Aphidicolin-17-acetate

Details

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Internal ID 0d0715d6-dd55-478e-bbd9-7babcd256f45
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Aphidicolane and stemodane diterpenoids
IUPAC Name [(1S,2S,5R,6R,7R,10S,12R,13S)-5,13-dihydroxy-6-(hydroxymethyl)-2,6-dimethyl-13-tetracyclo[10.3.1.01,10.02,7]hexadecanyl]methyl acetate
SMILES (Canonical) CC(=O)OCC1(CCC23CC1CC2CCC4C3(CCC(C4(C)CO)O)C)O
SMILES (Isomeric) CC(=O)OC[C@@]1(CC[C@]23C[C@H]1C[C@@H]2CC[C@@H]4[C@@]3(CC[C@H]([C@@]4(C)CO)O)C)O
InChI InChI=1S/C22H36O5/c1-14(24)27-13-22(26)9-8-21-11-16(22)10-15(21)4-5-17-19(2,12-23)18(25)6-7-20(17,21)3/h15-18,23,25-26H,4-13H2,1-3H3/t15-,16+,17-,18+,19-,20-,21-,22+/m0/s1
InChI Key GAPINCSXTLCIPV-YZWRWILZSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C22H36O5
Molecular Weight 380.50 g/mol
Exact Mass 380.25627424 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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Aphidicolin-17-acetate
51103-57-2
8,11a-Methano-11aH-cyclohepta(a)naphthalene-4,9-dimethanol, tetradecahydro-3,9-dihydroxy-4,11b-dimethyl-, alpha9-acetate, (3alpha,4alpha,4aalpha,6abeta,8beta,9beta,11abeta,11bbeta)-

2D Structure

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2D Structure of Aphidicolin-17-acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9211 92.11%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6776 67.76%
OATP2B1 inhibitior - 0.8641 86.41%
OATP1B1 inhibitior + 0.8954 89.54%
OATP1B3 inhibitior + 0.9093 90.93%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7090 70.90%
P-glycoprotein inhibitior - 0.8211 82.11%
P-glycoprotein substrate - 0.5476 54.76%
CYP3A4 substrate + 0.7101 71.01%
CYP2C9 substrate - 0.8163 81.63%
CYP2D6 substrate - 0.8503 85.03%
CYP3A4 inhibition - 0.9045 90.45%
CYP2C9 inhibition - 0.7639 76.39%
CYP2C19 inhibition - 0.7208 72.08%
CYP2D6 inhibition - 0.9649 96.49%
CYP1A2 inhibition - 0.8548 85.48%
CYP2C8 inhibition - 0.5770 57.70%
CYP inhibitory promiscuity - 0.9485 94.85%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7241 72.41%
Eye corrosion - 0.9936 99.36%
Eye irritation - 0.9303 93.03%
Skin irritation - 0.5809 58.09%
Skin corrosion - 0.9624 96.24%
Ames mutagenesis - 0.7154 71.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5748 57.48%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.7830 78.30%
skin sensitisation - 0.9367 93.67%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.4643 46.43%
Acute Oral Toxicity (c) III 0.5176 51.76%
Estrogen receptor binding + 0.9074 90.74%
Androgen receptor binding + 0.5913 59.13%
Thyroid receptor binding + 0.6046 60.46%
Glucocorticoid receptor binding + 0.8336 83.36%
Aromatase binding + 0.7892 78.92%
PPAR gamma - 0.6228 62.28%
Honey bee toxicity - 0.7482 74.82%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5107 51.07%
Fish aquatic toxicity + 0.9359 93.59%

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 97.36% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 96.75% 96.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.44% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.37% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.85% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.84% 82.69%
CHEMBL299 P17252 Protein kinase C alpha 90.83% 98.03%
CHEMBL340 P08684 Cytochrome P450 3A4 89.47% 91.19%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.53% 94.62%
CHEMBL3437 Q16853 Amine oxidase, copper containing 88.41% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.42% 94.45%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 87.29% 95.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.83% 100.00%
CHEMBL4040 P28482 MAP kinase ERK2 85.15% 83.82%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.10% 92.86%
CHEMBL233 P35372 Mu opioid receptor 84.32% 97.93%
CHEMBL2996 Q05655 Protein kinase C delta 83.83% 97.79%
CHEMBL1937 Q92769 Histone deacetylase 2 83.54% 94.75%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.15% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.85% 92.62%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 81.28% 89.05%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.60% 97.21%
CHEMBL1914 P06276 Butyrylcholinesterase 80.35% 95.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.30% 97.29%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.17% 95.89%

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 118987258
LOTUS LTS0111830
wikiData Q104403159