14,23-Dihydroxy-9-(hydroxymethyl)-9,18,23,25-tetramethyl-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacosane-5,19,24,26-tetrone

Details

Top
Internal ID 62adda1d-b0e3-45c5-a1dc-9dafc77a5b1e
Taxonomy Organoheterocyclic compounds > Furopyrans
IUPAC Name 14,23-dihydroxy-9-(hydroxymethyl)-9,18,23,25-tetramethyl-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacosane-5,19,24,26-tetrone
SMILES (Canonical) CC1C2C(C3C4C(C(=O)CC56CC78C(CCC5C(C4(O2)O6)O)C(OC7CC(=O)O8)(C)CO)(C(=O)C3(C)O)C)OC1=O
SMILES (Isomeric) CC1C2C(C3C4C(C(=O)CC56CC78C(CCC5C(C4(O2)O6)O)C(OC7CC(=O)O8)(C)CO)(C(=O)C3(C)O)C)OC1=O
InChI InChI=1S/C29H36O12/c1-11-18-19(37-22(11)34)17-20-25(3,23(35)26(17,4)36)14(31)8-27-9-28-13(6-5-12(27)21(33)29(20,40-18)41-27)24(2,10-30)38-15(28)7-16(32)39-28/h11-13,15,17-21,30,33,36H,5-10H2,1-4H3
InChI Key ZGUYNIIFXPYCNB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C29H36O12
Molecular Weight 576.60 g/mol
Exact Mass 576.22067658 g/mol
Topological Polar Surface Area (TPSA) 175.00 Ų
XlogP -1.20
Atomic LogP (AlogP) -0.43
H-Bond Acceptor 12
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 14,23-Dihydroxy-9-(hydroxymethyl)-9,18,23,25-tetramethyl-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacosane-5,19,24,26-tetrone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8387 83.87%
Caco-2 - 0.8193 81.93%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8032 80.32%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.8526 85.26%
OATP1B3 inhibitior + 0.9228 92.28%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6217 62.17%
BSEP inhibitior + 0.8405 84.05%
P-glycoprotein inhibitior + 0.6477 64.77%
P-glycoprotein substrate + 0.6268 62.68%
CYP3A4 substrate + 0.7017 70.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8744 87.44%
CYP3A4 inhibition - 0.8752 87.52%
CYP2C9 inhibition - 0.8943 89.43%
CYP2C19 inhibition - 0.9125 91.25%
CYP2D6 inhibition - 0.9712 97.12%
CYP1A2 inhibition - 0.8370 83.70%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.9783 97.83%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6127 61.27%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9139 91.39%
Skin irritation - 0.6322 63.22%
Skin corrosion - 0.9195 91.95%
Ames mutagenesis - 0.5670 56.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5558 55.58%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.5793 57.93%
skin sensitisation - 0.9397 93.97%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.7525 75.25%
Acute Oral Toxicity (c) III 0.4010 40.10%
Estrogen receptor binding + 0.7492 74.92%
Androgen receptor binding + 0.7444 74.44%
Thyroid receptor binding - 0.4939 49.39%
Glucocorticoid receptor binding + 0.6634 66.34%
Aromatase binding + 0.7412 74.12%
PPAR gamma + 0.6483 64.83%
Honey bee toxicity - 0.7257 72.57%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.8726 87.26%

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 96.38% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.75% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.21% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 94.89% 96.61%
CHEMBL1937 Q92769 Histone deacetylase 2 93.37% 94.75%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.34% 92.94%
CHEMBL299 P17252 Protein kinase C alpha 91.59% 98.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.76% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.27% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.73% 86.33%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 87.59% 95.83%
CHEMBL1902 P62942 FK506-binding protein 1A 86.44% 97.05%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.41% 100.00%
CHEMBL2581 P07339 Cathepsin D 86.28% 98.95%
CHEMBL325 Q13547 Histone deacetylase 1 85.25% 95.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.23% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.86% 89.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.54% 93.04%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.42% 93.00%

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.
Schisandra propinqua
Schisandra sphenanthera

Cross-Links

Top
PubChem 73070681
LOTUS LTS0013494
wikiData Q105375444