beta-Ylangene

Details

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Internal ID 25c9c958-4cb5-4c57-8bd4-aa087276ceff
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-methyl-3-methylidene-8-propan-2-yltricyclo[4.4.0.02,7]decane
SMILES (Canonical) CC(C)C1CCC2(C3C1C2C(=C)CC3)C
SMILES (Isomeric) CC(C)C1CCC2(C3C1C2C(=C)CC3)C
InChI InChI=1S/C15H24/c1-9(2)11-7-8-15(4)12-6-5-10(3)14(15)13(11)12/h9,11-14H,3,5-8H2,1-2,4H3
InChI Key UPVZPMJSRSWJHQ-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 4.70
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Tricyclo[4.4.0.0(2,7)]decane, 1-methyl-3-methylene-8-(1-methylethyl)-, stereoisomer
UPVZPMJSRSWJHQ-UHFFFAOYSA-N
Tricyclo[4.4.0.0(2,7)]decane, 8-isopropyl-1-methyl-3-methylene-, syn-8-

2D Structure

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2D Structure of beta-Ylangene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.8217 82.17%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.6843 68.43%
OATP2B1 inhibitior - 0.8498 84.98%
OATP1B1 inhibitior + 0.9319 93.19%
OATP1B3 inhibitior + 0.8874 88.74%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9012 90.12%
P-glycoprotein inhibitior - 0.8879 88.79%
P-glycoprotein substrate - 0.8813 88.13%
CYP3A4 substrate + 0.5642 56.42%
CYP2C9 substrate - 0.7731 77.31%
CYP2D6 substrate - 0.7252 72.52%
CYP3A4 inhibition - 0.7969 79.69%
CYP2C9 inhibition - 0.6098 60.98%
CYP2C19 inhibition + 0.5051 50.51%
CYP2D6 inhibition - 0.9186 91.86%
CYP1A2 inhibition - 0.7789 77.89%
CYP2C8 inhibition - 0.8389 83.89%
CYP inhibitory promiscuity - 0.6627 66.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.4568 45.68%
Eye corrosion - 0.9304 93.04%
Eye irritation + 0.8128 81.28%
Skin irritation - 0.5799 57.99%
Skin corrosion - 0.9573 95.73%
Ames mutagenesis - 0.8423 84.23%
Human Ether-a-go-go-Related Gene inhibition - 0.5669 56.69%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6847 68.47%
skin sensitisation + 0.7838 78.38%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6472 64.72%
Acute Oral Toxicity (c) III 0.8384 83.84%
Estrogen receptor binding - 0.7153 71.53%
Androgen receptor binding + 0.6859 68.59%
Thyroid receptor binding - 0.6366 63.66%
Glucocorticoid receptor binding - 0.6147 61.47%
Aromatase binding - 0.8265 82.65%
PPAR gamma - 0.8030 80.30%
Honey bee toxicity - 0.8684 86.84%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 1.0000 100.00%

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 96.72% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 93.11% 94.75%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 92.66% 85.30%
CHEMBL221 P23219 Cyclooxygenase-1 91.12% 90.17%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.06% 96.38%
CHEMBL2996 Q05655 Protein kinase C delta 87.73% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.71% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.49% 91.11%
CHEMBL3524 P56524 Histone deacetylase 4 86.30% 92.97%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.59% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.00% 96.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.65% 93.04%
CHEMBL1871 P10275 Androgen Receptor 82.24% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.40% 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.
Capsicum annuum
Hypericum perforatum
Schisandra chinensis

Cross-Links

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PubChem 519779
NPASS NPC252268