(-)-Dehydroaromadendrene

Details

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Internal ID c0bec348-5916-415d-b0b9-77b53d50d289
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Aromadendrane sesquiterpenoids > 5,10-cycloaromadendrane sesquiterpenoids
IUPAC Name 1,1,7-trimethyl-4-methylidene-4a,5,6,7,7a,7b-hexahydro-1aH-cyclopropa[e]azulene
SMILES (Canonical) CC1CCC2C1C3C(C3(C)C)C=CC2=C
SMILES (Isomeric) CC1CCC2C1C3C(C3(C)C)C=CC2=C
InChI InChI=1S/C15H22/c1-9-6-8-12-14(15(12,3)4)13-10(2)5-7-11(9)13/h6,8,10-14H,1,5,7H2,2-4H3
InChI Key OXBYVYGWWRTWMD-UHFFFAOYSA-N
Popularity 0 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 4.50
Atomic LogP (AlogP) 4.05
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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OXBYVYGWWRTWMD-UHFFFAOYSA-N

2D Structure

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2D Structure of (-)-Dehydroaromadendrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.7863 78.63%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.6390 63.90%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.9000 90.00%
OATP1B3 inhibitior + 0.9296 92.96%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9758 97.58%
P-glycoprotein inhibitior - 0.9240 92.40%
P-glycoprotein substrate - 0.8430 84.30%
CYP3A4 substrate + 0.5163 51.63%
CYP2C9 substrate - 0.8117 81.17%
CYP2D6 substrate - 0.7885 78.85%
CYP3A4 inhibition - 0.8743 87.43%
CYP2C9 inhibition - 0.7619 76.19%
CYP2C19 inhibition - 0.6820 68.20%
CYP2D6 inhibition - 0.9011 90.11%
CYP1A2 inhibition - 0.6563 65.63%
CYP2C8 inhibition - 0.7395 73.95%
CYP inhibitory promiscuity - 0.7641 76.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.4585 45.85%
Eye corrosion - 0.8920 89.20%
Eye irritation - 0.6302 63.02%
Skin irritation + 0.6477 64.77%
Skin corrosion - 0.9447 94.47%
Ames mutagenesis - 0.8170 81.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7223 72.23%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation + 0.7978 79.78%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.5215 52.15%
Nephrotoxicity + 0.5248 52.48%
Acute Oral Toxicity (c) III 0.8189 81.89%
Estrogen receptor binding - 0.5628 56.28%
Androgen receptor binding + 0.5501 55.01%
Thyroid receptor binding - 0.6847 68.47%
Glucocorticoid receptor binding - 0.7384 73.84%
Aromatase binding - 0.8138 81.38%
PPAR gamma - 0.8154 81.54%
Honey bee toxicity - 0.8465 84.65%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity + 0.9866 98.66%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.01% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.87% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 91.64% 86.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.47% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.05% 97.25%
CHEMBL2581 P07339 Cathepsin D 87.69% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.55% 94.80%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.12% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.56% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.74% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.60% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.84% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.59% 86.33%

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.
Atractylodes lancea
Atractylodes macrocephala
Valeriana jatamansi

Cross-Links

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PubChem 526687
NPASS NPC309317