Annosquamosin E

Details

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Internal ID 7b9bfeca-8e85-4cae-a0f7-dabc209db8d2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name [(1S,4S,5R,9S,10R,13R,14S)-5-formyloxy-14-hydroxy-5,9-dimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate
SMILES (Canonical) CC(=O)OCC1(CC23CCC4C(C2CCC1C3)(CCCC4(C)OC=O)C)O
SMILES (Isomeric) CC(=O)OC[C@@]1(C[C@@]23CC[C@H]4[C@]([C@@H]2CC[C@@H]1C3)(CCC[C@@]4(C)OC=O)C)O
InChI InChI=1S/C22H34O5/c1-15(24)26-13-22(25)12-21-10-7-17-19(2,18(21)6-5-16(22)11-21)8-4-9-20(17,3)27-14-23/h14,16-18,25H,4-13H2,1-3H3/t16-,17+,18+,19-,20-,21+,22-/m1/s1
InChI Key CGCFVZINVXIAQC-FSCQIMEVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H34O5
Molecular Weight 378.50 g/mol
Exact Mass 378.24062418 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.62
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Annosquamosin E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 + 0.5732 57.32%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8279 82.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8961 89.61%
OATP1B3 inhibitior + 0.9473 94.73%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7114 71.14%
BSEP inhibitior + 0.7555 75.55%
P-glycoprotein inhibitior - 0.6456 64.56%
P-glycoprotein substrate - 0.6994 69.94%
CYP3A4 substrate + 0.6593 65.93%
CYP2C9 substrate + 0.5528 55.28%
CYP2D6 substrate - 0.8538 85.38%
CYP3A4 inhibition - 0.8630 86.30%
CYP2C9 inhibition - 0.8079 80.79%
CYP2C19 inhibition - 0.8202 82.02%
CYP2D6 inhibition - 0.9656 96.56%
CYP1A2 inhibition - 0.8705 87.05%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.9574 95.74%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7288 72.88%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.9545 95.45%
Skin irritation - 0.5762 57.62%
Skin corrosion - 0.9625 96.25%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5813 58.13%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.7301 73.01%
skin sensitisation - 0.9107 91.07%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7202 72.02%
Acute Oral Toxicity (c) III 0.5860 58.60%
Estrogen receptor binding + 0.9063 90.63%
Androgen receptor binding + 0.5491 54.91%
Thyroid receptor binding + 0.5544 55.44%
Glucocorticoid receptor binding + 0.8171 81.71%
Aromatase binding + 0.7351 73.51%
PPAR gamma - 0.5508 55.08%
Honey bee toxicity - 0.7990 79.90%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6355 63.55%
Fish aquatic toxicity + 0.9760 97.60%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.53% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.79% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.16% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.31% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.76% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.84% 82.69%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 87.68% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.59% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.42% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 84.49% 91.19%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.85% 94.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.42% 96.77%
CHEMBL5028 O14672 ADAM10 83.14% 97.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.62% 92.62%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.11% 93.00%
CHEMBL1937 Q92769 Histone deacetylase 2 81.97% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.87% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.71% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 80.26% 90.17%

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.
Annona squamosa

Cross-Links

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PubChem 10981748
NPASS NPC230170
LOTUS LTS0187281
wikiData Q104957473