(20R,22R)-16beta-Acetoxy-3beta,4beta;5beta,6beta-diepoxy-12beta,20-dihydroxy-1-oxowith-24-enolide

Details

Top
Internal ID aadeff53-654e-4336-a520-c9a5f38ac038
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones
IUPAC Name [(1S,2R,5S,7S,8S,10R,12R,13S,15S,16R,17S,18R)-16-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-18-hydroxy-17-methyl-3-oxo-6,9-dioxahexacyclo[10.7.0.02,8.05,7.08,10.013,17]nonadecan-15-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H38O9/c1-11-6-21(37-26(33)12(11)2)28(5,34)24-18(35-13(3)30)9-16-14-8-22-29(38-22)23(17(31)10-19-25(29)36-19)15(14)7-20(32)27(16,24)4/h14-16,18-25,32,34H,6-10H2,1-5H3/t14-,15+,16+,18+,19+,20-,21-,22-,23+,24+,25+,27-,28+,29-/m1/s1
InChI Key FIMAYHJYWNSMFM-NNLREDAASA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C29H38O9
Molecular Weight 530.60 g/mol
Exact Mass 530.25158279 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.86
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
RefChem:905774
(20R,22R)-16beta-Acetoxy-3beta,4beta;5beta,6beta-diepoxy-12beta,20-dihydroxy-1-oxowith-24-enolide
CHEMBL1172383

2D Structure

Top
2D Structure of (20R,22R)-16beta-Acetoxy-3beta,4beta;5beta,6beta-diepoxy-12beta,20-dihydroxy-1-oxowith-24-enolide

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9678 96.78%
Caco-2 - 0.7613 76.13%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6392 63.92%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.8833 88.33%
OATP1B3 inhibitior + 0.8828 88.28%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8344 83.44%
P-glycoprotein inhibitior + 0.6469 64.69%
P-glycoprotein substrate + 0.6135 61.35%
CYP3A4 substrate + 0.7480 74.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8986 89.86%
CYP3A4 inhibition - 0.6014 60.14%
CYP2C9 inhibition - 0.8555 85.55%
CYP2C19 inhibition - 0.8719 87.19%
CYP2D6 inhibition - 0.9511 95.11%
CYP1A2 inhibition - 0.8285 82.85%
CYP2C8 inhibition + 0.6168 61.68%
CYP inhibitory promiscuity - 0.9517 95.17%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5749 57.49%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9372 93.72%
Skin irritation - 0.5294 52.94%
Skin corrosion - 0.9244 92.44%
Ames mutagenesis - 0.5944 59.44%
Human Ether-a-go-go-Related Gene inhibition - 0.4144 41.44%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8177 81.77%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.9421 94.21%
Acute Oral Toxicity (c) I 0.5723 57.23%
Estrogen receptor binding + 0.7743 77.43%
Androgen receptor binding + 0.7095 70.95%
Thyroid receptor binding - 0.5609 56.09%
Glucocorticoid receptor binding + 0.6949 69.49%
Aromatase binding + 0.7035 70.35%
PPAR gamma + 0.7111 71.11%
Honey bee toxicity - 0.5922 59.22%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9866 98.66%

Targets

Top

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.71% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.03% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 91.79% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 91.66% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.92% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.26% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.62% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.66% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.14% 99.23%
CHEMBL5028 O14672 ADAM10 84.83% 97.50%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.23% 91.07%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.60% 97.14%
CHEMBL2996 Q05655 Protein kinase C delta 83.03% 97.79%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.02% 93.04%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.96% 94.08%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.35% 94.00%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.87% 90.93%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.58% 100.00%

Plants that contains it

Top
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.
Iochroma arborescens

Cross-Links

Top
PubChem 49799449
NPASS NPC469790
ChEMBL CHEMBL1172383
LOTUS LTS0101979
wikiData Q104995775