CID 101682668

Details

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Internal ID e672fc9d-0b5a-4968-b2fe-fbf383f93299
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name
SMILES (Canonical) CC1CC2C3C(CCCC3(C14CC(=O)C5(O4)COC=C5)C)(C(=O)O2)C
SMILES (Isomeric) C[C@@H]1C[C@@H]2C3[C@](CCC[C@@]3([C@@]14CC(=O)[C@]5(O4)COC=C5)C)(C(=O)O2)C
InChI InChI=1S/C20H26O5/c1-12-9-13-15-17(2,16(22)24-13)5-4-6-18(15,3)20(12)10-14(21)19(25-20)7-8-23-11-19/h7-8,12-13,15H,4-6,9-11H2,1-3H3/t12-,13-,15?,17+,18+,19-,20-/m1/s1
InChI Key JJFPECOASGDKQV-HPIZDLQCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H26O5
Molecular Weight 346.40 g/mol
Exact Mass 346.17802393 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 101682668

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.7075 70.75%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7714 77.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8885 88.85%
OATP1B3 inhibitior + 0.9578 95.78%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.6429 64.29%
P-glycoprotein inhibitior - 0.6107 61.07%
P-glycoprotein substrate - 0.6526 65.26%
CYP3A4 substrate + 0.6170 61.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8523 85.23%
CYP3A4 inhibition - 0.8157 81.57%
CYP2C9 inhibition - 0.9378 93.78%
CYP2C19 inhibition - 0.9247 92.47%
CYP2D6 inhibition - 0.9626 96.26%
CYP1A2 inhibition - 0.8397 83.97%
CYP2C8 inhibition - 0.5998 59.98%
CYP inhibitory promiscuity - 0.9470 94.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4839 48.39%
Eye corrosion - 0.9860 98.60%
Eye irritation - 0.9705 97.05%
Skin irritation - 0.5441 54.41%
Skin corrosion - 0.8559 85.59%
Ames mutagenesis + 0.5430 54.30%
Human Ether-a-go-go-Related Gene inhibition + 0.6671 66.71%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6282 62.82%
skin sensitisation - 0.8900 89.00%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.8836 88.36%
Acute Oral Toxicity (c) III 0.5900 59.00%
Estrogen receptor binding + 0.8676 86.76%
Androgen receptor binding + 0.7047 70.47%
Thyroid receptor binding + 0.7380 73.80%
Glucocorticoid receptor binding + 0.8059 80.59%
Aromatase binding + 0.8174 81.74%
PPAR gamma + 0.6691 66.91%
Honey bee toxicity - 0.8054 80.54%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9891 98.91%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.57% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.15% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.93% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.16% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.71% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.41% 82.69%
CHEMBL230 P35354 Cyclooxygenase-2 89.29% 89.63%
CHEMBL1937 Q92769 Histone deacetylase 2 89.13% 94.75%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.62% 93.40%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.00% 96.09%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 86.70% 95.71%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.69% 85.30%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.50% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.87% 86.33%
CHEMBL2996 Q05655 Protein kinase C delta 84.69% 97.79%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.75% 93.04%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.37% 85.14%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.78% 86.00%
CHEMBL325 Q13547 Histone deacetylase 1 81.20% 95.92%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.95% 92.94%

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 astracanicum
Marrubium globosum

Cross-Links

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PubChem 101682668
LOTUS LTS0006892
wikiData Q105129629