Curvulide B2

Details

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Internal ID 5cb79264-9040-4f51-8702-5e99377e0d0f
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Alpha,beta-unsaturated carboxylic esters > Enoate esters
IUPAC Name (1R,2R,5Z,7R,10R)-7-hydroxy-2-methyl-3-oxabicyclo[8.1.0]undeca-5,8-dien-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H14O3/c1-7-10-6-8(10)2-3-9(12)4-5-11(13)14-7/h2-5,7-10,12H,6H2,1H3/b3-2?,5-4-/t7-,8+,9-,10+/m1/s1
InChI Key MDQSATBZDUKXGN-XQRARYDUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O3
Molecular Weight 194.23 g/mol
Exact Mass 194.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.04
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Curvulide B2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.7189 71.89%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.4287 42.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8979 89.79%
OATP1B3 inhibitior + 0.9760 97.60%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9677 96.77%
P-glycoprotein inhibitior - 0.9763 97.63%
P-glycoprotein substrate - 0.9151 91.51%
CYP3A4 substrate - 0.5517 55.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8916 89.16%
CYP3A4 inhibition - 0.9553 95.53%
CYP2C9 inhibition - 0.9484 94.84%
CYP2C19 inhibition - 0.9160 91.60%
CYP2D6 inhibition - 0.9651 96.51%
CYP1A2 inhibition - 0.6784 67.84%
CYP2C8 inhibition - 0.9757 97.57%
CYP inhibitory promiscuity - 0.9777 97.77%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8317 83.17%
Carcinogenicity (trinary) Non-required 0.5437 54.37%
Eye corrosion + 0.6737 67.37%
Eye irritation - 0.8156 81.56%
Skin irritation + 0.7678 76.78%
Skin corrosion - 0.5808 58.08%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6867 68.67%
Micronuclear + 0.5100 51.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.5775 57.75%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6058 60.58%
Acute Oral Toxicity (c) II 0.4352 43.52%
Estrogen receptor binding - 0.7789 77.89%
Androgen receptor binding - 0.8107 81.07%
Thyroid receptor binding - 0.8276 82.76%
Glucocorticoid receptor binding - 0.6121 61.21%
Aromatase binding - 0.8891 88.91%
PPAR gamma - 0.8121 81.21%
Honey bee toxicity - 0.9052 90.52%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.6482 64.82%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.59% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.44% 95.56%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 85.49% 87.67%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.43% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.26% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.50% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.19% 86.33%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.19% 81.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.03% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.23% 89.00%

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 139586492
LOTUS LTS0139253
wikiData Q105161914