Cadala-1(10),3,8-triene

Details

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Internal ID 2d4226fc-a388-4973-9e4a-5e8461d004ca
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2,5-dimethyl-8-propan-2-yl-1,2,8,8a-tetrahydronaphthalene
SMILES (Canonical) CC1CC2C(C=CC(=C2C=C1)C)C(C)C
SMILES (Isomeric) CC1CC2C(C=CC(=C2C=C1)C)C(C)C
InChI InChI=1S/C15H22/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h5-8,10-11,13,15H,9H2,1-4H3
InChI Key GHOAKWKHPKLCNK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.36
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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GHOAKWKHPKLCNK-UHFFFAOYSA-N
8-isopropyl-2,5-dimethyl-1,2,8,8a-tetrahydro-naphthalene
8-Isopropyl-2,5-dimethyl-1,2,8,8a-tetrahydronaphthalene #

2D Structure

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2D Structure of Cadala-1(10),3,8-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.8657 86.57%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.6575 65.75%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.9458 94.58%
OATP1B3 inhibitior + 0.9380 93.80%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8078 80.78%
P-glycoprotein inhibitior - 0.9576 95.76%
P-glycoprotein substrate - 0.8636 86.36%
CYP3A4 substrate - 0.5965 59.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7535 75.35%
CYP3A4 inhibition - 0.8180 81.80%
CYP2C9 inhibition - 0.7511 75.11%
CYP2C19 inhibition - 0.7116 71.16%
CYP2D6 inhibition - 0.8331 83.31%
CYP1A2 inhibition - 0.6545 65.45%
CYP2C8 inhibition - 0.9586 95.86%
CYP inhibitory promiscuity + 0.6132 61.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Warning 0.4569 45.69%
Eye corrosion - 0.8438 84.38%
Eye irritation - 0.6634 66.34%
Skin irritation - 0.6084 60.84%
Skin corrosion - 0.9327 93.27%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7038 70.38%
Micronuclear - 0.9108 91.08%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.8739 87.39%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.7877 78.77%
Acute Oral Toxicity (c) III 0.7050 70.50%
Estrogen receptor binding - 0.8899 88.99%
Androgen receptor binding - 0.6595 65.95%
Thyroid receptor binding - 0.7873 78.73%
Glucocorticoid receptor binding - 0.8484 84.84%
Aromatase binding - 0.7953 79.53%
PPAR gamma - 0.8956 89.56%
Honey bee toxicity - 0.9389 93.89%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9912 99.12%

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 89.87% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.46% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.26% 98.95%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 86.09% 97.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.20% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.05% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.34% 85.14%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.77% 90.71%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.81% 86.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.84% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.09% 91.11%

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.
Chrysanthemum indicum

Cross-Links

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PubChem 593889
NPASS NPC225880