3'-Hydroxy-5,7-dimethoxy-4-O-2'-cycloflavan

Details

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Internal ID 927b3179-5f62-4a10-b960-3cf5d5684f6b
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans
IUPAC Name (1S,9S)-11,13-dimethoxy-8,16-dioxatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10(15),11,13-hexaen-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O5/c1-19-9-6-13(20-2)16-14(7-9)21-12-8-15(16)22-17-10(12)4-3-5-11(17)18/h3-7,12,15,18H,8H2,1-2H3/t12-,15-/m0/s1
InChI Key PJAWURWFLOLDDW-WFASDCNBSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O5
Molecular Weight 300.30 g/mol
Exact Mass 300.09977361 g/mol
Topological Polar Surface Area (TPSA) 57.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.37
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3'-Hydroxy-5,7-dimethoxy-4-O-2'-cycloflavan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9721 97.21%
Caco-2 + 0.7235 72.35%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6755 67.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9305 93.05%
OATP1B3 inhibitior + 0.9773 97.73%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6420 64.20%
P-glycoprotein inhibitior - 0.7571 75.71%
P-glycoprotein substrate - 0.7848 78.48%
CYP3A4 substrate + 0.5874 58.74%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate + 0.6029 60.29%
CYP3A4 inhibition - 0.6006 60.06%
CYP2C9 inhibition - 0.9225 92.25%
CYP2C19 inhibition + 0.6590 65.90%
CYP2D6 inhibition - 0.5246 52.46%
CYP1A2 inhibition + 0.8450 84.50%
CYP2C8 inhibition + 0.5811 58.11%
CYP inhibitory promiscuity - 0.6104 61.04%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5704 57.04%
Eye corrosion - 0.9757 97.57%
Eye irritation - 0.6458 64.58%
Skin irritation - 0.6929 69.29%
Skin corrosion - 0.9785 97.85%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4393 43.93%
Micronuclear + 0.7359 73.59%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8170 81.70%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6709 67.09%
Acute Oral Toxicity (c) III 0.6147 61.47%
Estrogen receptor binding + 0.7007 70.07%
Androgen receptor binding + 0.5892 58.92%
Thyroid receptor binding + 0.7569 75.69%
Glucocorticoid receptor binding + 0.6555 65.55%
Aromatase binding - 0.6444 64.44%
PPAR gamma + 0.6900 69.00%
Honey bee toxicity - 0.8724 87.24%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6851 68.51%
Fish aquatic toxicity - 0.5489 54.89%

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 96.94% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.84% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.83% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.70% 93.99%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.54% 97.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.05% 99.15%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.17% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.29% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.21% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.76% 86.33%
CHEMBL2535 P11166 Glucose transporter 86.36% 98.75%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 84.04% 89.32%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.00% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.97% 94.00%
CHEMBL4208 P20618 Proteasome component C5 83.89% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.53% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.56% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.09% 85.14%
CHEMBL2581 P07339 Cathepsin D 80.59% 98.95%

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.
Iris tenuifolia

Cross-Links

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PubChem 46847424
LOTUS LTS0017893
wikiData Q105209840