CID 102054462

Details

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Internal ID e25c54d4-84e2-499f-a291-d9158c85ade7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name
SMILES (Canonical) CC(=O)OC1CCC2(C(C1(C)C)CC(=O)C(C23CCC4(O3)CC(OC4)OC)(C)OC(=O)C)C
SMILES (Isomeric) CC(=O)O[C@@H]1CC[C@]2([C@H](C1(C)C)CC(=O)[C@]([C@@]23CC[C@@]4(O3)C[C@@H](OC4)OC)(C)OC(=O)C)C
InChI InChI=1S/C25H38O8/c1-15(26)31-19-8-9-22(5)17(21(19,3)4)12-18(28)23(6,32-16(2)27)25(22)11-10-24(33-25)13-20(29-7)30-14-24/h17,19-20H,8-14H2,1-7H3/t17-,19+,20+,22-,23-,24+,25+/m0/s1
InChI Key LKSFITIHGZYUMQ-CWAWTUSFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H38O8
Molecular Weight 466.60 g/mol
Exact Mass 466.25666817 g/mol
Topological Polar Surface Area (TPSA) 97.40 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 102054462

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9797 97.97%
Caco-2 - 0.5734 57.34%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8127 81.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8123 81.23%
OATP1B3 inhibitior + 0.9780 97.80%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.7956 79.56%
P-glycoprotein inhibitior + 0.6755 67.55%
P-glycoprotein substrate - 0.6639 66.39%
CYP3A4 substrate + 0.6879 68.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8779 87.79%
CYP3A4 inhibition - 0.7934 79.34%
CYP2C9 inhibition - 0.7977 79.77%
CYP2C19 inhibition - 0.8275 82.75%
CYP2D6 inhibition - 0.9513 95.13%
CYP1A2 inhibition - 0.9111 91.11%
CYP2C8 inhibition + 0.5894 58.94%
CYP inhibitory promiscuity - 0.9446 94.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5560 55.60%
Eye corrosion - 0.9848 98.48%
Eye irritation - 0.8077 80.77%
Skin irritation - 0.7741 77.41%
Skin corrosion - 0.9126 91.26%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3913 39.13%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.6468 64.68%
skin sensitisation - 0.8863 88.63%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.8038 80.38%
Acute Oral Toxicity (c) III 0.5256 52.56%
Estrogen receptor binding + 0.8970 89.70%
Androgen receptor binding + 0.7375 73.75%
Thyroid receptor binding + 0.6638 66.38%
Glucocorticoid receptor binding + 0.7689 76.89%
Aromatase binding + 0.8254 82.54%
PPAR gamma + 0.7214 72.14%
Honey bee toxicity - 0.7418 74.18%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9685 96.85%

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 96.31% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.83% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.26% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 92.14% 92.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.57% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.75% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.06% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.40% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.64% 92.62%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.47% 93.03%
CHEMBL340 P08684 Cytochrome P450 3A4 85.95% 91.19%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.76% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.90% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.29% 100.00%
CHEMBL2581 P07339 Cathepsin D 83.99% 98.95%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 83.42% 96.39%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.24% 93.04%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.70% 95.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.63% 97.14%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 81.53% 98.99%
CHEMBL1937 Q92769 Histone deacetylase 2 81.31% 94.75%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.77% 97.28%

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 sibiricus

Cross-Links

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PubChem 102054462
LOTUS LTS0103151
wikiData Q105153252