3-[15-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-8,12-dimethyl-2,6-dioxahexacyclo[9.8.0.01,3.03,8.05,7.012,17]nonadecan-7-yl]-2H-furan-5-one

Details

Top
Internal ID 24f2e016-0791-4f79-80ab-e392458fb317
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Cardenolides and derivatives > Cardenolide glycosides and derivatives
IUPAC Name 3-[15-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-8,12-dimethyl-2,6-dioxahexacyclo[9.8.0.01,3.03,8.05,7.012,17]nonadecan-7-yl]-2H-furan-5-one
SMILES (Canonical) CC1C(C(CC(O1)OC2CCC3(C(C2)CCC45C3CCC6(C4(O5)CC7C6(O7)C8=CC(=O)OC8)C)C)OC)O
SMILES (Isomeric) CC1C(C(CC(O1)OC2CCC3(C(C2)CCC45C3CCC6(C4(O5)CC7C6(O7)C8=CC(=O)OC8)C)C)OC)O
InChI InChI=1S/C30H42O8/c1-16-25(32)20(33-4)13-24(35-16)36-19-6-8-26(2)17(11-19)5-10-28-21(26)7-9-27(3)29(28,38-28)14-22-30(27,37-22)18-12-23(31)34-15-18/h12,16-17,19-22,24-25,32H,5-11,13-15H2,1-4H3
InChI Key SEHQMXOXGIZASS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H42O8
Molecular Weight 530.60 g/mol
Exact Mass 530.28796829 g/mol
Topological Polar Surface Area (TPSA) 99.30 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-[15-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-8,12-dimethyl-2,6-dioxahexacyclo[9.8.0.01,3.03,8.05,7.012,17]nonadecan-7-yl]-2H-furan-5-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9851 98.51%
Caco-2 - 0.7600 76.00%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7962 79.62%
OATP2B1 inhibitior - 0.7155 71.55%
OATP1B1 inhibitior + 0.8858 88.58%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8937 89.37%
P-glycoprotein inhibitior + 0.6975 69.75%
P-glycoprotein substrate + 0.6904 69.04%
CYP3A4 substrate + 0.7342 73.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8898 88.98%
CYP3A4 inhibition - 0.7777 77.77%
CYP2C9 inhibition - 0.8098 80.98%
CYP2C19 inhibition - 0.8716 87.16%
CYP2D6 inhibition - 0.9424 94.24%
CYP1A2 inhibition - 0.8128 81.28%
CYP2C8 inhibition - 0.5720 57.20%
CYP inhibitory promiscuity - 0.9017 90.17%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6112 61.12%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.9295 92.95%
Skin irritation - 0.6647 66.47%
Skin corrosion - 0.9387 93.87%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3861 38.61%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.6519 65.19%
skin sensitisation - 0.8666 86.66%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) I 0.4639 46.39%
Estrogen receptor binding + 0.6908 69.08%
Androgen receptor binding + 0.7800 78.00%
Thyroid receptor binding - 0.5226 52.26%
Glucocorticoid receptor binding + 0.7995 79.95%
Aromatase binding + 0.7178 71.78%
PPAR gamma + 0.6361 63.61%
Honey bee toxicity - 0.6438 64.38%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9701 97.01%

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
CHEMBL226 P30542 Adenosine A1 receptor 96.74% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.96% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.79% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 93.42% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.80% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.99% 89.00%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 91.15% 94.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.36% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.91% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.52% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.40% 95.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.82% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.95% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.81% 99.23%
CHEMBL1871 P10275 Androgen Receptor 85.79% 96.43%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.14% 94.45%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 82.10% 97.33%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.32% 95.71%
CHEMBL1859 O95180 Voltage-gated T-type calcium channel alpha-1H subunit 80.98% 98.57%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.91% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.73% 82.69%
CHEMBL1937 Q92769 Histone deacetylase 2 80.12% 94.75%
CHEMBL344 Q99705 Melanin-concentrating hormone receptor 1 80.00% 92.50%

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.
Nerium oleander

Cross-Links

Top
PubChem 73323723
LOTUS LTS0220065
wikiData Q105251175