(+)-beta-Amorphene

Details

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Internal ID 74c542aa-854a-488f-8687-9878016ce6b1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,4aR,8aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,8,8a-hexahydronaphthalene
SMILES (Canonical) CC1=CCC2C(C1)C(CC=C2C)C(C)C
SMILES (Isomeric) CC1=CC[C@@H]2[C@H](C1)[C@@H](CC=C2C)C(C)C
InChI InChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h5-6,10,13-15H,7-9H2,1-4H3/t13-,14-,15+/m0/s1
InChI Key USDOQCCMRDNVAH-SOUVJXGZSA-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 4.00
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (+)-beta-Amorphene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.8891 88.91%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.6507 65.07%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9566 95.66%
OATP1B3 inhibitior + 0.9349 93.49%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8847 88.47%
P-glycoprotein inhibitior - 0.9625 96.25%
P-glycoprotein substrate - 0.8126 81.26%
CYP3A4 substrate - 0.5885 58.85%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.6973 69.73%
CYP3A4 inhibition - 0.8454 84.54%
CYP2C9 inhibition - 0.7576 75.76%
CYP2C19 inhibition - 0.6915 69.15%
CYP2D6 inhibition - 0.8908 89.08%
CYP1A2 inhibition - 0.7087 70.87%
CYP2C8 inhibition - 0.9171 91.71%
CYP inhibitory promiscuity - 0.5095 50.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.4445 44.45%
Eye corrosion - 0.8655 86.55%
Eye irritation + 0.5465 54.65%
Skin irritation - 0.5477 54.77%
Skin corrosion - 0.9263 92.63%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3808 38.08%
Micronuclear - 0.9367 93.67%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.8565 85.65%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.5571 55.71%
Acute Oral Toxicity (c) III 0.6727 67.27%
Estrogen receptor binding - 0.9444 94.44%
Androgen receptor binding - 0.6355 63.55%
Thyroid receptor binding - 0.8547 85.47%
Glucocorticoid receptor binding - 0.8594 85.94%
Aromatase binding - 0.8753 87.53%
PPAR gamma - 0.8007 80.07%
Honey bee toxicity - 0.8568 85.68%
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 90.92% 97.25%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 88.07% 86.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.97% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.75% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.72% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.90% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.33% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 82.02% 97.79%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 80.18% 90.71%

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.
Acorus gramineus
Baccharis sagittalis
Solidago canadensis

Cross-Links

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PubChem 25202382
LOTUS LTS0052995
wikiData Q105278159