CID 101528285

Details

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Internal ID da4dc2f3-8924-426a-84b2-a3efe4bd3697
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name
SMILES (Canonical) CC1C(=O)C(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O
SMILES (Isomeric) C[C@@H]1C(=O)[C@@H]([C@@]2([C@@H]([C@@]13C[C@H](OC3=O)C4=COC=C4)CCC[C@]25CO5)COC(=O)C)O
InChI InChI=1S/C22H26O8/c1-12-17(24)18(25)22(11-28-13(2)23)16(4-3-6-20(22)10-29-20)21(12)8-15(30-19(21)26)14-5-7-27-9-14/h5,7,9,12,15-16,18,25H,3-4,6,8,10-11H2,1-2H3/t12-,15+,16-,18+,20+,21-,22+/m1/s1
InChI Key LIBVFFSKNVMDTN-YLEXFDPASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O8
Molecular Weight 418.40 g/mol
Exact Mass 418.16276778 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.95
H-Bond Acceptor 8
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 101528285

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9613 96.13%
Caco-2 - 0.7183 71.83%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8867 88.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7563 75.63%
OATP1B3 inhibitior + 0.8959 89.59%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7287 72.87%
BSEP inhibitior + 0.6946 69.46%
P-glycoprotein inhibitior - 0.4479 44.79%
P-glycoprotein substrate - 0.6247 62.47%
CYP3A4 substrate + 0.6544 65.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8268 82.68%
CYP3A4 inhibition - 0.6459 64.59%
CYP2C9 inhibition - 0.6364 63.64%
CYP2C19 inhibition - 0.6666 66.66%
CYP2D6 inhibition - 0.9512 95.12%
CYP1A2 inhibition - 0.8969 89.69%
CYP2C8 inhibition + 0.5119 51.19%
CYP inhibitory promiscuity - 0.8259 82.59%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5419 54.19%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.9145 91.45%
Skin irritation - 0.7589 75.89%
Skin corrosion - 0.9394 93.94%
Ames mutagenesis - 0.6970 69.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8535 85.35%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.6361 63.61%
skin sensitisation - 0.8982 89.82%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.6417 64.17%
Acute Oral Toxicity (c) I 0.3932 39.32%
Estrogen receptor binding + 0.9124 91.24%
Androgen receptor binding + 0.7035 70.35%
Thyroid receptor binding + 0.5368 53.68%
Glucocorticoid receptor binding + 0.7956 79.56%
Aromatase binding + 0.7284 72.84%
PPAR gamma + 0.5755 57.55%
Honey bee toxicity - 0.8270 82.70%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5050 50.50%
Fish aquatic toxicity + 0.9821 98.21%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 96.15% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.96% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.61% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.40% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.22% 85.14%
CHEMBL221 P23219 Cyclooxygenase-1 91.59% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.43% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.73% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.67% 89.00%
CHEMBL2581 P07339 Cathepsin D 86.61% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.58% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.19% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.48% 94.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.25% 94.80%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.07% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.69% 92.62%

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 polium

Cross-Links

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PubChem 101528285
LOTUS LTS0219188
wikiData Q105152108