9212 92.12%
Skin irritation - 0.5714 57.14%
Skin corrosion - 0.9299 92.99%
Ames mutagenesis - 0.7128 71.28%
Human Ether-a-go-go-Related Gene inhibition + 0.7071 70.71%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.5176 51.76%
skin sensitisation - 0.6112 61.12%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7388 73.88%
Acute Oral Toxicity (c) III 0.6920 69.20%
Estrogen receptor binding + 0.7229 72.29%
Androgen receptor binding + 0.7322 73.22%
Thyroid receptor binding + 0.6046 60.46%
Glucocorticoid receptor binding + 0.7984 79.84%
Aromatase binding + 0.5832 58.32%
PPAR gamma + 0.7564 75.64%
Honey bee toxicity - 0.6818 68.18%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6200 62.00%
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
CHEMBL4040 P28482 MAP kinase ERK2 98.13% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 97.79% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 97.04% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.42% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.18% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.09% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.19% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.91% 96.09%
CHEMBL5028 O14672 ADAM10 90.49% 97.50%
CHEMBL2581 P07339 Cathepsin D 90.33% 98.95%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 90.03% 94.08%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.54% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 85.94% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.25% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.01% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.45% 95.50%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 83.74% 97.33%
CHEMBL3524 P56524 Histone deacetylase 4 83.54% 92.97%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.61% 93.00%

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 baccata
Taxus cuspidata

Cross-Links

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PubChem 10603013
LOTUS LTS0230287
wikiData Q104972881