6-[(2-Hydroxy-5-methoxy-3-methylphenyl)methyl]-2,5,6,11,11-pentamethyl-12,13-dioxatricyclo[8.6.0.02,7]hexadec-1(10)-en-14-one

Details

Top
Internal ID 4f3c93f8-0d5f-4a81-a679-a2deee89f660
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 6-[(2-hydroxy-5-methoxy-3-methylphenyl)methyl]-2,5,6,11,11-pentamethyl-12,13-dioxatricyclo[8.6.0.02,7]hexadec-1(10)-en-14-one
SMILES (Canonical) CC1CCC2(C(C1(C)CC3=C(C(=CC(=C3)OC)C)O)CCC4=C2CCC(=O)OOC4(C)C)C
SMILES (Isomeric) CC1CCC2(C(C1(C)CC3=C(C(=CC(=C3)OC)C)O)CCC4=C2CCC(=O)OOC4(C)C)C
InChI InChI=1S/C28H40O5/c1-17-14-20(31-7)15-19(25(17)30)16-28(6)18(2)12-13-27(5)22-9-11-24(29)32-33-26(3,4)21(22)8-10-23(27)28/h14-15,18,23,30H,8-13,16H2,1-7H3
InChI Key ZVDQLQRXHLAXOG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C28H40O5
Molecular Weight 456.60 g/mol
Exact Mass 456.28757437 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 6.20
Atomic LogP (AlogP) 6.45
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 6-[(2-Hydroxy-5-methoxy-3-methylphenyl)methyl]-2,5,6,11,11-pentamethyl-12,13-dioxatricyclo[8.6.0.02,7]hexadec-1(10)-en-14-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.6383 63.83%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7496 74.96%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.8148 81.48%
OATP1B3 inhibitior - 0.2987 29.87%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9508 95.08%
P-glycoprotein inhibitior + 0.7255 72.55%
P-glycoprotein substrate - 0.7543 75.43%
CYP3A4 substrate + 0.6706 67.06%
CYP2C9 substrate - 0.5839 58.39%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition + 0.5064 50.64%
CYP2C9 inhibition - 0.6788 67.88%
CYP2C19 inhibition - 0.6261 62.61%
CYP2D6 inhibition - 0.8969 89.69%
CYP1A2 inhibition - 0.6026 60.26%
CYP2C8 inhibition + 0.5690 56.90%
CYP inhibitory promiscuity - 0.7573 75.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8643 86.43%
Carcinogenicity (trinary) Non-required 0.6171 61.71%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.8619 86.19%
Skin irritation - 0.7185 71.85%
Skin corrosion - 0.9515 95.15%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7454 74.54%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.6391 63.91%
skin sensitisation - 0.8044 80.44%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.5589 55.89%
Acute Oral Toxicity (c) IV 0.4409 44.09%
Estrogen receptor binding + 0.7890 78.90%
Androgen receptor binding + 0.6676 66.76%
Thyroid receptor binding + 0.6936 69.36%
Glucocorticoid receptor binding + 0.8299 82.99%
Aromatase binding + 0.8366 83.66%
PPAR gamma + 0.6525 65.25%
Honey bee toxicity - 0.8358 83.58%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9974 99.74%

Targets

Top

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 99.38% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.18% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.81% 98.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.36% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.31% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.95% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.35% 96.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.76% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.04% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.45% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.76% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.13% 92.94%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.07% 93.40%
CHEMBL4581 P52732 Kinesin-like protein 1 85.24% 93.18%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.03% 89.00%
CHEMBL4530 P00488 Coagulation factor XIII 84.67% 96.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.55% 96.77%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.37% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.40% 85.14%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.30% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.17% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.47% 90.71%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 74051433
LOTUS LTS0146129
wikiData Q105384221