Euscaphic acid A, (rel)-

Details

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Internal ID 2aa32d7c-061e-4e64-8060-af9e0b45d67e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1R,2R,5R,7S,10S,11R,14S,15S,16R,17R,20S)-7,16-dihydroxy-2,6,6,10,16,17-hexamethylhexacyclo[12.8.1.01,14.02,11.05,10.015,20]tricos-12-ene-20-carboxylic acid
SMILES (Canonical) CC1CCC2(CCC34CC3(C2C1(C)O)C=CC5C4(CCC6C5(CCC(C6(C)C)O)C)C)C(=O)O
SMILES (Isomeric) C[C@@H]1CC[C@@]2(CC[C@]34C[C@@]3([C@@H]2[C@]1(C)O)C=C[C@H]5[C@]4(CC[C@@H]6[C@@]5(CC[C@@H](C6(C)C)O)C)C)C(=O)O
InChI InChI=1S/C30H46O4/c1-18-7-13-28(23(32)33)15-16-30-17-29(30,22(28)27(18,6)34)14-9-20-25(4)11-10-21(31)24(2,3)19(25)8-12-26(20,30)5/h9,14,18-22,31,34H,7-8,10-13,15-17H2,1-6H3,(H,32,33)/t18-,19+,20-,21+,22-,25+,26-,27-,28+,29-,30-/m1/s1
InChI Key BDOLMVCDVYAFEX-WUHNTGCUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H46O4
Molecular Weight 470.70 g/mol
Exact Mass 470.33960994 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.81
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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CHEBI:70675
EUSCAPHIC ACID A
CHEMBL1270152
Q27139007

2D Structure

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2D Structure of Euscaphic acid A, (rel)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 - 0.5677 56.77%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8030 80.30%
OATP2B1 inhibitior - 0.7181 71.81%
OATP1B1 inhibitior + 0.8637 86.37%
OATP1B3 inhibitior + 0.9106 91.06%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7321 73.21%
BSEP inhibitior + 0.8622 86.22%
P-glycoprotein inhibitior - 0.7696 76.96%
P-glycoprotein substrate - 0.7559 75.59%
CYP3A4 substrate + 0.6828 68.28%
CYP2C9 substrate - 0.8080 80.80%
CYP2D6 substrate - 0.8562 85.62%
CYP3A4 inhibition - 0.7415 74.15%
CYP2C9 inhibition - 0.8493 84.93%
CYP2C19 inhibition - 0.8799 87.99%
CYP2D6 inhibition - 0.9607 96.07%
CYP1A2 inhibition - 0.7582 75.82%
CYP2C8 inhibition - 0.6053 60.53%
CYP inhibitory promiscuity - 0.9590 95.90%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7087 70.87%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9429 94.29%
Skin irritation + 0.5834 58.34%
Skin corrosion - 0.9498 94.98%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5439 54.39%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5528 55.28%
skin sensitisation - 0.5935 59.35%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7302 73.02%
Acute Oral Toxicity (c) III 0.7326 73.26%
Estrogen receptor binding + 0.8213 82.13%
Androgen receptor binding + 0.7210 72.10%
Thyroid receptor binding + 0.6212 62.12%
Glucocorticoid receptor binding + 0.7903 79.03%
Aromatase binding + 0.7129 71.29%
PPAR gamma + 0.6768 67.68%
Honey bee toxicity - 0.8523 85.23%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9950 99.50%

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 93.74% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.29% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.98% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.90% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.69% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.04% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.22% 86.33%
CHEMBL5028 O14672 ADAM10 81.01% 97.50%

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.
Staphylea japonica

Cross-Links

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PubChem 49831540
LOTUS LTS0119597
wikiData Q27139007