CID 14163581

Details

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Internal ID f4b1f39b-cee2-480b-abe8-0f7ac5f8439a
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name
SMILES (Canonical) CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)CO)OC(=O)C
SMILES (Isomeric) C[C@@H]1C[C@@H]([C@@]2([C@@H]([C@@]13C[C@@H](OC3=O)C4=COC=C4)CCC[C@]25CO5)CO)OC(=O)C
InChI InChI=1S/C22H28O7/c1-13-8-18(28-14(2)24)22(11-23)17(4-3-6-20(22)12-27-20)21(13)9-16(29-19(21)25)15-5-7-26-10-15/h5,7,10,13,16-18,23H,3-4,6,8-9,11-12H2,1-2H3/t13-,16-,17-,18+,20+,21-,22+/m1/s1
InChI Key VBPDFHXDMUNMDH-GOORKCOQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28O7
Molecular Weight 404.50 g/mol
Exact Mass 404.18350323 g/mol
Topological Polar Surface Area (TPSA) 98.50 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.77
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 14163581

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9555 95.55%
Caco-2 - 0.6883 68.83%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8202 82.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7597 75.97%
OATP1B3 inhibitior + 0.9162 91.62%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.5334 53.34%
P-glycoprotein inhibitior - 0.6314 63.14%
P-glycoprotein substrate - 0.6486 64.86%
CYP3A4 substrate + 0.6788 67.88%
CYP2C9 substrate - 0.8018 80.18%
CYP2D6 substrate - 0.8384 83.84%
CYP3A4 inhibition + 0.5905 59.05%
CYP2C9 inhibition - 0.6977 69.77%
CYP2C19 inhibition - 0.7384 73.84%
CYP2D6 inhibition - 0.9352 93.52%
CYP1A2 inhibition - 0.8864 88.64%
CYP2C8 inhibition + 0.5591 55.91%
CYP inhibitory promiscuity - 0.7927 79.27%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5402 54.02%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9391 93.91%
Skin irritation - 0.7299 72.99%
Skin corrosion - 0.9366 93.66%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8124 81.24%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.6192 61.92%
skin sensitisation - 0.9110 91.10%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5864 58.64%
Acute Oral Toxicity (c) I 0.3596 35.96%
Estrogen receptor binding + 0.9188 91.88%
Androgen receptor binding + 0.6499 64.99%
Thyroid receptor binding + 0.5365 53.65%
Glucocorticoid receptor binding + 0.8050 80.50%
Aromatase binding + 0.7334 73.34%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.8275 82.75%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9865 98.65%

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 96.96% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.42% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.64% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 93.27% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.25% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.45% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.55% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.78% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.16% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.63% 94.80%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.57% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.09% 95.56%
CHEMBL2581 P07339 Cathepsin D 83.57% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.32% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.29% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.05% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 82.64% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.34% 95.89%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.60% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 81.48% 92.50%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.41% 82.69%

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.
Teucrium abutiloides
Teucrium canadense
Teucrium lamiifolium

Cross-Links

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PubChem 14163581
LOTUS LTS0250355
wikiData Q104396013