Cadina-4,9-diene

Details

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Internal ID a3b4e8d8-7625-4ce1-acd6-200e7aeae8a9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (5R)-3,8-dimethyl-5-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene
SMILES (Canonical) CC1CCC2C(=CCC(C2=C1)C(C)C)C
SMILES (Isomeric) CC1CCC2C(=CC[C@@H](C2=C1)C(C)C)C
InChI InChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h6,9-11,13-14H,5,7-8H2,1-4H3/t11?,13-,14?/m1/s1
InChI Key VIJZUYWOPTZBJY-HRDQMINSSA-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 4.30
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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VIJZUYWOPTZBJY-HRDQMINSSA-N

2D Structure

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2D Structure of Cadina-4,9-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.9224 92.24%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.5757 57.57%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9454 94.54%
OATP1B3 inhibitior + 0.9077 90.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8755 87.55%
P-glycoprotein inhibitior - 0.9498 94.98%
P-glycoprotein substrate - 0.7853 78.53%
CYP3A4 substrate - 0.5774 57.74%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.6973 69.73%
CYP3A4 inhibition - 0.9533 95.33%
CYP2C9 inhibition - 0.7784 77.84%
CYP2C19 inhibition - 0.7003 70.03%
CYP2D6 inhibition - 0.9012 90.12%
CYP1A2 inhibition - 0.7367 73.67%
CYP2C8 inhibition - 0.9404 94.04%
CYP inhibitory promiscuity - 0.5930 59.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.4516 45.16%
Eye corrosion - 0.8932 89.32%
Eye irritation - 0.7210 72.10%
Skin irritation - 0.5805 58.05%
Skin corrosion - 0.8924 89.24%
Ames mutagenesis - 0.7037 70.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4710 47.10%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.8745 87.45%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.7242 72.42%
Acute Oral Toxicity (c) III 0.7008 70.08%
Estrogen receptor binding - 0.9384 93.84%
Androgen receptor binding - 0.8507 85.07%
Thyroid receptor binding - 0.7890 78.90%
Glucocorticoid receptor binding - 0.7247 72.47%
Aromatase binding - 0.9370 93.70%
PPAR gamma - 0.8440 84.40%
Honey bee toxicity - 0.8927 89.27%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9963 99.63%

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
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 89.45% 86.00%
CHEMBL2581 P07339 Cathepsin D 88.55% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.34% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.74% 93.56%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 85.98% 97.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.96% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.44% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.62% 99.18%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.41% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.18% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.85% 95.89%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.14% 96.47%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.12% 90.24%

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.
Agastache rugosa
Magnolia biondii
Magnolia denudata
Magnolia kobus
Magnolia salicifolia
Magnolia sprengeri
Schisandra chinensis

Cross-Links

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PubChem 91748288
NPASS NPC19460