2-(4-Hydroxy-3,7-dimethylocta-2,6-dienoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

Details

Top
Internal ID 49e6f4f9-5280-4a59-bfb1-b02714fb03a7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name 2-(4-hydroxy-3,7-dimethylocta-2,6-dienoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) CC(=CCC(C(=CCOC1C(C(C(C(O1)CO)O)O)O)C)O)C
SMILES (Isomeric) CC(=CCC(C(=CCOC1C(C(C(C(O1)CO)O)O)O)C)O)C
InChI InChI=1S/C16H28O7/c1-9(2)4-5-11(18)10(3)6-7-22-16-15(21)14(20)13(19)12(8-17)23-16/h4,6,11-21H,5,7-8H2,1-3H3
InChI Key PBPYEEMQIFDGSQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H28O7
Molecular Weight 332.39 g/mol
Exact Mass 332.18350323 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP 0.10
Atomic LogP (AlogP) -0.53
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 7

Synonyms

Top
100462-37-1
PD087380
FT-0686696

2D Structure

Top
2D Structure of 2-(4-Hydroxy-3,7-dimethylocta-2,6-dienoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6322 63.22%
Caco-2 - 0.8757 87.57%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7987 79.87%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9003 90.03%
OATP1B3 inhibitior + 0.9398 93.98%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9523 95.23%
P-glycoprotein inhibitior - 0.9182 91.82%
P-glycoprotein substrate - 0.9384 93.84%
CYP3A4 substrate + 0.5225 52.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8353 83.53%
CYP3A4 inhibition - 0.9730 97.30%
CYP2C9 inhibition - 0.8963 89.63%
CYP2C19 inhibition - 0.8498 84.98%
CYP2D6 inhibition - 0.8885 88.85%
CYP1A2 inhibition - 0.8773 87.73%
CYP2C8 inhibition - 0.8589 85.89%
CYP inhibitory promiscuity - 0.9453 94.53%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7564 75.64%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9858 98.58%
Skin irritation - 0.8161 81.61%
Skin corrosion - 0.9612 96.12%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5956 59.56%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.7416 74.16%
skin sensitisation - 0.8487 84.87%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.4767 47.67%
Acute Oral Toxicity (c) III 0.5884 58.84%
Estrogen receptor binding - 0.6204 62.04%
Androgen receptor binding - 0.6967 69.67%
Thyroid receptor binding + 0.6119 61.19%
Glucocorticoid receptor binding - 0.6258 62.58%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.5379 53.79%
Honey bee toxicity - 0.7748 77.48%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.9600 96.00%
Fish aquatic toxicity - 0.3937 39.37%

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 94.65% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.40% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.83% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 88.96% 94.73%
CHEMBL2581 P07339 Cathepsin D 87.44% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.66% 86.92%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.77% 97.25%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 80.94% 97.34%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.61% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.40% 99.17%

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.
Rhodiola kirilowii
Rhodiola rosea

Cross-Links

Top
PubChem 73181367
LOTUS LTS0048062
wikiData Q105205351