cis-Muurol-5-en-4-beta-ol

Details

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Internal ID 4ba17d4c-a1f7-4844-b571-a5e9cebfaa17
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,4S)-4,7-dimethyl-1-propan-2-yl-3,4,4a,5,6,7-hexahydro-2H-naphthalen-1-ol
SMILES (Canonical) CC1CCC2C(CCC(C2=C1)(C(C)C)O)C
SMILES (Isomeric) C[C@H]1CC[C@@](C2=CC(CCC12)C)(C(C)C)O
InChI InChI=1S/C15H26O/c1-10(2)15(16)8-7-12(4)13-6-5-11(3)9-14(13)15/h9-13,16H,5-8H2,1-4H3/t11?,12-,13?,15-/m0/s1
InChI Key UAJHVFUBIKCODA-GWIFJHRUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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UAJHVFUBIKCODA-GWIFJHRUSA-N

2D Structure

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2D Structure of cis-Muurol-5-en-4-beta-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8144 81.44%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.4916 49.16%
OATP2B1 inhibitior - 0.8405 84.05%
OATP1B1 inhibitior + 0.9345 93.45%
OATP1B3 inhibitior + 0.9707 97.07%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9330 93.30%
P-glycoprotein inhibitior - 0.9590 95.90%
P-glycoprotein substrate - 0.8585 85.85%
CYP3A4 substrate - 0.5253 52.53%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7267 72.67%
CYP3A4 inhibition - 0.8938 89.38%
CYP2C9 inhibition - 0.6800 68.00%
CYP2C19 inhibition - 0.5822 58.22%
CYP2D6 inhibition - 0.9281 92.81%
CYP1A2 inhibition - 0.8433 84.33%
CYP2C8 inhibition - 0.9226 92.26%
CYP inhibitory promiscuity - 0.8281 82.81%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5747 57.47%
Eye corrosion - 0.9803 98.03%
Eye irritation - 0.7675 76.75%
Skin irritation + 0.6295 62.95%
Skin corrosion - 0.9473 94.73%
Ames mutagenesis - 0.7570 75.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5077 50.77%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5307 53.07%
skin sensitisation + 0.6615 66.15%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7616 76.16%
Acute Oral Toxicity (c) III 0.8227 82.27%
Estrogen receptor binding - 0.8923 89.23%
Androgen receptor binding - 0.6898 68.98%
Thyroid receptor binding - 0.6511 65.11%
Glucocorticoid receptor binding - 0.6911 69.11%
Aromatase binding - 0.7459 74.59%
PPAR gamma - 0.8809 88.09%
Honey bee toxicity - 0.9503 95.03%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9772 97.72%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.88% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.03% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.91% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.01% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.64% 94.45%
CHEMBL2581 P07339 Cathepsin D 82.57% 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.
Teucrium leucocladum

Cross-Links

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PubChem 6428412
LOTUS LTS0208530
wikiData Q105268847