Butyrospermone

Details

Top
Internal ID aa4ef067-c46f-487a-a046-292a73c03ff6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 4,4,10,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
SMILES (Canonical) CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C
SMILES (Isomeric) CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C
InChI InChI=1S/C30H48O/c1-20(2)10-9-11-21(3)22-14-18-30(8)24-12-13-25-27(4,5)26(31)16-17-28(25,6)23(24)15-19-29(22,30)7/h10,12,21-23,25H,9,11,13-19H2,1-8H3
InChI Key QQWIMVRGPKFDGM-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H48O
Molecular Weight 424.70 g/mol
Exact Mass 424.370516150 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 8.90
Atomic LogP (AlogP) 8.54
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
Eupha-7,24-dien-3-one

2D Structure

Top
2D Structure of Butyrospermone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6828 68.28%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5591 55.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8528 85.28%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9607 96.07%
P-glycoprotein inhibitior + 0.7013 70.13%
P-glycoprotein substrate - 0.6958 69.58%
CYP3A4 substrate + 0.6299 62.99%
CYP2C9 substrate - 0.8039 80.39%
CYP2D6 substrate - 0.7758 77.58%
CYP3A4 inhibition - 0.8867 88.67%
CYP2C9 inhibition - 0.8897 88.97%
CYP2C19 inhibition - 0.7062 70.62%
CYP2D6 inhibition - 0.9594 95.94%
CYP1A2 inhibition - 0.8927 89.27%
CYP2C8 inhibition - 0.7407 74.07%
CYP inhibitory promiscuity - 0.6104 61.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5158 51.58%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.9477 94.77%
Skin irritation + 0.6133 61.33%
Skin corrosion - 0.9711 97.11%
Ames mutagenesis - 0.6754 67.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6991 69.91%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6572 65.72%
skin sensitisation + 0.8120 81.20%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.6413 64.13%
Acute Oral Toxicity (c) III 0.7698 76.98%
Estrogen receptor binding + 0.7994 79.94%
Androgen receptor binding + 0.7541 75.41%
Thyroid receptor binding + 0.8114 81.14%
Glucocorticoid receptor binding + 0.8719 87.19%
Aromatase binding + 0.6426 64.26%
PPAR gamma + 0.6979 69.79%
Honey bee toxicity - 0.8309 83.09%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9926 99.26%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.48% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.29% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.55% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 92.47% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.85% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.51% 90.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.16% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.98% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.33% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.95% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.75% 82.69%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.41% 93.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.11% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.22% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 82.16% 90.17%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 81.59% 94.78%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.46% 85.30%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.88% 92.62%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 80.72% 98.33%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.63% 97.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.17% 99.23%

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.
Cassia javanica
Simarouba amara

Cross-Links

Top
PubChem 4205159
LOTUS LTS0031859
wikiData Q104196110