Capillolide

Details

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Internal ID 7634a48a-fa7c-4b92-b624-ccf4c557ff22
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (1R,3R,4S,7E,11S,12R)-3,4,11-trihydroxy-4,8,12-trimethyl-15-methylidene-13-oxabicyclo[10.3.2]heptadec-7-en-14-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O5/c1-13-6-5-10-19(3,24)17(22)12-15-9-11-20(4,16(21)8-7-13)25-18(23)14(15)2/h6,15-17,21-22,24H,2,5,7-12H2,1,3-4H3/b13-6+/t15-,16+,17-,19+,20-/m1/s1
InChI Key JLCJNFREUBTKDT-WRHAGOLESA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O5
Molecular Weight 352.50 g/mol
Exact Mass 352.22497412 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.64
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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CHEBI:65575
CHEMBL519044
Q27134031
(1R,3R,4S,7E,11S,12R)-3,4,11-trihydroxy-4,8,12-trimethyl-15-methylidene-13-oxabicyclo[10.3.2]heptadec-7-en-14-one

2D Structure

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2D Structure of Capillolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9470 94.70%
Caco-2 + 0.6378 63.78%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6121 61.21%
OATP2B1 inhibitior - 0.8681 86.81%
OATP1B1 inhibitior + 0.9405 94.05%
OATP1B3 inhibitior + 0.9185 91.85%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6571 65.71%
BSEP inhibitior - 0.4814 48.14%
P-glycoprotein inhibitior - 0.8078 80.78%
P-glycoprotein substrate - 0.8076 80.76%
CYP3A4 substrate + 0.6476 64.76%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.8587 85.87%
CYP3A4 inhibition - 0.6286 62.86%
CYP2C9 inhibition - 0.7676 76.76%
CYP2C19 inhibition - 0.6194 61.94%
CYP2D6 inhibition - 0.9411 94.11%
CYP1A2 inhibition + 0.5200 52.00%
CYP2C8 inhibition - 0.6032 60.32%
CYP inhibitory promiscuity - 0.9833 98.33%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6603 66.03%
Eye corrosion - 0.9864 98.64%
Eye irritation - 0.9087 90.87%
Skin irritation + 0.5508 55.08%
Skin corrosion - 0.9285 92.85%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4352 43.52%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5047 50.47%
skin sensitisation - 0.7118 71.18%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.5887 58.87%
Acute Oral Toxicity (c) III 0.5187 51.87%
Estrogen receptor binding + 0.7864 78.64%
Androgen receptor binding + 0.5369 53.69%
Thyroid receptor binding + 0.6610 66.10%
Glucocorticoid receptor binding + 0.9075 90.75%
Aromatase binding + 0.7125 71.25%
PPAR gamma + 0.5352 53.52%
Honey bee toxicity - 0.9112 91.12%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9809 98.09%

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 96.40% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.66% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.62% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.83% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.66% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.99% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.78% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.14% 99.23%
CHEMBL1871 P10275 Androgen Receptor 85.61% 96.43%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.80% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.36% 92.94%
CHEMBL5028 O14672 ADAM10 80.34% 97.50%

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 11792322
LOTUS LTS0206059
wikiData Q27134031