[(3R,3aS,4S,8R,8aS)-3-hydroxy-6,8a-dimethyl-8-[(Z)-2-methylbut-2-enoyl]oxy-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] 4-hydroxybenzoate

Details

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Internal ID d74363ff-94e7-4eed-a499-7c4fef773eb4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [(3R,3aS,4S,8R,8aS)-3-hydroxy-6,8a-dimethyl-8-[(Z)-2-methylbut-2-enoyl]oxy-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] 4-hydroxybenzoate
SMILES (Canonical) CC=C(C)C(=O)OC1C=C(CC(C2C1(CCC2(C(C)C)O)C)OC(=O)C3=CC=C(C=C3)O)C
SMILES (Isomeric) C/C=C(/C)\C(=O)O[C@@H]1C=C(C[C@@H]([C@@H]2[C@@]1(CC[C@]2(C(C)C)O)C)OC(=O)C3=CC=C(C=C3)O)C
InChI InChI=1S/C27H36O6/c1-7-18(5)24(29)33-22-15-17(4)14-21(32-25(30)19-8-10-20(28)11-9-19)23-26(22,6)12-13-27(23,31)16(2)3/h7-11,15-16,21-23,28,31H,12-14H2,1-6H3/b18-7-/t21-,22+,23+,26+,27+/m0/s1
InChI Key NUXKLJINNAOFAH-KIBFMCBCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H36O6
Molecular Weight 456.60 g/mol
Exact Mass 456.25118886 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.95
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(3R,3aS,4S,8R,8aS)-3-hydroxy-6,8a-dimethyl-8-[(Z)-2-methylbut-2-enoyl]oxy-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] 4-hydroxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 - 0.5644 56.44%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7770 77.70%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.8086 80.86%
OATP1B3 inhibitior - 0.3198 31.98%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7321 73.21%
BSEP inhibitior + 0.9372 93.72%
P-glycoprotein inhibitior + 0.8122 81.22%
P-glycoprotein substrate + 0.5978 59.78%
CYP3A4 substrate + 0.6864 68.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8732 87.32%
CYP3A4 inhibition - 0.8202 82.02%
CYP2C9 inhibition + 0.6260 62.60%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.9366 93.66%
CYP1A2 inhibition + 0.6502 65.02%
CYP2C8 inhibition + 0.6397 63.97%
CYP inhibitory promiscuity - 0.8829 88.29%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5768 57.68%
Eye corrosion - 0.9929 99.29%
Eye irritation - 0.9165 91.65%
Skin irritation - 0.5220 52.20%
Skin corrosion - 0.9274 92.74%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6651 66.51%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.5238 52.38%
skin sensitisation - 0.6995 69.95%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.6917 69.17%
Acute Oral Toxicity (c) II 0.3886 38.86%
Estrogen receptor binding + 0.7261 72.61%
Androgen receptor binding + 0.6661 66.61%
Thyroid receptor binding + 0.6012 60.12%
Glucocorticoid receptor binding + 0.7867 78.67%
Aromatase binding + 0.6026 60.26%
PPAR gamma + 0.6607 66.07%
Honey bee toxicity - 0.8056 80.56%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9973 99.73%

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
CHEMBL2581 P07339 Cathepsin D 94.62% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.08% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.65% 91.11%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 92.11% 97.21%
CHEMBL245 P20309 Muscarinic acetylcholine receptor M3 89.72% 97.53%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.47% 95.89%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 88.46% 94.97%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.36% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.91% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 86.18% 91.19%
CHEMBL221 P23219 Cyclooxygenase-1 85.93% 90.17%
CHEMBL2996 Q05655 Protein kinase C delta 85.81% 97.79%
CHEMBL4208 P20618 Proteasome component C5 85.21% 90.00%
CHEMBL284 P27487 Dipeptidyl peptidase IV 84.79% 95.69%
CHEMBL2535 P11166 Glucose transporter 84.61% 98.75%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 84.43% 85.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.38% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.84% 89.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.53% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.36% 100.00%
CHEMBL242 Q92731 Estrogen receptor beta 80.02% 98.35%

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 communis

Cross-Links

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PubChem 14239533
LOTUS LTS0088456
wikiData Q105186082