Xylaranic acid

Details

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Internal ID 9f09551f-a8a5-47ac-9a5a-88f0fe8dc7aa
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name 2-[(2R,3S,6S,8S,8aR)-3,6-dihydroxy-8,8a-dimethyl-2,3,5,6,7,8-hexahydro-1H-naphthalen-2-yl]-3-hydroxypropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O5/c1-8-3-10(17)4-9-5-13(18)11(6-15(8,9)2)12(7-16)14(19)20/h5,8,10-13,16-18H,3-4,6-7H2,1-2H3,(H,19,20)/t8-,10-,11+,12?,13+,15+/m0/s1
InChI Key DPKPTGARWFZSLN-NYBSVRFASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O5
Molecular Weight 284.35 g/mol
Exact Mass 284.16237386 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.78
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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RefChem:195414
CHEBI:218850
2-[(2R,3S,6S,8S,8aR)-3,6-dihydroxy-8,8a-dimethyl-2,3,5,6,7,8-hexahydro-1H-naphthalen-2-yl]-3-hydroxypropanoic acid

2D Structure

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2D Structure of Xylaranic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9859 98.59%
Caco-2 + 0.5997 59.97%
Blood Brain Barrier + 0.5550 55.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7909 79.09%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.8434 84.34%
OATP1B3 inhibitior + 0.8160 81.60%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8747 87.47%
BSEP inhibitior - 0.9385 93.85%
P-glycoprotein inhibitior - 0.9590 95.90%
P-glycoprotein substrate - 0.7175 71.75%
CYP3A4 substrate + 0.5393 53.93%
CYP2C9 substrate - 0.6653 66.53%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition - 0.8581 85.81%
CYP2C9 inhibition - 0.9163 91.63%
CYP2C19 inhibition - 0.9101 91.01%
CYP2D6 inhibition - 0.9300 93.00%
CYP1A2 inhibition - 0.8890 88.90%
CYP2C8 inhibition - 0.8616 86.16%
CYP inhibitory promiscuity - 0.8883 88.83%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6821 68.21%
Eye corrosion - 0.9930 99.30%
Eye irritation - 0.9506 95.06%
Skin irritation - 0.5907 59.07%
Skin corrosion - 0.9608 96.08%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5829 58.29%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6692 66.92%
skin sensitisation - 0.8499 84.99%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.7579 75.79%
Acute Oral Toxicity (c) III 0.7001 70.01%
Estrogen receptor binding - 0.5566 55.66%
Androgen receptor binding + 0.5545 55.45%
Thyroid receptor binding - 0.5195 51.95%
Glucocorticoid receptor binding - 0.4919 49.19%
Aromatase binding - 0.5430 54.30%
PPAR gamma - 0.8199 81.99%
Honey bee toxicity - 0.8670 86.70%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9902 99.02%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.86% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.21% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.15% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.26% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.64% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.81% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.19% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.05% 95.56%
CHEMBL220 P22303 Acetylcholinesterase 81.07% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.86% 100.00%

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 46217967
LOTUS LTS0045588
wikiData Q77567092