Taxinine NN-4

Details

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Internal ID 7b060dd9-9fe5-4495-a08b-c405620fcd62
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tetracarboxylic acids and derivatives
IUPAC Name [(1R,2S,3R,4R,7S,9R,10R,11R,14S)-2,3,10-triacetyloxy-4,14,16,16-tetramethyl-8-methylidene-13-oxo-15-oxatetracyclo[9.4.1.01,14.04,9]hexadecan-7-yl] (E)-3-phenylprop-2-enoate
SMILES (Canonical) CC(=O)OC1C2CC(=O)C3(C(C2(C)C)(O3)C(C(C4(C1C(=C)C(CC4)OC(=O)C=CC5=CC=CC=C5)C)OC(=O)C)OC(=O)C)C
SMILES (Isomeric) CC(=O)O[C@@H]1[C@@H]2CC(=O)[C@@]3([C@](C2(C)C)(O3)[C@H]([C@@H]([C@]4([C@H]1C(=C)[C@H](CC4)OC(=O)/C=C/C5=CC=CC=C5)C)OC(=O)C)OC(=O)C)C
InChI InChI=1S/C35H42O10/c1-19-25(44-27(40)15-14-23-12-10-9-11-13-23)16-17-33(7)28(19)29(41-20(2)36)24-18-26(39)34(8)35(45-34,32(24,5)6)31(43-22(4)38)30(33)42-21(3)37/h9-15,24-25,28-31H,1,16-18H2,2-8H3/b15-14+/t24-,25-,28-,29+,30-,31-,33+,34+,35-/m0/s1
InChI Key ZVYBIARXHLUXGT-IVADFWPZSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C35H42O10
Molecular Weight 622.70 g/mol
Exact Mass 622.27779753 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.54
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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CHEMBL468680

2D Structure

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2D Structure of Taxinine NN-4

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9889 98.89%
Caco-2 - 0.8159 81.59%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6102 61.02%
OATP2B1 inhibitior - 0.7168 71.68%
OATP1B1 inhibitior + 0.8241 82.41%
OATP1B3 inhibitior + 0.9191 91.91%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9660 96.60%
P-glycoprotein inhibitior + 0.8794 87.94%
P-glycoprotein substrate - 0.6951 69.51%
CYP3A4 substrate + 0.6862 68.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition + 0.6628 66.28%
CYP2C9 inhibition - 0.7715 77.15%
CYP2C19 inhibition - 0.6380 63.80%
CYP2D6 inhibition - 0.8748 87.48%
CYP1A2 inhibition - 0.5728 57.28%
CYP2C8 inhibition + 0.7492 74.92%
CYP inhibitory promiscuity - 0.7836 78.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9061 90.61%
Carcinogenicity (trinary) Non-required 0.5890 58.90%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.8949 89.49%
Skin irritation - 0.6611 66.11%
Skin corrosion - 0.9213 92.13%
Ames mutagenesis - 0.5828 58.28%
Human Ether-a-go-go-Related Gene inhibition + 0.7768 77.68%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation - 0.5956 59.56%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7040 70.40%
Acute Oral Toxicity (c) III 0.5389 53.89%
Estrogen receptor binding + 0.7796 77.96%
Androgen receptor binding + 0.7693 76.93%
Thyroid receptor binding + 0.6764 67.64%
Glucocorticoid receptor binding + 0.7913 79.13%
Aromatase binding + 0.6909 69.09%
PPAR gamma + 0.7954 79.54%
Honey bee toxicity - 0.7827 78.27%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9962 99.62%

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 98.64% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.97% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 94.97% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.65% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.83% 95.50%
CHEMBL3524 P56524 Histone deacetylase 4 91.49% 92.97%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.99% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.50% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.37% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 87.95% 83.82%
CHEMBL2581 P07339 Cathepsin D 87.60% 98.95%
CHEMBL5028 O14672 ADAM10 87.59% 97.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.97% 94.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.82% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 85.51% 91.49%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.42% 93.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.96% 85.14%
CHEMBL1937 Q92769 Histone deacetylase 2 84.92% 94.75%
CHEMBL340 P08684 Cytochrome P450 3A4 84.28% 91.19%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 80.82% 83.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.54% 89.00%

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 canadensis
Taxus cuspidata

Cross-Links

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PubChem 15895528
NPASS NPC184109
LOTUS LTS0231971
wikiData Q105384755