Xylarioic acid B

Details

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Internal ID 4e03bc71-56bb-4fe9-8194-2c1a580dcbd2
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name 3,4,5-trihydroxy-2,4,6-trimethyloctanoic acid
SMILES (Canonical) CCC(C)C(C(C)(C(C(C)C(=O)O)O)O)O
SMILES (Isomeric) CCC(C)C(C(C)(C(C(C)C(=O)O)O)O)O
InChI InChI=1S/C11H22O5/c1-5-6(2)8(12)11(4,16)9(13)7(3)10(14)15/h6-9,12-13,16H,5H2,1-4H3,(H,14,15)
InChI Key GQRHWZJLXPDUAP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H22O5
Molecular Weight 234.29 g/mol
Exact Mass 234.14672380 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.23
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Xylarioic acid B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6963 69.63%
Caco-2 - 0.7891 78.91%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6329 63.29%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.8361 83.61%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9577 95.77%
P-glycoprotein inhibitior - 0.9362 93.62%
P-glycoprotein substrate - 0.9160 91.60%
CYP3A4 substrate - 0.6700 67.00%
CYP2C9 substrate - 0.5759 57.59%
CYP2D6 substrate - 0.8745 87.45%
CYP3A4 inhibition - 0.8099 80.99%
CYP2C9 inhibition - 0.7695 76.95%
CYP2C19 inhibition - 0.8766 87.66%
CYP2D6 inhibition - 0.9194 91.94%
CYP1A2 inhibition - 0.8474 84.74%
CYP2C8 inhibition - 0.9544 95.44%
CYP inhibitory promiscuity - 0.9079 90.79%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7523 75.23%
Carcinogenicity (trinary) Non-required 0.6394 63.94%
Eye corrosion - 0.9270 92.70%
Eye irritation - 0.9518 95.18%
Skin irritation - 0.6667 66.67%
Skin corrosion - 0.8996 89.96%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7880 78.80%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation - 0.7177 71.77%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6171 61.71%
Acute Oral Toxicity (c) III 0.8312 83.12%
Estrogen receptor binding - 0.4887 48.87%
Androgen receptor binding - 0.6610 66.10%
Thyroid receptor binding - 0.5709 57.09%
Glucocorticoid receptor binding - 0.6304 63.04%
Aromatase binding - 0.6921 69.21%
PPAR gamma - 0.6600 66.00%
Honey bee toxicity - 0.9687 96.87%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity + 0.7232 72.32%

Targets

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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
CHEMBL2581 P07339 Cathepsin D 96.15% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.55% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.40% 97.25%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 91.13% 100.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.31% 97.29%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 86.53% 98.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.46% 93.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.28% 96.47%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.06% 85.14%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 46832764
LOTUS LTS0162989
wikiData Q104167394