Viscosalactone B

Details

Top
Internal ID f9b9d473-c6f2-49a2-bd89-9f07a996036a
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name (1S,2R,5S,6S,7R,9R,11S,12S,15R,16S)-5,6-dihydroxy-15-[(1S)-1-[(2R)-5-(hydroxymethyl)-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one
SMILES (Canonical) CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)O)C)O5)C)CO
SMILES (Isomeric) CC1=C(C(=O)O[C@H](C1)[C@@H](C)[C@H]2CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3C[C@@H]5[C@]6([C@@]4(C(=O)C[C@@H]([C@@H]6O)O)C)O5)C)CO
InChI InChI=1S/C28H40O7/c1-13-9-21(34-25(33)16(13)12-29)14(2)17-5-6-18-15-10-23-28(35-23)24(32)20(30)11-22(31)27(28,4)19(15)7-8-26(17,18)3/h14-15,17-21,23-24,29-30,32H,5-12H2,1-4H3/t14-,15-,17+,18-,19-,20-,21+,23+,24-,26+,27-,28-/m0/s1
InChI Key WVMINIQLCDVTLH-IVFYTCICSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C28H40O7
Molecular Weight 488.60 g/mol
Exact Mass 488.27740361 g/mol
Topological Polar Surface Area (TPSA) 117.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.55
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
CHEBI:69122
CHEMBL1934584
WVMINIQLCDVTLH-IVFYTCICSA-N
76938-46-0
Q27137462
(3beta,4beta,5beta,6beta,22R)-3,4,27-trihydroxy-5,6:22,26-diepoxyergost-24-ene-1,26-dione

2D Structure

Top
2D Structure of Viscosalactone B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8868 88.68%
Caco-2 - 0.7386 73.86%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7598 75.98%
OATP2B1 inhibitior - 0.5635 56.35%
OATP1B1 inhibitior + 0.8423 84.23%
OATP1B3 inhibitior + 0.9331 93.31%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6079 60.79%
BSEP inhibitior + 0.7765 77.65%
P-glycoprotein inhibitior - 0.4906 49.06%
P-glycoprotein substrate + 0.5736 57.36%
CYP3A4 substrate + 0.7274 72.74%
CYP2C9 substrate - 0.8259 82.59%
CYP2D6 substrate - 0.8882 88.82%
CYP3A4 inhibition - 0.6932 69.32%
CYP2C9 inhibition - 0.8180 81.80%
CYP2C19 inhibition - 0.9048 90.48%
CYP2D6 inhibition - 0.9511 95.11%
CYP1A2 inhibition - 0.8499 84.99%
CYP2C8 inhibition - 0.5697 56.97%
CYP inhibitory promiscuity - 0.9760 97.60%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5877 58.77%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9483 94.83%
Skin irritation + 0.5549 55.49%
Skin corrosion - 0.9342 93.42%
Ames mutagenesis - 0.5402 54.02%
Human Ether-a-go-go-Related Gene inhibition + 0.6463 64.63%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.6405 64.05%
skin sensitisation - 0.8926 89.26%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) I 0.5720 57.20%
Estrogen receptor binding + 0.6578 65.78%
Androgen receptor binding + 0.7692 76.92%
Thyroid receptor binding - 0.5099 50.99%
Glucocorticoid receptor binding + 0.7030 70.30%
Aromatase binding + 0.7105 71.05%
PPAR gamma + 0.6049 60.49%
Honey bee toxicity - 0.7747 77.47%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9630 96.30%

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
CHEMBL204 P00734 Thrombin 96.50% 96.01%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.34% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 91.63% 94.75%
CHEMBL5103 Q969S8 Histone deacetylase 10 91.38% 90.08%
CHEMBL2581 P07339 Cathepsin D 91.25% 98.95%
CHEMBL3837 P07711 Cathepsin L 91.20% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.05% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.01% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 90.50% 97.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.24% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.15% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.00% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.24% 93.04%
CHEMBL325 Q13547 Histone deacetylase 1 86.03% 95.92%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.59% 100.00%
CHEMBL299 P17252 Protein kinase C alpha 84.46% 98.03%
CHEMBL3310 Q96DB2 Histone deacetylase 11 84.43% 88.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.42% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.38% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.33% 97.25%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.20% 93.03%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.10% 93.56%
CHEMBL221 P23219 Cyclooxygenase-1 81.81% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.13% 86.33%

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.
Physalis longifolia
Physalis peruviana
Withania somnifera

Cross-Links

Top
PubChem 57403080
LOTUS LTS0051965
wikiData Q27137462