CID 85283951

Details

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Internal ID 6982aac9-7005-4b2f-ada0-d45ed31f0099
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Abscisic acids and derivatives
IUPAC Name
SMILES (Canonical) CC(=O)OC1(C(=O)C2C3C(CCCC3(C14CCC5(O4)CC(=O)OC5)C)(C(=O)O2)C)C
SMILES (Isomeric) CC(=O)OC1(C(=O)C2C3C(CCCC3(C14CCC5(O4)CC(=O)OC5)C)(C(=O)O2)C)C
InChI InChI=1S/C22H28O8/c1-12(23)29-20(4)16(25)14-15-18(2,17(26)28-14)6-5-7-19(15,3)22(20)9-8-21(30-22)10-13(24)27-11-21/h14-15H,5-11H2,1-4H3
InChI Key VCBMKVRJLRIJHA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28O8
Molecular Weight 420.50 g/mol
Exact Mass 420.17841785 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.86
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 85283951

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9819 98.19%
Caco-2 + 0.5115 51.15%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7880 78.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8706 87.06%
OATP1B3 inhibitior + 0.9687 96.87%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.8016 80.16%
P-glycoprotein inhibitior + 0.6833 68.33%
P-glycoprotein substrate - 0.6952 69.52%
CYP3A4 substrate + 0.6460 64.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8579 85.79%
CYP3A4 inhibition - 0.8521 85.21%
CYP2C9 inhibition - 0.8803 88.03%
CYP2C19 inhibition - 0.8735 87.35%
CYP2D6 inhibition - 0.9623 96.23%
CYP1A2 inhibition - 0.8717 87.17%
CYP2C8 inhibition - 0.5954 59.54%
CYP inhibitory promiscuity - 0.9347 93.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5521 55.21%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.8277 82.77%
Skin irritation - 0.6779 67.79%
Skin corrosion - 0.8819 88.19%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6571 65.71%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation - 0.9197 91.97%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.7663 76.63%
Acute Oral Toxicity (c) III 0.5420 54.20%
Estrogen receptor binding + 0.8620 86.20%
Androgen receptor binding + 0.7066 70.66%
Thyroid receptor binding + 0.6662 66.62%
Glucocorticoid receptor binding + 0.7897 78.97%
Aromatase binding + 0.7663 76.63%
PPAR gamma + 0.5684 56.84%
Honey bee toxicity - 0.8151 81.51%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6750 67.50%
Fish aquatic toxicity + 0.9783 97.83%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.36% 85.14%
CHEMBL2581 P07339 Cathepsin D 93.44% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.41% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.59% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.42% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.47% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.56% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.41% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.21% 89.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.30% 82.69%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.40% 97.25%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.81% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.95% 97.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.48% 93.04%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.29% 97.14%
CHEMBL5028 O14672 ADAM10 81.04% 97.50%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.34% 95.71%

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 persicus

Cross-Links

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PubChem 85283951
LOTUS LTS0071244
wikiData Q105283593