CID 163105058

Details

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Internal ID bcf661e9-79b8-4712-9186-38ff25b24560
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name
SMILES (Canonical) CC(=O)OC1(C(=O)C(=C)C2C(CCCC2(C13CCC4(O3)CC(OC4)OC)C)(C)C)C
SMILES (Isomeric) CC(=O)O[C@]1(C(=O)C(=C)[C@@H]2[C@@]([C@@]13CC[C@@]4(O3)C[C@@H](OC4)OC)(CCCC2(C)C)C)C
InChI InChI=1S/C24H36O6/c1-15-18-20(3,4)9-8-10-21(18,5)24(22(6,19(15)26)29-16(2)25)12-11-23(30-24)13-17(27-7)28-14-23/h17-18H,1,8-14H2,2-7H3/t17-,18+,21+,22+,23-,24+/m1/s1
InChI Key MMHWBOSXIUOOSO-BDADTYDISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H36O6
Molecular Weight 420.50 g/mol
Exact Mass 420.25118886 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.96
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 163105058

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9882 98.82%
Caco-2 + 0.5868 58.68%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8148 81.48%
OATP2B1 inhibitior - 0.8624 86.24%
OATP1B1 inhibitior + 0.8051 80.51%
OATP1B3 inhibitior + 0.8904 89.04%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.6204 62.04%
P-glycoprotein inhibitior - 0.4414 44.14%
P-glycoprotein substrate - 0.6680 66.80%
CYP3A4 substrate + 0.6825 68.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8892 88.92%
CYP3A4 inhibition - 0.6147 61.47%
CYP2C9 inhibition - 0.7900 79.00%
CYP2C19 inhibition - 0.8198 81.98%
CYP2D6 inhibition - 0.9390 93.90%
CYP1A2 inhibition - 0.7678 76.78%
CYP2C8 inhibition + 0.4622 46.22%
CYP inhibitory promiscuity - 0.8754 87.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5148 51.48%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.7518 75.18%
Skin irritation - 0.6258 62.58%
Skin corrosion - 0.9285 92.85%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7124 71.24%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.6287 62.87%
skin sensitisation - 0.8070 80.70%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.6954 69.54%
Acute Oral Toxicity (c) III 0.4479 44.79%
Estrogen receptor binding + 0.8287 82.87%
Androgen receptor binding + 0.7207 72.07%
Thyroid receptor binding + 0.6663 66.63%
Glucocorticoid receptor binding + 0.7300 73.00%
Aromatase binding + 0.8116 81.16%
PPAR gamma + 0.6815 68.15%
Honey bee toxicity - 0.7112 71.12%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9953 99.53%

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 97.43% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.95% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.40% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.68% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.32% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.30% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.39% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.68% 97.25%
CHEMBL3922 P50579 Methionine aminopeptidase 2 86.68% 97.28%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.07% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.61% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.96% 92.94%
CHEMBL1951 P21397 Monoamine oxidase A 84.50% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.04% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.43% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.21% 91.19%
CHEMBL1937 Q92769 Histone deacetylase 2 82.55% 94.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.99% 92.62%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.56% 89.50%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.91% 95.71%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.03% 97.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.00% 100.00%

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.
Leonurus japonicus

Cross-Links

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PubChem 163105058
LOTUS LTS0046698
wikiData Q105167762