Adenolin D

Details

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Internal ID 3f49bbce-046f-4099-8428-3f5e620c316c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name [(1S,2S,3R,5R,6S,8S,9S,10S,11R)-9,10-dihydroxy-6-(methoxymethyl)-12,12-dimethyl-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-3-yl] acetate
SMILES (Canonical) CC(=O)OC1CC2CC3(C1C45CCCC(C4C(C3(OC5)O)O)(C)C)C(=O)C2COC
SMILES (Isomeric) CC(=O)O[C@@H]1C[C@H]2C[C@]3([C@@H]1[C@]45CCCC([C@H]4[C@@H]([C@]3(OC5)O)O)(C)C)C(=O)[C@@H]2COC
InChI InChI=1S/C23H34O7/c1-12(24)30-15-8-13-9-22(18(25)14(13)10-28-4)16(15)21-7-5-6-20(2,3)17(21)19(26)23(22,27)29-11-21/h13-17,19,26-27H,5-11H2,1-4H3/t13-,14+,15+,16-,17+,19-,21+,22-,23+/m0/s1
InChI Key VVSBOWDVUWUVCK-ZTDGPNIRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H34O7
Molecular Weight 422.50 g/mol
Exact Mass 422.23045342 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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CHEBI:67674
Q27136146

2D Structure

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2D Structure of Adenolin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7596 75.96%
Caco-2 - 0.5509 55.09%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8066 80.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8583 85.83%
OATP1B3 inhibitior + 0.8990 89.90%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6285 62.85%
P-glycoprotein inhibitior - 0.6933 69.33%
P-glycoprotein substrate - 0.5554 55.54%
CYP3A4 substrate + 0.7062 70.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition - 0.8984 89.84%
CYP2C9 inhibition - 0.7951 79.51%
CYP2C19 inhibition - 0.8010 80.10%
CYP2D6 inhibition - 0.9633 96.33%
CYP1A2 inhibition - 0.8367 83.67%
CYP2C8 inhibition - 0.5745 57.45%
CYP inhibitory promiscuity - 0.9840 98.40%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6864 68.64%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9509 95.09%
Skin irritation - 0.7579 75.79%
Skin corrosion - 0.9478 94.78%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4781 47.81%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5566 55.66%
skin sensitisation - 0.9100 91.00%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.4885 48.85%
Acute Oral Toxicity (c) III 0.3586 35.86%
Estrogen receptor binding + 0.7981 79.81%
Androgen receptor binding + 0.7358 73.58%
Thyroid receptor binding + 0.5420 54.20%
Glucocorticoid receptor binding + 0.7385 73.85%
Aromatase binding + 0.6549 65.49%
PPAR gamma + 0.6477 64.77%
Honey bee toxicity - 0.7610 76.10%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9235 92.35%

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 97.60% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.32% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.96% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.82% 97.25%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.32% 91.07%
CHEMBL3922 P50579 Methionine aminopeptidase 2 90.47% 97.28%
CHEMBL340 P08684 Cytochrome P450 3A4 90.03% 91.19%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.53% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.48% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.24% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.76% 96.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.59% 99.23%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.46% 91.24%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 85.76% 95.71%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.20% 94.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.86% 94.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 84.42% 96.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.00% 82.69%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.29% 94.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.03% 100.00%
CHEMBL1871 P10275 Androgen Receptor 82.66% 96.43%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.72% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.47% 85.14%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.31% 94.08%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.15% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.01% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.38% 92.62%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.30% 93.04%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.18% 97.14%

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.
Isodon adenolomus
Isodon lihsienensis

Cross-Links

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PubChem 70698028
LOTUS LTS0161855
wikiData Q27136146