(1S,3R,5R,6S,7S,9R,10R,13R,14S,16S,19R,21S,23S,24R,25R)-7,13,14,16,24,25-hexahydroxy-1-methoxy-5,9,23-trimethyl-10-(6-oxopyran-3-yl)-2,20,22-trioxahexacyclo[19.3.1.03,19.05,17.06,14.09,13]pentacos-17-en-8-one

Details

Top
Internal ID adf9b519-48e4-4f88-898f-7de90f03f420
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Bufanolides and derivatives
IUPAC Name (1S,3R,5R,6S,7S,9R,10R,13R,14S,16S,19R,21S,23S,24R,25R)-7,13,14,16,24,25-hexahydroxy-1-methoxy-5,9,23-trimethyl-10-(6-oxopyran-3-yl)-2,20,22-trioxahexacyclo[19.3.1.03,19.05,17.06,14.09,13]pentacos-17-en-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H40O13/c1-13-23(35)31(40-4)25(37)26(42-13)43-18-9-16-17(32)10-29(38)22(27(16,2)11-19(18)44-31)21(34)24(36)28(3)15(7-8-30(28,29)39)14-5-6-20(33)41-12-14/h5-6,9,12-13,15,17-19,21-23,25-26,32,34-35,37-39H,7-8,10-11H2,1-4H3/t13-,15+,17-,18+,19+,21-,22+,23+,25+,26-,27-,28-,29-,30+,31-/m0/s1
InChI Key MWBWDSBAVQXNEL-BJMTXSORSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C31H40O13
Molecular Weight 620.60 g/mol
Exact Mass 620.24689133 g/mol
Topological Polar Surface Area (TPSA) 202.00 Ų
XlogP -2.60
Atomic LogP (AlogP) -0.76
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (1S,3R,5R,6S,7S,9R,10R,13R,14S,16S,19R,21S,23S,24R,25R)-7,13,14,16,24,25-hexahydroxy-1-methoxy-5,9,23-trimethyl-10-(6-oxopyran-3-yl)-2,20,22-trioxahexacyclo[19.3.1.03,19.05,17.06,14.09,13]pentacos-17-en-8-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9472 94.72%
Caco-2 - 0.8508 85.08%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6921 69.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8465 84.65%
OATP1B3 inhibitior + 0.9170 91.70%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9321 93.21%
BSEP inhibitior + 0.5931 59.31%
P-glycoprotein inhibitior + 0.6360 63.60%
P-glycoprotein substrate + 0.6317 63.17%
CYP3A4 substrate + 0.7131 71.31%
CYP2C9 substrate - 0.7976 79.76%
CYP2D6 substrate - 0.8729 87.29%
CYP3A4 inhibition - 0.7700 77.00%
CYP2C9 inhibition - 0.8230 82.30%
CYP2C19 inhibition - 0.8334 83.34%
CYP2D6 inhibition - 0.9270 92.70%
CYP1A2 inhibition - 0.8516 85.16%
CYP2C8 inhibition + 0.6503 65.03%
CYP inhibitory promiscuity - 0.9326 93.26%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5347 53.47%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9273 92.73%
Skin irritation - 0.6187 61.87%
Skin corrosion - 0.9240 92.40%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6298 62.98%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8672 86.72%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.7217 72.17%
Acute Oral Toxicity (c) II 0.6736 67.36%
Estrogen receptor binding + 0.8123 81.23%
Androgen receptor binding + 0.7523 75.23%
Thyroid receptor binding + 0.5547 55.47%
Glucocorticoid receptor binding + 0.7070 70.70%
Aromatase binding + 0.6899 68.99%
PPAR gamma + 0.6826 68.26%
Honey bee toxicity - 0.7172 71.72%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9916 99.16%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.25% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.56% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.83% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.45% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.68% 97.09%
CHEMBL4208 P20618 Proteasome component C5 91.20% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.44% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.78% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.16% 89.00%
CHEMBL2581 P07339 Cathepsin D 88.62% 98.95%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.21% 97.36%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.69% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.64% 95.89%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.70% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.16% 100.00%
CHEMBL332 P03956 Matrix metalloproteinase-1 83.18% 94.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.03% 93.99%

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.
Drimia macrocentra

Cross-Links

Top
PubChem 162931826
LOTUS LTS0029515
wikiData Q105173498