1,3,14-Trihydroxycard-20(22)-enolide

Details

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Internal ID c5b969df-1691-46c6-8756-3fec80843f57
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Cardenolides and derivatives
IUPAC Name 3-[(1R,3R,5R,10S,13R,14S,17R)-1,3,14-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H34O5/c1-21-7-5-17-18(4-3-14-10-15(24)11-19(25)22(14,17)2)23(21,27)8-6-16(21)13-9-20(26)28-12-13/h9,14-19,24-25,27H,3-8,10-12H2,1-2H3/t14-,15-,16-,17?,18?,19-,21-,22+,23+/m1/s1
InChI Key CSKIDXJFNAYMTR-YTAKEYINSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H34O5
Molecular Weight 390.50 g/mol
Exact Mass 390.24062418 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.58
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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1,3,14-Trihydroxycard-20(22)-enolide
RefChem:1052465
DTXCID501408088
1-beta-Hydroxydigitoxigenin
5-beta-CARD-20(22)-ENOLIDE, 1-beta,3-beta,14-TRIHYDROXY-
(8xi,9xi)-1beta,3beta,14-Trihydroxy-5beta-card-20(22)-enolide

2D Structure

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2D Structure of 1,3,14-Trihydroxycard-20(22)-enolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 - 0.5255 52.55%
Blood Brain Barrier - 0.6189 61.89%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8004 80.04%
OATP2B1 inhibitior - 0.7232 72.32%
OATP1B1 inhibitior + 0.9348 93.48%
OATP1B3 inhibitior + 0.9615 96.15%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7493 74.93%
BSEP inhibitior + 0.8106 81.06%
P-glycoprotein inhibitior - 0.9074 90.74%
P-glycoprotein substrate + 0.6555 65.55%
CYP3A4 substrate + 0.6748 67.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9060 90.60%
CYP3A4 inhibition - 0.8310 83.10%
CYP2C9 inhibition - 0.9099 90.99%
CYP2C19 inhibition - 0.9256 92.56%
CYP2D6 inhibition - 0.9362 93.62%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.7813 78.13%
CYP inhibitory promiscuity - 0.8702 87.02%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5443 54.43%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.9637 96.37%
Skin irritation - 0.5181 51.81%
Skin corrosion - 0.9360 93.60%
Ames mutagenesis - 0.7134 71.34%
Human Ether-a-go-go-Related Gene inhibition - 0.4887 48.87%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5036 50.36%
skin sensitisation - 0.8828 88.28%
Respiratory toxicity + 0.9333 93.33%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.7459 74.59%
Acute Oral Toxicity (c) I 0.5853 58.53%
Estrogen receptor binding + 0.8867 88.67%
Androgen receptor binding + 0.8389 83.89%
Thyroid receptor binding + 0.6181 61.81%
Glucocorticoid receptor binding + 0.8379 83.79%
Aromatase binding + 0.7124 71.24%
PPAR gamma + 0.5407 54.07%
Honey bee toxicity - 0.7657 76.57%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9889 98.89%

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
CHEMBL1994 P08235 Mineralocorticoid receptor 96.15% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 95.45% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.15% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.78% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.48% 96.09%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 90.73% 81.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.40% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.37% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.36% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.53% 86.33%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.89% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.38% 95.89%
CHEMBL1871 P10275 Androgen Receptor 84.67% 96.43%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.24% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.51% 99.23%
CHEMBL2581 P07339 Cathepsin D 81.43% 98.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.30% 90.71%

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.
Streptocaulon juventas

Cross-Links

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PubChem 12539
LOTUS LTS0275814
wikiData Q82966852