CID 102000285

Details

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Internal ID 485f1f04-7be2-4cbf-bf67-39285421fde1
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name
SMILES (Canonical) CC1CC(=O)C2(C(C13CC(OC3O)C4=COC=C4)CCCC25CO5)COC(=O)C
SMILES (Isomeric) C[C@@H]1CC(=O)[C@@]2([C@@H]([C@@]13C[C@H](O[C@@H]3O)C4=COC=C4)CCC[C@]25CO5)COC(=O)C
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/h5,7,10,13,16-17,19,25H,3-4,6,8-9,11-12H2,1-2H3/t13-,16+,17-,19+,20+,21-,22+/m1/s1
InChI Key NUWZPFWRHBOHLZ-LKFGLWOWSA-N
Popularity 2 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 1.20
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 102000285

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9733 97.33%
Caco-2 - 0.6310 63.10%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8679 86.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7763 77.63%
OATP1B3 inhibitior + 0.8971 89.71%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7287 72.87%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.5892 58.92%
P-glycoprotein substrate - 0.5898 58.98%
CYP3A4 substrate + 0.6538 65.38%
CYP2C9 substrate - 0.6060 60.60%
CYP2D6 substrate - 0.8472 84.72%
CYP3A4 inhibition - 0.5837 58.37%
CYP2C9 inhibition - 0.5989 59.89%
CYP2C19 inhibition - 0.6694 66.94%
CYP2D6 inhibition - 0.9444 94.44%
CYP1A2 inhibition - 0.8943 89.43%
CYP2C8 inhibition + 0.5422 54.22%
CYP inhibitory promiscuity - 0.8340 83.40%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5550 55.50%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9558 95.58%
Skin irritation - 0.7519 75.19%
Skin corrosion - 0.9376 93.76%
Ames mutagenesis - 0.5670 56.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7406 74.06%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.5056 50.56%
skin sensitisation - 0.9138 91.38%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6408 64.08%
Acute Oral Toxicity (c) I 0.4126 41.26%
Estrogen receptor binding + 0.8882 88.82%
Androgen receptor binding + 0.7403 74.03%
Thyroid receptor binding - 0.5178 51.78%
Glucocorticoid receptor binding + 0.7778 77.78%
Aromatase binding + 0.7173 71.73%
PPAR gamma - 0.5543 55.43%
Honey bee toxicity - 0.8448 84.48%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5650 56.50%
Fish aquatic toxicity + 0.9936 99.36%

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 97.56% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.51% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.41% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.79% 97.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.11% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.74% 85.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.44% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.57% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.39% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.13% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.07% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.88% 86.33%
CHEMBL4040 P28482 MAP kinase ERK2 86.34% 83.82%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 85.67% 96.39%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.04% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.04% 89.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.79% 95.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.68% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.30% 95.56%

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 asiaticum

Cross-Links

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PubChem 102000285
LOTUS LTS0222382
wikiData Q105186058