Cycloisolongifolene

Details

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Internal ID a72d73de-ca1a-4459-8cec-3cc81b112e13
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 2,2,7,7-tetramethyltetracyclo[6.2.1.01,6.06,10]undecane
SMILES (Canonical) CC1(CCCC23C14C2CC(C4)C3(C)C)C
SMILES (Isomeric) CC1(CCCC23C14C2CC(C4)C3(C)C)C
InChI InChI=1S/C15H24/c1-12(2)6-5-7-14-11-8-10(13(14,3)4)9-15(11,12)14/h10-11H,5-9H2,1-4H3
InChI Key VRSGYUIZSVSWIY-UHFFFAOYSA-N
Popularity 1 reference 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 5.20
Atomic LogP (AlogP) 4.25
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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VRSGYUIZSVSWIY-UHFFFAOYSA-N

2D Structure

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2D Structure of Cycloisolongifolene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.8427 84.27%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.7826 78.26%
OATP2B1 inhibitior - 0.8462 84.62%
OATP1B1 inhibitior + 0.9483 94.83%
OATP1B3 inhibitior + 0.9620 96.20%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9626 96.26%
P-glycoprotein inhibitior - 0.9428 94.28%
P-glycoprotein substrate - 0.8633 86.33%
CYP3A4 substrate + 0.5290 52.90%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.7359 73.59%
CYP3A4 inhibition - 0.9191 91.91%
CYP2C9 inhibition - 0.7780 77.80%
CYP2C19 inhibition - 0.7803 78.03%
CYP2D6 inhibition - 0.9417 94.17%
CYP1A2 inhibition - 0.8312 83.12%
CYP2C8 inhibition - 0.9427 94.27%
CYP inhibitory promiscuity - 0.8112 81.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.5306 53.06%
Eye corrosion - 0.8779 87.79%
Eye irritation + 0.9359 93.59%
Skin irritation - 0.5916 59.16%
Skin corrosion - 0.9339 93.39%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5406 54.06%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6074 60.74%
skin sensitisation + 0.6850 68.50%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5669 56.69%
Acute Oral Toxicity (c) III 0.5660 56.60%
Estrogen receptor binding - 0.7382 73.82%
Androgen receptor binding + 0.6305 63.05%
Thyroid receptor binding - 0.7131 71.31%
Glucocorticoid receptor binding - 0.7949 79.49%
Aromatase binding - 0.5218 52.18%
PPAR gamma - 0.7709 77.09%
Honey bee toxicity - 0.7496 74.96%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9953 99.53%

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 96.53% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 95.75% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.45% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 88.20% 94.75%
CHEMBL259 P32245 Melanocortin receptor 4 86.86% 95.38%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 85.72% 95.27%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.62% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.85% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 84.75% 95.93%
CHEMBL238 Q01959 Dopamine transporter 84.19% 95.88%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.38% 95.89%

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.
Curcuma longa
Gossypium herbaceum

Cross-Links

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PubChem 563197
NPASS NPC126396