Xylaric acid A

Details

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Internal ID f50eca82-61a9-413f-9aab-b10202ce3014
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (4aS,5R,8S,8aR)-8-hydroxy-8-(hydroxymethyl)-5-propan-2-yl-2,4a,5,6,7,8a-hexahydrochromene-3-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H22O5/c1-8(2)10-3-4-14(18,7-15)12-11(10)5-9(6-19-12)13(16)17/h5,8,10-12,15,18H,3-4,6-7H2,1-2H3,(H,16,17)/t10-,11-,12-,14+/m1/s1
InChI Key PIOOXQKLTYQUAP-BYNQJWBRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22O5
Molecular Weight 270.32 g/mol
Exact Mass 270.14672380 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.80
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Xylaric acid A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8975 89.75%
Caco-2 - 0.5218 52.18%
Blood Brain Barrier - 0.5822 58.22%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8403 84.03%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9093 90.93%
OATP1B3 inhibitior + 0.8750 87.50%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7096 70.96%
BSEP inhibitior - 0.8504 85.04%
P-glycoprotein inhibitior - 0.9396 93.96%
P-glycoprotein substrate - 0.8437 84.37%
CYP3A4 substrate + 0.5362 53.62%
CYP2C9 substrate - 0.7936 79.36%
CYP2D6 substrate - 0.9051 90.51%
CYP3A4 inhibition - 0.9449 94.49%
CYP2C9 inhibition - 0.9008 90.08%
CYP2C19 inhibition - 0.8374 83.74%
CYP2D6 inhibition - 0.8911 89.11%
CYP1A2 inhibition - 0.8025 80.25%
CYP2C8 inhibition - 0.9273 92.73%
CYP inhibitory promiscuity - 0.9695 96.95%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6780 67.80%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.8436 84.36%
Skin irritation - 0.7205 72.05%
Skin corrosion - 0.9532 95.32%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8194 81.94%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.6343 63.43%
skin sensitisation - 0.8181 81.81%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7406 74.06%
Acute Oral Toxicity (c) III 0.6303 63.03%
Estrogen receptor binding + 0.6327 63.27%
Androgen receptor binding + 0.6012 60.12%
Thyroid receptor binding + 0.6568 65.68%
Glucocorticoid receptor binding + 0.6336 63.36%
Aromatase binding - 0.6382 63.82%
PPAR gamma - 0.5429 54.29%
Honey bee toxicity - 0.9393 93.93%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.8436 84.36%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.91% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.44% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.49% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.39% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.98% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 87.29% 95.93%
CHEMBL2581 P07339 Cathepsin D 86.12% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.09% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 82.15% 90.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.10% 93.00%

Plants that contains it

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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

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PubChem 139583529
LOTUS LTS0231986
wikiData Q75063588