CID 163022189

Details

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Internal ID 6b8c4bf7-f824-4104-a4be-efb28873413f
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name
SMILES (Canonical) CC(C)C(=O)OC1CC2(C(C3C1(C4(CCC3)CO4)COC(=O)C)(C(CC5(O2)CC(=O)OC5)OC(=O)C)C)C
SMILES (Isomeric) CC(C)C(=O)OC1CC2(C(C3C1(C4(CCC3)CO4)COC(=O)C)(C(CC5(O2)CC(=O)OC5)OC(=O)C)C)C
InChI InChI=1S/C28H40O10/c1-16(2)23(32)37-21-10-24(5)25(6,20(36-18(4)30)11-26(38-24)12-22(31)34-13-26)19-8-7-9-27(14-35-27)28(19,21)15-33-17(3)29/h16,19-21H,7-15H2,1-6H3
InChI Key IDFGPSFGOXFUHL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H40O10
Molecular Weight 536.60 g/mol
Exact Mass 536.26214747 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 163022189

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9440 94.40%
Caco-2 - 0.6646 66.46%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8101 81.01%
OATP2B1 inhibitior - 0.8641 86.41%
OATP1B1 inhibitior + 0.8533 85.33%
OATP1B3 inhibitior + 0.9705 97.05%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.9045 90.45%
P-glycoprotein inhibitior + 0.7175 71.75%
P-glycoprotein substrate - 0.5503 55.03%
CYP3A4 substrate + 0.6778 67.78%
CYP2C9 substrate - 0.8095 80.95%
CYP2D6 substrate - 0.8590 85.90%
CYP3A4 inhibition - 0.8726 87.26%
CYP2C9 inhibition - 0.8062 80.62%
CYP2C19 inhibition - 0.7462 74.62%
CYP2D6 inhibition - 0.9345 93.45%
CYP1A2 inhibition - 0.8950 89.50%
CYP2C8 inhibition + 0.5681 56.81%
CYP inhibitory promiscuity - 0.9175 91.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5867 58.67%
Eye corrosion - 0.9839 98.39%
Eye irritation - 0.8592 85.92%
Skin irritation - 0.7557 75.57%
Skin corrosion - 0.9122 91.22%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4506 45.06%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5723 57.23%
skin sensitisation - 0.8553 85.53%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.7640 76.40%
Acute Oral Toxicity (c) III 0.4043 40.43%
Estrogen receptor binding + 0.8641 86.41%
Androgen receptor binding + 0.7235 72.35%
Thyroid receptor binding + 0.5804 58.04%
Glucocorticoid receptor binding + 0.8096 80.96%
Aromatase binding + 0.8005 80.05%
PPAR gamma + 0.7434 74.34%
Honey bee toxicity - 0.7354 73.54%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9668 96.68%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.81% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.78% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.17% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.13% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.16% 97.09%
CHEMBL2581 P07339 Cathepsin D 93.03% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.56% 97.25%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.55% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.33% 89.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.19% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.41% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.67% 95.89%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 87.45% 95.71%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 87.01% 89.05%
CHEMBL340 P08684 Cytochrome P450 3A4 86.89% 91.19%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.18% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.92% 99.23%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 85.36% 91.65%
CHEMBL2413 P32246 C-C chemokine receptor type 1 84.96% 89.50%
CHEMBL299 P17252 Protein kinase C alpha 84.76% 98.03%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.65% 94.80%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.46% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.69% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.22% 86.33%
CHEMBL5255 O00206 Toll-like receptor 4 81.66% 92.50%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.39% 95.17%

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.
Scutellaria orientalis

Cross-Links

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PubChem 163022189
LOTUS LTS0033156
wikiData Q105111315