(4S)-4-Methoxycepharosporolide C

Details

Top
Internal ID fc64bc76-361c-43b3-8345-1139dbbaf039
Taxonomy Organoheterocyclic compounds > Lactones
IUPAC Name (4S,5S,10R)-4-hydroxy-5-methoxy-10-methyloxecane-2,7-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H18O5/c1-7-3-4-8(12)5-10(15-2)9(13)6-11(14)16-7/h7,9-10,13H,3-6H2,1-2H3/t7-,9+,10+/m1/s1
InChI Key RKWVKFFFOYCNSI-JEZHCXPESA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H18O5
Molecular Weight 230.26 g/mol
Exact Mass 230.11542367 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP -0.40
Atomic LogP (AlogP) 0.44
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (4S)-4-Methoxycepharosporolide C

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9524 95.24%
Caco-2 + 0.7332 73.32%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7577 75.77%
OATP2B1 inhibitior - 0.8463 84.63%
OATP1B1 inhibitior + 0.9370 93.70%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9156 91.56%
P-glycoprotein inhibitior - 0.9033 90.33%
P-glycoprotein substrate - 0.8696 86.96%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8446 84.46%
CYP3A4 inhibition - 0.8140 81.40%
CYP2C9 inhibition - 0.9492 94.92%
CYP2C19 inhibition - 0.9004 90.04%
CYP2D6 inhibition - 0.9605 96.05%
CYP1A2 inhibition - 0.7255 72.55%
CYP2C8 inhibition - 0.9545 95.45%
CYP inhibitory promiscuity - 0.9949 99.49%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.7505 75.05%
Eye corrosion - 0.9446 94.46%
Eye irritation - 0.5285 52.85%
Skin irritation - 0.6649 66.49%
Skin corrosion - 0.9214 92.14%
Ames mutagenesis - 0.5908 59.08%
Human Ether-a-go-go-Related Gene inhibition - 0.5746 57.46%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.6730 67.30%
skin sensitisation - 0.9059 90.59%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5798 57.98%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.4621 46.21%
Acute Oral Toxicity (c) III 0.4918 49.18%
Estrogen receptor binding - 0.8174 81.74%
Androgen receptor binding - 0.7764 77.64%
Thyroid receptor binding - 0.7875 78.75%
Glucocorticoid receptor binding - 0.7506 75.06%
Aromatase binding - 0.9403 94.03%
PPAR gamma - 0.7618 76.18%
Honey bee toxicity - 0.9064 90.64%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.7735 77.35%

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 91.30% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.47% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.16% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.69% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.46% 92.94%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.42% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.23% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.90% 99.23%
CHEMBL1902 P62942 FK506-binding protein 1A 82.81% 97.05%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.71% 95.89%

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.
There are no matching plants.

Cross-Links

Top
PubChem 11310764
LOTUS LTS0031574
wikiData Q105239563