CID 162984526

Details

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Internal ID 7fc1af32-7dfb-4937-aad8-af1a1cb0ebb6
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name
SMILES (Canonical) CC1CC2C3C(CCCC3(C14CCC5(O4)CC(OC5=O)OC)C)(C(=O)O2)C
SMILES (Isomeric) C[C@H]1C[C@H]2[C@@H]3[C@@](CCC[C@]3([C@]14CC[C@@]5(O4)C[C@@H](OC5=O)OC)C)(C(=O)O2)C
InChI InChI=1S/C21H30O6/c1-12-10-13-15-18(2,16(22)25-13)6-5-7-19(15,3)21(12)9-8-20(27-21)11-14(24-4)26-17(20)23/h12-15H,5-11H2,1-4H3/t12-,13-,14+,15+,18+,19+,20+,21-/m0/s1
InChI Key NTKKRFQRYGKWKB-ABVYQAPASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H30O6
Molecular Weight 378.50 g/mol
Exact Mass 378.20423867 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 6
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 162984526

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9791 97.91%
Caco-2 + 0.6126 61.26%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7112 71.12%
OATP2B1 inhibitior - 0.8637 86.37%
OATP1B1 inhibitior + 0.8941 89.41%
OATP1B3 inhibitior + 0.9679 96.79%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6426 64.26%
P-glycoprotein inhibitior - 0.4893 48.93%
P-glycoprotein substrate - 0.6864 68.64%
CYP3A4 substrate + 0.6500 65.00%
CYP2C9 substrate - 0.8050 80.50%
CYP2D6 substrate - 0.8355 83.55%
CYP3A4 inhibition - 0.8232 82.32%
CYP2C9 inhibition - 0.9223 92.23%
CYP2C19 inhibition - 0.8879 88.79%
CYP2D6 inhibition - 0.9637 96.37%
CYP1A2 inhibition - 0.8150 81.50%
CYP2C8 inhibition - 0.6682 66.82%
CYP inhibitory promiscuity - 0.9587 95.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5540 55.40%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.8780 87.80%
Skin irritation - 0.6498 64.98%
Skin corrosion - 0.8002 80.02%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4804 48.04%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8988 89.88%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.7680 76.80%
Acute Oral Toxicity (c) III 0.4689 46.89%
Estrogen receptor binding + 0.8753 87.53%
Androgen receptor binding + 0.6999 69.99%
Thyroid receptor binding + 0.7210 72.10%
Glucocorticoid receptor binding + 0.8748 87.48%
Aromatase binding + 0.8594 85.94%
PPAR gamma + 0.7223 72.23%
Honey bee toxicity - 0.7619 76.19%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9615 96.15%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.46% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.13% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.07% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.01% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.73% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.38% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.01% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.33% 97.25%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.74% 97.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.50% 82.69%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.95% 95.71%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.01% 93.40%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.71% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.06% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 81.95% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.99% 86.33%

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.
Marrubium anisodon

Cross-Links

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PubChem 162984526
LOTUS LTS0163110
wikiData Q105185482