CID 3036768

Details

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Internal ID 4144ddf0-d71f-437e-a823-081430b3a36c
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name
SMILES (Canonical) CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O
SMILES (Isomeric) C[C@@H]1C[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/C22H28O7/c1-13-8-18(24)22(12-27-14(2)23)17(4-3-6-20(22)11-28-20)21(13)9-16(29-19(21)25)15-5-7-26-10-15/h5,7,10,13,16-18,24H,3-4,6,8-9,11-12H2,1-2H3/t13-,16+,17-,18-,20+,21-,22+/m1/s1
InChI Key LOZYVHYKXUKJDA-RBANXJOPSA-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 3036768

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9806 98.06%
Caco-2 - 0.7068 70.68%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8440 84.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7731 77.31%
OATP1B3 inhibitior + 0.8949 89.49%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7287 72.87%
BSEP inhibitior - 0.6304 63.04%
P-glycoprotein inhibitior - 0.6004 60.04%
P-glycoprotein substrate - 0.6048 60.48%
CYP3A4 substrate + 0.6714 67.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8241 82.41%
CYP3A4 inhibition + 0.5374 53.74%
CYP2C9 inhibition - 0.6294 62.94%
CYP2C19 inhibition - 0.6905 69.05%
CYP2D6 inhibition - 0.9418 94.18%
CYP1A2 inhibition - 0.9112 91.12%
CYP2C8 inhibition + 0.5187 51.87%
CYP inhibitory promiscuity - 0.8908 89.08%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5458 54.58%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9368 93.68%
Skin irritation - 0.7193 71.93%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.6270 62.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8157 81.57%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.5932 59.32%
skin sensitisation - 0.9118 91.18%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.4534 45.34%
Acute Oral Toxicity (c) I 0.4346 43.46%
Estrogen receptor binding + 0.9216 92.16%
Androgen receptor binding + 0.6720 67.20%
Thyroid receptor binding - 0.4895 48.95%
Glucocorticoid receptor binding + 0.8135 81.35%
Aromatase binding + 0.7691 76.91%
PPAR gamma + 0.5268 52.68%
Honey bee toxicity - 0.8098 80.98%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9904 99.04%

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 96.65% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.15% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.86% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.68% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 92.49% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.21% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.46% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.30% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.18% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.68% 100.00%
CHEMBL2581 P07339 Cathepsin D 85.99% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.99% 94.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.79% 94.80%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.51% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.12% 95.56%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.95% 95.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.61% 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 corymbosum
Teucrium japonicum
Teucrium maghrebinum
Teucrium massiliense
Teucrium montanum
Teucrium polium

Cross-Links

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PubChem 3036768
LOTUS LTS0016381
wikiData Q104396020