trans-beta-Guaiene

Details

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Internal ID 64713cd2-d2d6-4214-9f0b-3c42ab156886
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,4S)-1,4-dimethyl-7-propan-2-ylidene-2,3,4,5,6,8-hexahydro-1H-azulene
SMILES (Canonical) CC1CCC(=C(C)C)CC2=C1CCC2C
SMILES (Isomeric) C[C@H]1CCC(=C(C)C)CC2=C1CC[C@H]2C
InChI InChI=1S/C15H24/c1-10(2)13-7-5-11(3)14-8-6-12(4)15(14)9-13/h11-12H,5-9H2,1-4H3/t11-,12+/m0/s1
InChI Key GIBQERSGRNPMEH-NWDGAFQWSA-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 4.10
Atomic LogP (AlogP) 4.87
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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DTXSID801037462
1,2,3,4,5,6,7,8-Octahydro-1alpha,4beta-dimethyl-7-(1-methylethylidene)azulene
192053-49-9

2D Structure

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2D Structure of trans-beta-Guaiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.9461 94.61%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.5690 56.90%
OATP2B1 inhibitior - 0.8442 84.42%
OATP1B1 inhibitior + 0.9427 94.27%
OATP1B3 inhibitior + 0.9656 96.56%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8232 82.32%
P-glycoprotein inhibitior - 0.8830 88.30%
P-glycoprotein substrate - 0.9557 95.57%
CYP3A4 substrate - 0.5972 59.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7217 72.17%
CYP3A4 inhibition - 0.9636 96.36%
CYP2C9 inhibition - 0.7633 76.33%
CYP2C19 inhibition - 0.7642 76.42%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.6394 63.94%
CYP2C8 inhibition - 0.9351 93.51%
CYP inhibitory promiscuity - 0.7706 77.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.4614 46.14%
Eye corrosion - 0.8353 83.53%
Eye irritation + 0.9090 90.90%
Skin irritation + 0.5993 59.93%
Skin corrosion - 0.9622 96.22%
Ames mutagenesis - 0.8854 88.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7209 72.09%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.8446 84.46%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6636 66.36%
Acute Oral Toxicity (c) III 0.8364 83.64%
Estrogen receptor binding - 0.9279 92.79%
Androgen receptor binding - 0.6344 63.44%
Thyroid receptor binding - 0.6779 67.79%
Glucocorticoid receptor binding - 0.8451 84.51%
Aromatase binding - 0.8937 89.37%
PPAR gamma - 0.8584 85.84%
Honey bee toxicity - 0.9351 93.51%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9959 99.59%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.83% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.78% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.63% 92.94%

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.
Atractylodes lancea
Pogostemon cablin

Cross-Links

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PubChem 92173696
NPASS NPC203699