[(1R,3aR,5S,6R,8aS)-6,8a-dihydroxy-3a,6-dimethyl-1-propan-2-yl-2,3,4,5,7,8-hexahydro-1H-azulen-5-yl] 3,4,5-trimethoxybenzoate

Details

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Internal ID 69abf8bb-4708-4cd8-90cf-040a5460656f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [(1R,3aR,5S,6R,8aS)-6,8a-dihydroxy-3a,6-dimethyl-1-propan-2-yl-2,3,4,5,7,8-hexahydro-1H-azulen-5-yl] 3,4,5-trimethoxybenzoate
SMILES (Canonical) CC(C)C1CCC2(C1(CCC(C(C2)OC(=O)C3=CC(=C(C(=C3)OC)OC)OC)(C)O)O)C
SMILES (Isomeric) CC(C)[C@H]1CC[C@]2([C@@]1(CC[C@@]([C@H](C2)OC(=O)C3=CC(=C(C(=C3)OC)OC)OC)(C)O)O)C
InChI InChI=1S/C25H38O7/c1-15(2)17-8-9-23(3)14-20(24(4,27)10-11-25(17,23)28)32-22(26)16-12-18(29-5)21(31-7)19(13-16)30-6/h12-13,15,17,20,27-28H,8-11,14H2,1-7H3/t17-,20+,23-,24-,25+/m1/s1
InChI Key MXZWEUNFKTYREI-FGLAVKMOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H38O7
Molecular Weight 450.60 g/mol
Exact Mass 450.26175355 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,3aR,5S,6R,8aS)-6,8a-dihydroxy-3a,6-dimethyl-1-propan-2-yl-2,3,4,5,7,8-hexahydro-1H-azulen-5-yl] 3,4,5-trimethoxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.5700 57.00%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7937 79.37%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.9239 92.39%
OATP1B3 inhibitior + 0.8083 80.83%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8571 85.71%
BSEP inhibitior + 0.6765 67.65%
P-glycoprotein inhibitior + 0.6318 63.18%
P-glycoprotein substrate - 0.6058 60.58%
CYP3A4 substrate + 0.6461 64.61%
CYP2C9 substrate - 0.5698 56.98%
CYP2D6 substrate - 0.8011 80.11%
CYP3A4 inhibition - 0.7575 75.75%
CYP2C9 inhibition + 0.5858 58.58%
CYP2C19 inhibition + 0.5985 59.85%
CYP2D6 inhibition - 0.9516 95.16%
CYP1A2 inhibition + 0.8548 85.48%
CYP2C8 inhibition + 0.5398 53.98%
CYP inhibitory promiscuity - 0.9659 96.59%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6197 61.97%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9297 92.97%
Skin irritation - 0.5583 55.83%
Skin corrosion - 0.9402 94.02%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4527 45.27%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.6790 67.90%
skin sensitisation - 0.8497 84.97%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.8199 81.99%
Acute Oral Toxicity (c) II 0.3253 32.53%
Estrogen receptor binding + 0.7436 74.36%
Androgen receptor binding + 0.6441 64.41%
Thyroid receptor binding + 0.6397 63.97%
Glucocorticoid receptor binding + 0.7511 75.11%
Aromatase binding + 0.8323 83.23%
PPAR gamma + 0.6271 62.71%
Honey bee toxicity - 0.8298 82.98%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5936 59.36%
Fish aquatic toxicity + 0.9891 98.91%

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 97.33% 96.09%
CHEMBL4302 P08183 P-glycoprotein 1 97.07% 92.98%
CHEMBL2179 P04062 Beta-glucocerebrosidase 94.08% 85.31%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 92.51% 96.38%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 92.31% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 91.02% 91.19%
CHEMBL2535 P11166 Glucose transporter 89.58% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.67% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.44% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.11% 91.11%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.05% 91.07%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.74% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.63% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.86% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.50% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.46% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.97% 92.62%
CHEMBL1871 P10275 Androgen Receptor 81.75% 96.43%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.64% 99.18%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.25% 89.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.12% 99.17%

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.
Ferula pallida

Cross-Links

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PubChem 163043599
LOTUS LTS0270918
wikiData Q105174731