CID 163045487

Details

Top
Internal ID d0b408eb-7171-4cbe-84fd-00bc1a128442
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Dicarboxylic acids and derivatives
IUPAC Name
SMILES (Canonical) CC1CC(C2(C(C13CC(OC3O)C4=COC=C4)CCC(C25CO5)OC(=O)C)COC(=O)C)O
SMILES (Isomeric) CC1CC(C2(C(C13CC(OC3O)C4=COC=C4)CCC(C25CO5)OC(=O)C)COC(=O)C)O
InChI InChI=1S/C24H32O9/c1-13-8-19(27)23(11-30-14(2)25)18(4-5-20(32-15(3)26)24(23)12-31-24)22(13)9-17(33-21(22)28)16-6-7-29-10-16/h6-7,10,13,17-21,27-28H,4-5,8-9,11-12H2,1-3H3
InChI Key NZHRQVNIWJSSCR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C24H32O9
Molecular Weight 464.50 g/mol
Exact Mass 464.20463259 g/mol
Topological Polar Surface Area (TPSA) 128.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of CID 163045487

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9613 96.13%
Caco-2 - 0.7615 76.15%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8153 81.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7855 78.55%
OATP1B3 inhibitior + 0.8906 89.06%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8287 82.87%
BSEP inhibitior + 0.8431 84.31%
P-glycoprotein inhibitior - 0.5399 53.99%
P-glycoprotein substrate + 0.5440 54.40%
CYP3A4 substrate + 0.6682 66.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8395 83.95%
CYP3A4 inhibition + 0.6074 60.74%
CYP2C9 inhibition - 0.7210 72.10%
CYP2C19 inhibition - 0.7784 77.84%
CYP2D6 inhibition - 0.9512 95.12%
CYP1A2 inhibition - 0.8954 89.54%
CYP2C8 inhibition + 0.5963 59.63%
CYP inhibitory promiscuity - 0.8975 89.75%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4950 49.50%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.9389 93.89%
Skin irritation - 0.6905 69.05%
Skin corrosion - 0.9476 94.76%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6992 69.92%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5194 51.94%
skin sensitisation - 0.9281 92.81%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.4899 48.99%
Acute Oral Toxicity (c) I 0.5954 59.54%
Estrogen receptor binding + 0.9050 90.50%
Androgen receptor binding + 0.7011 70.11%
Thyroid receptor binding + 0.5840 58.40%
Glucocorticoid receptor binding + 0.8412 84.12%
Aromatase binding + 0.7005 70.05%
PPAR gamma + 0.6141 61.41%
Honey bee toxicity - 0.7979 79.79%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9867 98.67%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.77% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.64% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.57% 97.09%
CHEMBL2581 P07339 Cathepsin D 92.10% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.99% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.55% 96.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.67% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.41% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.28% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.31% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.26% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.12% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.03% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 81.77% 91.19%
CHEMBL5028 O14672 ADAM10 81.28% 97.50%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.28% 97.28%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.24% 85.14%

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.
Mutisia friesiana
Teucrium polium

Cross-Links

Top
PubChem 163045487
LOTUS LTS0244974
wikiData Q105137944