Di-epi-alpha-cedrene-(I)

Details

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Internal ID c90b2eda-7515-4dd2-91b2-63df7b8b29af
Taxonomy Hydrocarbons > Polycyclic hydrocarbons
IUPAC Name 2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-9-ene
SMILES (Canonical) CC1CCC2C13CC(C2(C)C)C(C=C3)C
SMILES (Isomeric) CC1CCC2C13CC(C2(C)C)C(C=C3)C
InChI InChI=1S/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h7-8,10-13H,5-6,9H2,1-4H3
InChI Key KANBSDYNZJCGLT-UHFFFAOYSA-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 5.20
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Di-epi-.alpha.-cedrene-(I)
KANBSDYNZJCGLT-UHFFFAOYSA-N

2D Structure

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2D Structure of Di-epi-alpha-cedrene-(I)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.8125 81.25%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.7652 76.52%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9335 93.35%
OATP1B3 inhibitior + 0.9579 95.79%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9553 95.53%
P-glycoprotein inhibitior - 0.9271 92.71%
P-glycoprotein substrate - 0.8570 85.70%
CYP3A4 substrate + 0.5355 53.55%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.7660 76.60%
CYP3A4 inhibition - 0.9344 93.44%
CYP2C9 inhibition - 0.8449 84.49%
CYP2C19 inhibition - 0.8380 83.80%
CYP2D6 inhibition - 0.9488 94.88%
CYP1A2 inhibition - 0.8141 81.41%
CYP2C8 inhibition - 0.8617 86.17%
CYP inhibitory promiscuity - 0.8474 84.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.5241 52.41%
Eye corrosion - 0.8107 81.07%
Eye irritation - 0.5202 52.02%
Skin irritation + 0.5918 59.18%
Skin corrosion - 0.9706 97.06%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.8521 85.21%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7545 75.45%
Acute Oral Toxicity (c) III 0.6648 66.48%
Estrogen receptor binding - 0.7273 72.73%
Androgen receptor binding - 0.6579 65.79%
Thyroid receptor binding - 0.6589 65.89%
Glucocorticoid receptor binding - 0.7649 76.49%
Aromatase binding - 0.8052 80.52%
PPAR gamma - 0.7788 77.88%
Honey bee toxicity - 0.7716 77.16%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.7700 77.00%
Fish aquatic toxicity + 0.9962 99.62%

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 94.55% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.27% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.73% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.50% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.51% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.24% 100.00%
CHEMBL259 P32245 Melanocortin receptor 4 82.28% 95.38%
CHEMBL221 P23219 Cyclooxygenase-1 81.61% 90.17%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.35% 85.30%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.02% 97.14%

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.
Platycladus orientalis

Cross-Links

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PubChem 576610
NPASS NPC176943