7-Megastigmene-3,5,6,9-tetraol

Details

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Internal ID d6347fc1-c03c-42a4-a4df-6ce8418e39fa
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,2R,4S)-1-[(E,3S)-3-hydroxybut-1-enyl]-2,6,6-trimethylcyclohexane-1,2,4-triol
SMILES (Canonical) CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)O
SMILES (Isomeric) C[C@@H](/C=C/[C@@]1([C@](C[C@H](CC1(C)C)O)(C)O)O)O
InChI InChI=1S/C13H24O4/c1-9(14)5-6-13(17)11(2,3)7-10(15)8-12(13,4)16/h5-6,9-10,14-17H,7-8H2,1-4H3/b6-5+/t9-,10-,12+,13+/m0/s1
InChI Key CTCKPFXFWVNGLG-DWFSUXBBSA-N
Popularity 73 references in papers

Physical and Chemical Properties

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Molecular Formula C13H24O4
Molecular Weight 244.33 g/mol
Exact Mass 244.16745924 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.59
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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Megastigmane
Megastigm-7-ene-3,5,6,9-tetraol
276870-26-9
CHEMBL1643084
AKOS040762570
(1R,2R,4S)-1-[(E,3S)-3-hydroxybut-1-enyl]-2,6,6-trimethylcyclohexane-1,2,4-triol
(1R)-1-[(1E,3S)-3-Hydroxy-1-butenyl]-2,6,6-trimethylcyclohexane-1beta,2alpha,4beta-triol

2D Structure

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2D Structure of 7-Megastigmene-3,5,6,9-tetraol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8672 86.72%
Caco-2 + 0.5573 55.73%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6551 65.51%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9500 95.00%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8579 85.79%
P-glycoprotein inhibitior - 0.9640 96.40%
P-glycoprotein substrate - 0.8888 88.88%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 0.7872 78.72%
CYP2D6 substrate - 0.7834 78.34%
CYP3A4 inhibition - 0.8546 85.46%
CYP2C9 inhibition - 0.8809 88.09%
CYP2C19 inhibition - 0.8544 85.44%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.8660 86.60%
CYP2C8 inhibition - 0.9686 96.86%
CYP inhibitory promiscuity - 0.9591 95.91%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6205 62.05%
Eye corrosion - 0.9759 97.59%
Eye irritation - 0.6436 64.36%
Skin irritation - 0.6268 62.68%
Skin corrosion - 0.8591 85.91%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7795 77.95%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.5600 56.00%
skin sensitisation + 0.4739 47.39%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7976 79.76%
Acute Oral Toxicity (c) III 0.6457 64.57%
Estrogen receptor binding - 0.6631 66.31%
Androgen receptor binding - 0.5230 52.30%
Thyroid receptor binding + 0.6446 64.46%
Glucocorticoid receptor binding - 0.4655 46.55%
Aromatase binding - 0.6324 63.24%
PPAR gamma - 0.7337 73.37%
Honey bee toxicity - 0.7522 75.22%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.8595 85.95%

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 94.47% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.92% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 93.73% 90.17%
CHEMBL2179 P04062 Beta-glucocerebrosidase 87.99% 85.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.90% 85.14%
CHEMBL284 P27487 Dipeptidyl peptidase IV 85.52% 95.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.58% 91.11%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.76% 92.86%

Cross-Links

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PubChem 637237
NPASS NPC26020
LOTUS LTS0168650
wikiData Q104969707