[(1S,2S,3E,5S,7S,8R,10R,13S)-2,13-diacetyloxy-7,10-dihydroxy-8,12,15,15-tetramethyl-9-oxo-5-tricyclo[9.3.1.14,8]hexadeca-3,11-dienyl] (2R,3S)-3-(dimethylamino)-2-hydroxy-3-phenylpropanoate

Details

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Internal ID a3c6edf8-03e3-43b7-816a-45368dd4dab7
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name [(1S,2S,3E,5S,7S,8R,10R,13S)-2,13-diacetyloxy-7,10-dihydroxy-8,12,15,15-tetramethyl-9-oxo-5-tricyclo[9.3.1.14,8]hexadeca-3,11-dienyl] (2R,3S)-3-(dimethylamino)-2-hydroxy-3-phenylpropanoate
SMILES (Canonical) CC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C)OC(=O)C)C(CC3O)OC(=O)C(C(C4=CC=CC=C4)N(C)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)OC(=O)C)/[C@H](C[C@@H]3O)OC(=O)[C@@H]([C@H](C4=CC=CC=C4)N(C)C)O)C)O
InChI InChI=1S/C35H47NO10/c1-18-24(44-19(2)37)15-23-26(45-20(3)38)14-22-17-35(6,32(42)30(40)28(18)34(23,4)5)27(39)16-25(22)46-33(43)31(41)29(36(7)8)21-12-10-9-11-13-21/h9-14,23-27,29-31,39-41H,15-17H2,1-8H3/b22-14+/t23-,24+,25+,26+,27+,29+,30-,31-,35-/m1/s1
InChI Key KOTXAHKUCAQPQA-CBBMDTEMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C35H47NO10
Molecular Weight 641.70 g/mol
Exact Mass 641.31999670 g/mol
Topological Polar Surface Area (TPSA) 160.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.82
H-Bond Acceptor 11
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2S,3E,5S,7S,8R,10R,13S)-2,13-diacetyloxy-7,10-dihydroxy-8,12,15,15-tetramethyl-9-oxo-5-tricyclo[9.3.1.14,8]hexadeca-3,11-dienyl] (2R,3S)-3-(dimethylamino)-2-hydroxy-3-phenylpropanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9784 97.84%
Caco-2 - 0.8161 81.61%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6508 65.08%
OATP2B1 inhibitior + 0.5673 56.73%
OATP1B1 inhibitior + 0.8133 81.33%
OATP1B3 inhibitior + 0.9136 91.36%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9749 97.49%
P-glycoprotein inhibitior + 0.8276 82.76%
P-glycoprotein substrate + 0.6477 64.77%
CYP3A4 substrate + 0.7260 72.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7096 70.96%
CYP3A4 inhibition - 0.6142 61.42%
CYP2C9 inhibition - 0.8231 82.31%
CYP2C19 inhibition - 0.8185 81.85%
CYP2D6 inhibition - 0.8583 85.83%
CYP1A2 inhibition - 0.6952 69.52%
CYP2C8 inhibition + 0.5580 55.80%
CYP inhibitory promiscuity - 0.9030 90.30%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4825 48.25%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.9271 92.71%
Skin irritation - 0.7408 74.08%
Skin corrosion - 0.9320 93.20%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5434 54.34%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5283 52.83%
skin sensitisation - 0.8326 83.26%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.6856 68.56%
Acute Oral Toxicity (c) III 0.5455 54.55%
Estrogen receptor binding + 0.7766 77.66%
Androgen receptor binding + 0.7080 70.80%
Thyroid receptor binding + 0.5652 56.52%
Glucocorticoid receptor binding + 0.8168 81.68%
Aromatase binding + 0.6549 65.49%
PPAR gamma + 0.7769 77.69%
Honey bee toxicity - 0.5528 55.28%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9875 98.75%

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 97.99% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.77% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.52% 85.14%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 97.38% 94.62%
CHEMBL4040 P28482 MAP kinase ERK2 97.32% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.01% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.63% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 92.48% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.06% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.44% 89.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 90.03% 94.08%
CHEMBL340 P08684 Cytochrome P450 3A4 89.19% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.45% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.15% 86.33%
CHEMBL5028 O14672 ADAM10 86.52% 97.50%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 81.30% 89.44%

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 163188092
LOTUS LTS0014970
wikiData Q105143994