Dehydroaromadendrene

Details

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Internal ID 04dabb46-4507-4de7-8de6-a88ad3d9ac5f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name (1aS,7S,7bR)-1,1,4,7-tetramethyl-1a,2,4a,5,6,7,7a,7b-octahydrocyclopropa[e]azulene
SMILES (Canonical) CC1CCC2C1C3C(C3(C)C)CC=C2C
SMILES (Isomeric) C[C@H]1CCC2C1[C@@H]3[C@@H](C3(C)C)CC=C2C
InChI InChI=1S/C15H24/c1-9-6-8-12-14(15(12,3)4)13-10(2)5-7-11(9)13/h6,10-14H,5,7-8H2,1-4H3/t10-,11?,12-,13?,14-/m0/s1
InChI Key DJAYTQZJAJXFDU-QKFQPQGLSA-N
Popularity 3 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 4.50
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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DJAYTQZJAJXFDU-QKFQPQGLSA-N
Q67879828

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 + 0.9917 99.17%
Caco-2 + 0.8264 82.64%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.6660 66.60%
OATP2B1 inhibitior - 0.8495 84.95%
OATP1B1 inhibitior + 0.9145 91.45%
OATP1B3 inhibitior + 0.9430 94.30%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9342 93.42%
P-glycoprotein inhibitior - 0.9249 92.49%
P-glycoprotein substrate - 0.8736 87.36%
CYP3A4 substrate + 0.5446 54.46%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.9269 92.69%
CYP2C9 inhibition - 0.7723 77.23%
CYP2C19 inhibition - 0.7297 72.97%
CYP2D6 inhibition - 0.9165 91.65%
CYP1A2 inhibition - 0.7147 71.47%
CYP2C8 inhibition - 0.6141 61.41%
CYP inhibitory promiscuity - 0.7688 76.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.4716 47.16%
Eye corrosion - 0.9114 91.14%
Eye irritation + 0.5872 58.72%
Skin irritation + 0.6741 67.41%
Skin corrosion - 0.9412 94.12%
Ames mutagenesis - 0.7870 78.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6774 67.74%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.8179 81.79%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5539 55.39%
Acute Oral Toxicity (c) III 0.8179 81.79%
Estrogen receptor binding - 0.6941 69.41%
Androgen receptor binding + 0.5209 52.09%
Thyroid receptor binding - 0.7437 74.37%
Glucocorticoid receptor binding - 0.8273 82.73%
Aromatase binding - 0.8699 86.99%
PPAR gamma - 0.7805 78.05%
Honey bee toxicity - 0.8114 81.14%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.8500 85.00%
Fish aquatic toxicity + 0.9864 98.64%

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
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 95.03% 86.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.24% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.40% 97.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.56% 94.80%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.57% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.16% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 83.89% 83.82%
CHEMBL1871 P10275 Androgen Receptor 83.23% 96.43%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.00% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.48% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.42% 93.56%

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
Hypericum rumeliacum
Phlomis lanata
Valeriana jatamansi

Cross-Links

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PubChem 91746711
NPASS NPC28402
LOTUS LTS0105234
wikiData Q67879828