Isocadinanol A

Details

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Internal ID 99f26098-2731-405d-80b9-f227a40ede4f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (1aR,2R,4aS,5R,6R,8R,8aS)-1a,5-dimethyl-8-propan-2-yl-2,3,4,4a,5,6,7,8-octahydronaphtho[1,8a-b]oxirene-2,6-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O3/c1-8(2)11-7-12(16)9(3)10-5-6-13(17)14(4)15(10,11)18-14/h8-13,16-17H,5-7H2,1-4H3/t9-,10+,11-,12-,13-,14-,15-/m1/s1
InChI Key KALHVLRQNHIJOX-CVEQBJKISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O3
Molecular Weight 254.36 g/mol
Exact Mass 254.18819469 g/mol
Topological Polar Surface Area (TPSA) 53.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.96
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Isocadinanol A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9831 98.31%
Caco-2 + 0.6453 64.53%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5071 50.71%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.9125 91.25%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8868 88.68%
P-glycoprotein inhibitior - 0.9338 93.38%
P-glycoprotein substrate - 0.7346 73.46%
CYP3A4 substrate + 0.5980 59.80%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.6705 67.05%
CYP3A4 inhibition - 0.9355 93.55%
CYP2C9 inhibition - 0.7815 78.15%
CYP2C19 inhibition - 0.7513 75.13%
CYP2D6 inhibition - 0.9447 94.47%
CYP1A2 inhibition - 0.6826 68.26%
CYP2C8 inhibition - 0.9238 92.38%
CYP inhibitory promiscuity - 0.9480 94.80%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6233 62.33%
Eye corrosion - 0.9832 98.32%
Eye irritation - 0.7303 73.03%
Skin irritation - 0.6237 62.37%
Skin corrosion - 0.8847 88.47%
Ames mutagenesis - 0.6328 63.28%
Human Ether-a-go-go-Related Gene inhibition - 0.6454 64.54%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5483 54.83%
skin sensitisation - 0.7029 70.29%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6502 65.02%
Acute Oral Toxicity (c) III 0.5665 56.65%
Estrogen receptor binding + 0.7727 77.27%
Androgen receptor binding + 0.5528 55.28%
Thyroid receptor binding + 0.6407 64.07%
Glucocorticoid receptor binding + 0.6829 68.29%
Aromatase binding - 0.5821 58.21%
PPAR gamma - 0.6894 68.94%
Honey bee toxicity - 0.7711 77.11%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity - 0.3750 37.50%

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 95.99% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.57% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 89.34% 97.79%
CHEMBL237 P41145 Kappa opioid receptor 88.89% 98.10%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.73% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 87.75% 95.93%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.06% 99.18%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.57% 91.11%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.48% 96.61%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.33% 100.00%
CHEMBL3045 P05771 Protein kinase C beta 83.89% 97.63%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.61% 95.89%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.67% 96.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.11% 95.89%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 81.15% 95.58%
CHEMBL4444 P04070 Vitamin K-dependent protein C 81.04% 93.89%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 80.16% 98.46%
CHEMBL299 P17252 Protein kinase C alpha 80.01% 98.03%

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 122211425
LOTUS LTS0002219
wikiData Q75055156