CID 163014799

Details

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Internal ID 73b2dfe6-dcb9-4017-953f-81aa33096379
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H32O5/c1-13-10-14-16-18(2,17(22)25-14)6-5-7-19(16,3)21(13)9-8-20(26-21)11-15(23-4)24-12-20/h13-16H,5-12H2,1-4H3/t13-,14-,15+,16+,18+,19+,20+,21-/m1/s1
InChI Key QBCPPXUWUDONEX-SEPVDIHQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O5
Molecular Weight 364.50 g/mol
Exact Mass 364.22497412 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.45
H-Bond Acceptor 5
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 163014799

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 + 0.6417 64.17%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7145 71.45%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.8839 88.39%
OATP1B3 inhibitior + 0.9769 97.69%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.4910 49.10%
P-glycoprotein inhibitior - 0.6570 65.70%
P-glycoprotein substrate - 0.6411 64.11%
CYP3A4 substrate + 0.6660 66.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8548 85.48%
CYP3A4 inhibition - 0.8295 82.95%
CYP2C9 inhibition - 0.8698 86.98%
CYP2C19 inhibition - 0.8340 83.40%
CYP2D6 inhibition - 0.9460 94.60%
CYP1A2 inhibition - 0.8605 86.05%
CYP2C8 inhibition - 0.5712 57.12%
CYP inhibitory promiscuity - 0.9198 91.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5610 56.10%
Eye corrosion - 0.9855 98.55%
Eye irritation - 0.8831 88.31%
Skin irritation - 0.7457 74.57%
Skin corrosion - 0.9395 93.95%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4687 46.87%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.9072 90.72%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.7603 76.03%
Acute Oral Toxicity (c) III 0.4575 45.75%
Estrogen receptor binding + 0.8738 87.38%
Androgen receptor binding + 0.6960 69.60%
Thyroid receptor binding + 0.7097 70.97%
Glucocorticoid receptor binding + 0.8097 80.97%
Aromatase binding + 0.8659 86.59%
PPAR gamma + 0.7077 70.77%
Honey bee toxicity - 0.7014 70.14%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9376 93.76%

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 92.40% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.12% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.06% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.55% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.21% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.05% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.78% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.84% 82.69%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 87.15% 95.71%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.39% 92.94%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.49% 85.14%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.19% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.17% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.50% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 82.35% 97.79%
CHEMBL240 Q12809 HERG 81.66% 89.76%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.55% 94.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.36% 91.07%
CHEMBL1937 Q92769 Histone deacetylase 2 80.17% 94.75%

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 cylleneum

Cross-Links

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PubChem 163014799
LOTUS LTS0130013
wikiData Q105217730