Caryophyllane

Details

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Internal ID ecc1a7a3-7209-4791-8206-f0ff01e44abb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2,6,10,10-tetramethylbicyclo[7.2.0]undecane
SMILES (Canonical) CC1CCCC(C2CC(C2CC1)(C)C)C
SMILES (Isomeric) CC1CCCC(C2CC(C2CC1)(C)C)C
InChI InChI=1S/C15H28/c1-11-6-5-7-12(2)13-10-15(3,4)14(13)9-8-11/h11-14H,5-10H2,1-4H3
InChI Key SITKOPDZOGHVLY-UHFFFAOYSA-N
Popularity 1,611 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28
Molecular Weight 208.38 g/mol
Exact Mass 208.219100893 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 4.89
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2,6,10,10-tetramethylbicyclo[7.2.0]undecane
20479-00-9
CHEBI:36490
DTXSID40942652
SITKOPDZOGHVLY-UHFFFAOYSA-N
Bicyclo(7.2.0)undecane, 2,6,10,10-tetramethyl-
Q27116855

2D Structure

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2D Structure of Caryophyllane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.8520 85.20%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.8228 82.28%
OATP2B1 inhibitior - 0.8450 84.50%
OATP1B1 inhibitior + 0.9275 92.75%
OATP1B3 inhibitior + 0.9757 97.57%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9058 90.58%
P-glycoprotein inhibitior - 0.9108 91.08%
P-glycoprotein substrate - 0.9357 93.57%
CYP3A4 substrate + 0.5540 55.40%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.7237 72.37%
CYP3A4 inhibition - 0.9428 94.28%
CYP2C9 inhibition - 0.8490 84.90%
CYP2C19 inhibition - 0.8792 87.92%
CYP2D6 inhibition - 0.9552 95.52%
CYP1A2 inhibition - 0.8245 82.45%
CYP2C8 inhibition - 0.9335 93.35%
CYP inhibitory promiscuity - 0.9553 95.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.5222 52.22%
Eye corrosion + 0.5505 55.05%
Eye irritation + 0.9376 93.76%
Skin irritation + 0.6331 63.31%
Skin corrosion - 0.9471 94.71%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6709 67.09%
skin sensitisation + 0.7991 79.91%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity + 0.5733 57.33%
Nephrotoxicity + 0.5917 59.17%
Acute Oral Toxicity (c) IV 0.5721 57.21%
Estrogen receptor binding - 0.7811 78.11%
Androgen receptor binding - 0.7110 71.10%
Thyroid receptor binding - 0.6004 60.04%
Glucocorticoid receptor binding - 0.7975 79.75%
Aromatase binding - 0.6608 66.08%
PPAR gamma - 0.8771 87.71%
Honey bee toxicity - 0.7556 75.56%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.8500 85.00%
Fish aquatic toxicity + 0.9789 97.89%

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 94.33% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.26% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.90% 92.94%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 88.84% 95.27%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.77% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 84.94% 99.18%
CHEMBL4040 P28482 MAP kinase ERK2 84.85% 83.82%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.29% 86.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.13% 95.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.06% 100.00%
CHEMBL206 P03372 Estrogen receptor alpha 81.72% 97.64%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.63% 93.04%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 81.60% 94.78%
CHEMBL1871 P10275 Androgen Receptor 81.37% 96.43%

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

Cross-Links

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PubChem 177131
NPASS NPC82566
LOTUS LTS0175300
wikiData Q27116855