(3S,6S)-3,6-dimethoxy-1-methyl-4-propan-2-ylcyclohexa-1,4-diene

Details

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Internal ID 1d0cb459-a8d1-4883-b7eb-8cae253212b5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name (3S,6S)-3,6-dimethoxy-1-methyl-4-propan-2-ylcyclohexa-1,4-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H20O2/c1-8(2)10-7-11(13-4)9(3)6-12(10)14-5/h6-8,11-12H,1-5H3/t11-,12-/m0/s1
InChI Key FLFQAMVYBHKCNO-RYUDHWBXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O2
Molecular Weight 196.29 g/mol
Exact Mass 196.146329876 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.56
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,6S)-3,6-dimethoxy-1-methyl-4-propan-2-ylcyclohexa-1,4-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.8329 83.29%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7457 74.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9411 94.11%
OATP1B3 inhibitior + 0.9723 97.23%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9497 94.97%
P-glycoprotein inhibitior - 0.9272 92.72%
P-glycoprotein substrate - 0.9068 90.68%
CYP3A4 substrate - 0.6632 66.32%
CYP2C9 substrate - 0.7698 76.98%
CYP2D6 substrate - 0.7685 76.85%
CYP3A4 inhibition - 0.8603 86.03%
CYP2C9 inhibition - 0.9435 94.35%
CYP2C19 inhibition - 0.7041 70.41%
CYP2D6 inhibition - 0.9384 93.84%
CYP1A2 inhibition - 0.8004 80.04%
CYP2C8 inhibition - 0.9486 94.86%
CYP inhibitory promiscuity + 0.5325 53.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6339 63.39%
Carcinogenicity (trinary) Non-required 0.5590 55.90%
Eye corrosion - 0.6428 64.28%
Eye irritation + 0.7541 75.41%
Skin irritation - 0.5913 59.13%
Skin corrosion - 0.9877 98.77%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6034 60.34%
skin sensitisation + 0.7526 75.26%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.6216 62.16%
Acute Oral Toxicity (c) III 0.7598 75.98%
Estrogen receptor binding - 0.9093 90.93%
Androgen receptor binding - 0.6798 67.98%
Thyroid receptor binding - 0.7717 77.17%
Glucocorticoid receptor binding - 0.9014 90.14%
Aromatase binding - 0.7978 79.78%
PPAR gamma - 0.8297 82.97%
Honey bee toxicity - 0.7633 76.33%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.7770 77.70%

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 87.75% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.83% 94.45%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.98% 93.65%
CHEMBL2581 P07339 Cathepsin D 82.89% 98.95%

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.
Blumea viscosa

Cross-Links

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PubChem 162982358
LOTUS LTS0266219
wikiData Q104997034