4alpha-Methylcadinane-1alpha,2alpha,10alpha triol

Details

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Internal ID 6758c332-38a1-40b4-98be-08d5a16052a5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,3S,4aS,5S,8R,8aR)-3,8-dimethyl-5-propan-2-yl-1,2,3,4,4a,5,6,7-octahydronaphthalene-1,8,8a-triol
SMILES (Canonical) CC1CC2C(CCC(C2(C(C1)O)O)(C)O)C(C)C
SMILES (Isomeric) C[C@H]1C[C@H]2[C@@H](CC[C@@]([C@@]2([C@H](C1)O)O)(C)O)C(C)C
InChI InChI=1S/C15H28O3/c1-9(2)11-5-6-14(4,17)15(18)12(11)7-10(3)8-13(15)16/h9-13,16-18H,5-8H2,1-4H3/t10-,11-,12-,13-,14+,15+/m0/s1
InChI Key NOMPOPNILJKBDF-GXYBRJDSSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H28O3
Molecular Weight 256.38 g/mol
Exact Mass 256.20384475 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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4alpha-methylcadinane-1alpha,2alpha,10alpha triol

2D Structure

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2D Structure of 4alpha-Methylcadinane-1alpha,2alpha,10alpha triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9772 97.72%
Caco-2 - 0.5303 53.03%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5963 59.63%
OATP2B1 inhibitior - 0.8469 84.69%
OATP1B1 inhibitior + 0.9534 95.34%
OATP1B3 inhibitior + 0.9558 95.58%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8906 89.06%
P-glycoprotein inhibitior - 0.9418 94.18%
P-glycoprotein substrate - 0.7868 78.68%
CYP3A4 substrate + 0.5806 58.06%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.7068 70.68%
CYP3A4 inhibition - 0.8877 88.77%
CYP2C9 inhibition - 0.7969 79.69%
CYP2C19 inhibition - 0.7789 77.89%
CYP2D6 inhibition - 0.9611 96.11%
CYP1A2 inhibition - 0.7288 72.88%
CYP2C8 inhibition - 0.9005 90.05%
CYP inhibitory promiscuity - 0.9648 96.48%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6530 65.30%
Eye corrosion - 0.9848 98.48%
Eye irritation - 0.5601 56.01%
Skin irritation + 0.5182 51.82%
Skin corrosion - 0.8980 89.80%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6602 66.02%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5779 57.79%
skin sensitisation - 0.6576 65.76%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.7188 71.88%
Acute Oral Toxicity (c) III 0.6205 62.05%
Estrogen receptor binding + 0.6185 61.85%
Androgen receptor binding + 0.5980 59.80%
Thyroid receptor binding + 0.6404 64.04%
Glucocorticoid receptor binding - 0.5070 50.70%
Aromatase binding - 0.5822 58.22%
PPAR gamma - 0.7363 73.63%
Honey bee toxicity - 0.7685 76.85%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9378 93.78%

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 98.36% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.14% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 90.21% 97.79%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.84% 97.09%
CHEMBL206 P03372 Estrogen receptor alpha 89.51% 97.64%
CHEMBL226 P30542 Adenosine A1 receptor 88.29% 95.93%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.11% 100.00%
CHEMBL299 P17252 Protein kinase C alpha 88.09% 98.03%
CHEMBL1937 Q92769 Histone deacetylase 2 86.95% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.61% 94.45%
CHEMBL259 P32245 Melanocortin receptor 4 86.26% 95.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.22% 82.69%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.00% 85.14%
CHEMBL1871 P10275 Androgen Receptor 83.45% 96.43%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.79% 92.86%
CHEMBL4072 P07858 Cathepsin B 82.27% 93.67%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.02% 90.08%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.61% 100.00%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 81.55% 95.58%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.30% 96.61%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.68% 91.03%

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.
Taiwania cryptomerioides

Cross-Links

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PubChem 10801091
LOTUS LTS0059673
wikiData Q105182644