beta-Amyrene

Details

Top
Internal ID 664eab47-d8db-4158-a3cf-adc034c5291a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene
SMILES (Canonical) CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCCC5(C)C)C)C)C2C1)C)C)C
SMILES (Isomeric) CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCCC5(C)C)C)C)C2C1)C)C)C
InChI InChI=1S/C30H50/c1-25(2)16-17-27(5)18-19-29(7)21(22(27)20-25)10-11-24-28(6)14-9-13-26(3,4)23(28)12-15-30(24,29)8/h10,22-24H,9,11-20H2,1-8H3
InChI Key ZTLIRKGRXLVPOF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H50
Molecular Weight 410.70 g/mol
Exact Mass 410.391251595 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 10.70
Atomic LogP (AlogP) 9.20
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
18beta(H)-OLEAN-12(13)-ENE
ZTLIRKGRXLVPOF-UHFFFAOYSA-N

2D Structure

Top
2D Structure of beta-Amyrene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.6886 68.86%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.6465 64.65%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.8881 88.81%
OATP1B3 inhibitior + 0.8746 87.46%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.8428 84.28%
P-glycoprotein inhibitior - 0.7145 71.45%
P-glycoprotein substrate - 0.8982 89.82%
CYP3A4 substrate + 0.5996 59.96%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.8710 87.10%
CYP2C9 inhibition - 0.7317 73.17%
CYP2C19 inhibition - 0.6019 60.19%
CYP2D6 inhibition - 0.9375 93.75%
CYP1A2 inhibition - 0.8422 84.22%
CYP2C8 inhibition - 0.5704 57.04%
CYP inhibitory promiscuity - 0.5141 51.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.4857 48.57%
Eye corrosion - 0.9650 96.50%
Eye irritation - 0.8643 86.43%
Skin irritation - 0.6920 69.20%
Skin corrosion - 0.9619 96.19%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6994 69.94%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.7466 74.66%
skin sensitisation + 0.8341 83.41%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.4619 46.19%
Acute Oral Toxicity (c) III 0.6528 65.28%
Estrogen receptor binding + 0.8200 82.00%
Androgen receptor binding + 0.6405 64.05%
Thyroid receptor binding + 0.6846 68.46%
Glucocorticoid receptor binding + 0.8313 83.13%
Aromatase binding + 0.6933 69.33%
PPAR gamma + 0.5813 58.13%
Honey bee toxicity - 0.8889 88.89%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

Top

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 95.90% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.44% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.01% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.83% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.84% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.04% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.75% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.72% 93.99%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 85.42% 94.78%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.19% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.60% 92.94%
CHEMBL2581 P07339 Cathepsin D 83.60% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 81.93% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.82% 95.56%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.03% 99.18%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.95% 96.77%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.92% 95.17%
CHEMBL259 P32245 Melanocortin receptor 4 80.08% 95.38%

Plants that contains it

Top
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.
Gymnosporia emarginata

Cross-Links

Top
PubChem 612780
LOTUS LTS0001696
wikiData Q105383005