CID 163001010

Details

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Internal ID 40732714-03ed-40c8-b997-00f338caf7d1
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name
SMILES (Canonical) CC(=O)OC1CC2C(=O)C3(CC(OC3=O)C4=COC=C4)C(CC2(C(=C)C15CO5)O)(C)O
SMILES (Isomeric) CC(=O)O[C@H]1C[C@H]2C(=O)[C@@]3(C[C@H](OC3=O)C4=COC=C4)[C@@](C[C@@]2(C(=C)[C@@]15CO5)O)(C)O
InChI InChI=1S/C22H24O9/c1-11-21(27)9-19(3,26)20(7-15(31-18(20)25)13-4-5-28-8-13)17(24)14(21)6-16(30-12(2)23)22(11)10-29-22/h4-5,8,14-16,26-27H,1,6-7,9-10H2,2-3H3/t14-,15-,16-,19-,20+,21-,22-/m0/s1
InChI Key FLKWQALNPWZBQI-GDDIOVTOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O9
Molecular Weight 432.40 g/mol
Exact Mass 432.14203234 g/mol
Topological Polar Surface Area (TPSA) 136.00 Ų
XlogP -0.90
Atomic LogP (AlogP) 0.99
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 163001010

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9747 97.47%
Caco-2 - 0.7709 77.09%
Blood Brain Barrier + 0.6027 60.27%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7332 73.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7384 73.84%
OATP1B3 inhibitior + 0.9458 94.58%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9614 96.14%
BSEP inhibitior - 0.5221 52.21%
P-glycoprotein inhibitior - 0.4934 49.34%
P-glycoprotein substrate - 0.5708 57.08%
CYP3A4 substrate + 0.6971 69.71%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8525 85.25%
CYP3A4 inhibition + 0.5075 50.75%
CYP2C9 inhibition - 0.7614 76.14%
CYP2C19 inhibition - 0.8497 84.97%
CYP2D6 inhibition - 0.9222 92.22%
CYP1A2 inhibition - 0.8584 85.84%
CYP2C8 inhibition + 0.4626 46.26%
CYP inhibitory promiscuity - 0.8083 80.83%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5455 54.55%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9216 92.16%
Skin irritation - 0.6473 64.73%
Skin corrosion - 0.9329 93.29%
Ames mutagenesis + 0.5163 51.63%
Human Ether-a-go-go-Related Gene inhibition - 0.5646 56.46%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.8270 82.70%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.7819 78.19%
Acute Oral Toxicity (c) I 0.5648 56.48%
Estrogen receptor binding + 0.8411 84.11%
Androgen receptor binding + 0.7498 74.98%
Thyroid receptor binding + 0.6421 64.21%
Glucocorticoid receptor binding + 0.7991 79.91%
Aromatase binding + 0.7595 75.95%
PPAR gamma + 0.5995 59.95%
Honey bee toxicity - 0.7689 76.89%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.46% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.09% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.77% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.46% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.26% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.61% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.18% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.83% 86.33%
CHEMBL4208 P20618 Proteasome component C5 85.94% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.93% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 84.22% 90.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.35% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.31% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.31% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 82.01% 91.19%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.04% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.59% 95.89%

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 brevifolium

Cross-Links

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PubChem 163001010
LOTUS LTS0183195
wikiData Q104997198