(+)-Trans-4(11),8-aucadiene

Details

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Internal ID a874293d-c5a9-47e0-9185-4edf3788abb7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3aR,8aR)-6,8a-dimethyl-3-propan-2-ylidene-1,2,3a,4,5,8-hexahydroazulene
SMILES (Canonical) CC1=CCC2(CCC(=C(C)C)C2CC1)C
SMILES (Isomeric) CC1=CC[C@]2(CCC(=C(C)C)[C@@H]2CC1)C
InChI InChI=1S/C15H24/c1-11(2)13-8-10-15(4)9-7-12(3)5-6-14(13)15/h7,14H,5-6,8-10H2,1-4H3/t14-,15-/m0/s1
InChI Key PRQLWQYYMJZORK-GJZGRUSLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.87
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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LMPR0103550002

2D Structure

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2D Structure of (+)-Trans-4(11),8-aucadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.9210 92.10%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.6838 68.38%
OATP2B1 inhibitior - 0.8400 84.00%
OATP1B1 inhibitior + 0.9059 90.59%
OATP1B3 inhibitior + 0.9603 96.03%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7880 78.80%
P-glycoprotein inhibitior - 0.9330 93.30%
P-glycoprotein substrate - 0.8978 89.78%
CYP3A4 substrate + 0.5489 54.89%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.9194 91.94%
CYP2C9 inhibition - 0.7654 76.54%
CYP2C19 inhibition - 0.7513 75.13%
CYP2D6 inhibition - 0.9303 93.03%
CYP1A2 inhibition - 0.7572 75.72%
CYP2C8 inhibition - 0.8523 85.23%
CYP inhibitory promiscuity - 0.7869 78.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.4676 46.76%
Eye corrosion - 0.8942 89.42%
Eye irritation + 0.7819 78.19%
Skin irritation + 0.6450 64.50%
Skin corrosion - 0.9699 96.99%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7575 75.75%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5365 53.65%
skin sensitisation + 0.8457 84.57%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.5934 59.34%
Acute Oral Toxicity (c) III 0.8120 81.20%
Estrogen receptor binding - 0.9422 94.22%
Androgen receptor binding - 0.5283 52.83%
Thyroid receptor binding - 0.8100 81.00%
Glucocorticoid receptor binding - 0.7895 78.95%
Aromatase binding - 0.7039 70.39%
PPAR gamma - 0.7978 79.78%
Honey bee toxicity - 0.9425 94.25%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9952 99.52%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.24% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.29% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.23% 92.94%
CHEMBL2581 P07339 Cathepsin D 84.96% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.83% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.26% 100.00%

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.
Bazzania trilobata

Cross-Links

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PubChem 11586486
LOTUS LTS0093659
wikiData Q105213871