(+)-Isokaurene

Details

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Internal ID 9fb92ec2-21c1-4f2b-a7bb-8649c61a2d13
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name (1S,4S,9S,10R,13R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene
SMILES (Canonical) CC1=CC23CCC4C(CCCC4(C2CCC1C3)C)(C)C
SMILES (Isomeric) CC1=C[C@@]23CC[C@@H]4[C@@]([C@H]2CC[C@@H]1C3)(CCCC4(C)C)C
InChI InChI=1S/C20H32/c1-14-12-20-11-8-16-18(2,3)9-5-10-19(16,4)17(20)7-6-15(14)13-20/h12,15-17H,5-11,13H2,1-4H3/t15-,16+,17-,19+,20-/m1/s1
InChI Key DQUHDYWUEKWRLN-FPPGBKCQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32
Molecular Weight 272.50 g/mol
Exact Mass 272.250401021 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.90
Atomic LogP (AlogP) 5.98
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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511-85-3

2D Structure

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2D Structure of (+)-Isokaurene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.8029 80.29%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.6870 68.70%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.9143 91.43%
OATP1B3 inhibitior + 0.9231 92.31%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.5336 53.36%
P-glycoprotein inhibitior - 0.8218 82.18%
P-glycoprotein substrate - 0.8521 85.21%
CYP3A4 substrate + 0.5595 55.95%
CYP2C9 substrate - 0.6027 60.27%
CYP2D6 substrate - 0.7518 75.18%
CYP3A4 inhibition - 0.8704 87.04%
CYP2C9 inhibition - 0.7351 73.51%
CYP2C19 inhibition - 0.6352 63.52%
CYP2D6 inhibition - 0.9189 91.89%
CYP1A2 inhibition - 0.8346 83.46%
CYP2C8 inhibition - 0.6241 62.41%
CYP inhibitory promiscuity - 0.5843 58.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.4789 47.89%
Eye corrosion - 0.9552 95.52%
Eye irritation - 0.8534 85.34%
Skin irritation - 0.5762 57.62%
Skin corrosion - 0.9566 95.66%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3632 36.32%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.8147 81.47%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6894 68.94%
Acute Oral Toxicity (c) III 0.7965 79.65%
Estrogen receptor binding + 0.7011 70.11%
Androgen receptor binding - 0.6279 62.79%
Thyroid receptor binding + 0.6620 66.20%
Glucocorticoid receptor binding + 0.6640 66.40%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.6253 62.53%
Honey bee toxicity - 0.8659 86.59%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.01% 97.25%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.34% 96.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.10% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.42% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.74% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 85.43% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.21% 95.89%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.55% 86.00%
CHEMBL259 P32245 Melanocortin receptor 4 84.24% 95.38%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.67% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.95% 94.45%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.56% 95.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.79% 92.94%

Cross-Links

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PubChem 101297738
NPASS NPC36238
LOTUS LTS0085246
wikiData Q104987152