Bis(6-(3,4,7-trihydroxy-3, 7-dimethyloctenyl) ether

Details

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Internal ID 56f155bf-3723-4c5f-8e79-4775b6006bcb
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 2,6-dimethyl-3-(2,5,6-trihydroxy-2,6-dimethyloct-7-en-3-yl)oxyoct-7-ene-2,5,6-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H38O7/c1-9-19(7,25)13(21)11-15(17(3,4)23)27-16(18(5,6)24)12-14(22)20(8,26)10-2/h9-10,13-16,21-26H,1-2,11-12H2,3-8H3
InChI Key AFYKJKWLNLIKRG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H38O7
Molecular Weight 390.50 g/mol
Exact Mass 390.26175355 g/mol
Topological Polar Surface Area (TPSA) 131.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.66
H-Bond Acceptor 7
H-Bond Donor 6
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Bis(6-(3,4,7-trihydroxy-3, 7-dimethyloctenyl) ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9517 95.17%
Caco-2 - 0.7910 79.10%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7097 70.97%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9361 93.61%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7871 78.71%
P-glycoprotein inhibitior - 0.6550 65.50%
P-glycoprotein substrate - 0.9461 94.61%
CYP3A4 substrate - 0.5832 58.32%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.7624 76.24%
CYP3A4 inhibition - 0.8691 86.91%
CYP2C9 inhibition - 0.8536 85.36%
CYP2C19 inhibition - 0.7737 77.37%
CYP2D6 inhibition - 0.9276 92.76%
CYP1A2 inhibition - 0.8799 87.99%
CYP2C8 inhibition - 0.9059 90.59%
CYP inhibitory promiscuity - 0.9405 94.05%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.7078 70.78%
Eye corrosion - 0.8990 89.90%
Eye irritation - 0.8617 86.17%
Skin irritation - 0.5999 59.99%
Skin corrosion - 0.9180 91.80%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6597 65.97%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6783 67.83%
skin sensitisation + 0.5729 57.29%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5143 51.43%
Acute Oral Toxicity (c) III 0.6936 69.36%
Estrogen receptor binding + 0.7572 75.72%
Androgen receptor binding - 0.7087 70.87%
Thyroid receptor binding + 0.6822 68.22%
Glucocorticoid receptor binding + 0.7519 75.19%
Aromatase binding + 0.6959 69.59%
PPAR gamma + 0.7697 76.97%
Honey bee toxicity - 0.6590 65.90%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7731 77.31%
Fish aquatic toxicity + 0.8019 80.19%

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 91.45% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.74% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.58% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.11% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 84.25% 94.73%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.58% 97.29%
CHEMBL4662 P28074 Proteasome Macropain subunit MB1 80.82% 93.85%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.27% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 15895325
LOTUS LTS0019205
wikiData Q77381300