(3S,6R)-6-methoxy-3-(methoxymethyl)-7-methylocta-1,7-dien-3-ol

Details

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Internal ID 97f5cd80-0d8d-4339-a4f1-e680573a243d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (3S,6R)-6-methoxy-3-(methoxymethyl)-7-methylocta-1,7-dien-3-ol
SMILES (Canonical) CC(=C)C(CCC(COC)(C=C)O)OC
SMILES (Isomeric) CC(=C)[C@@H](CC[C@@](COC)(C=C)O)OC
InChI InChI=1S/C12H22O3/c1-6-12(13,9-14-4)8-7-11(15-5)10(2)3/h6,11,13H,1-2,7-9H2,3-5H3/t11-,12-/m1/s1
InChI Key YVORMDDFZMHTHT-VXGBXAGGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H22O3
Molecular Weight 214.30 g/mol
Exact Mass 214.15689456 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.92
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,6R)-6-methoxy-3-(methoxymethyl)-7-methylocta-1,7-dien-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9788 97.88%
Caco-2 + 0.5343 53.43%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6210 62.10%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.9222 92.22%
OATP1B3 inhibitior + 0.9584 95.84%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8291 82.91%
BSEP inhibitior - 0.8970 89.70%
P-glycoprotein inhibitior - 0.9596 95.96%
P-glycoprotein substrate - 0.8533 85.33%
CYP3A4 substrate - 0.5141 51.41%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate - 0.7578 75.78%
CYP3A4 inhibition - 0.7322 73.22%
CYP2C9 inhibition - 0.8549 85.49%
CYP2C19 inhibition - 0.8252 82.52%
CYP2D6 inhibition - 0.9268 92.68%
CYP1A2 inhibition - 0.8352 83.52%
CYP2C8 inhibition - 0.8872 88.72%
CYP inhibitory promiscuity - 0.9407 94.07%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6689 66.89%
Eye corrosion - 0.8871 88.71%
Eye irritation - 0.5955 59.55%
Skin irritation - 0.6170 61.70%
Skin corrosion - 0.9564 95.64%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5298 52.98%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5967 59.67%
skin sensitisation + 0.6590 65.90%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6393 63.93%
Acute Oral Toxicity (c) III 0.6501 65.01%
Estrogen receptor binding - 0.6341 63.41%
Androgen receptor binding - 0.6802 68.02%
Thyroid receptor binding - 0.6309 63.09%
Glucocorticoid receptor binding + 0.5660 56.60%
Aromatase binding - 0.7337 73.37%
PPAR gamma - 0.6622 66.22%
Honey bee toxicity - 0.5660 56.60%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.4330 43.30%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.46% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.49% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.37% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.62% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.79% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.15% 85.14%

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 163060595
LOTUS LTS0057290
wikiData Q105365758