(3,4,5-Trihydroxy-6-methyloxan-2-yl) 6-(3-methylbut-2-enyl)phenazine-1-carboxylate

Details

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Internal ID 57477f8e-37bd-4b74-8d3c-04094806eb1e
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name (3,4,5-trihydroxy-6-methyloxan-2-yl) 6-(3-methylbut-2-enyl)phenazine-1-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H26N2O6/c1-12(2)10-11-14-6-4-8-16-18(14)25-17-9-5-7-15(19(17)26-16)23(30)32-24-22(29)21(28)20(27)13(3)31-24/h4-10,13,20-22,24,27-29H,11H2,1-3H3
InChI Key YYAZCIFRQFQQRH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26N2O6
Molecular Weight 438.50 g/mol
Exact Mass 438.17908655 g/mol
Topological Polar Surface Area (TPSA) 122.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3,4,5-Trihydroxy-6-methyloxan-2-yl) 6-(3-methylbut-2-enyl)phenazine-1-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8966 89.66%
Caco-2 - 0.7698 76.98%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.4473 44.73%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.9343 93.43%
OATP1B3 inhibitior + 0.9128 91.28%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8997 89.97%
P-glycoprotein inhibitior + 0.6014 60.14%
P-glycoprotein substrate - 0.7902 79.02%
CYP3A4 substrate + 0.5603 56.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8611 86.11%
CYP3A4 inhibition - 0.8880 88.80%
CYP2C9 inhibition - 0.8303 83.03%
CYP2C19 inhibition - 0.7014 70.14%
CYP2D6 inhibition - 0.8387 83.87%
CYP1A2 inhibition - 0.6225 62.25%
CYP2C8 inhibition + 0.5120 51.20%
CYP inhibitory promiscuity - 0.5696 56.96%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4979 49.79%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9390 93.90%
Skin irritation - 0.7769 77.69%
Skin corrosion - 0.9504 95.04%
Ames mutagenesis + 0.5046 50.46%
Human Ether-a-go-go-Related Gene inhibition - 0.5163 51.63%
Micronuclear + 0.6800 68.00%
Hepatotoxicity - 0.5233 52.33%
skin sensitisation - 0.8283 82.83%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6659 66.59%
Acute Oral Toxicity (c) III 0.6163 61.63%
Estrogen receptor binding + 0.8182 81.82%
Androgen receptor binding + 0.5242 52.42%
Thyroid receptor binding + 0.6317 63.17%
Glucocorticoid receptor binding + 0.8428 84.28%
Aromatase binding + 0.6754 67.54%
PPAR gamma + 0.7680 76.80%
Honey bee toxicity - 0.8739 87.39%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9273 92.73%

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
CHEMBL3401 O75469 Pregnane X receptor 98.32% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.57% 86.33%
CHEMBL2581 P07339 Cathepsin D 95.60% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.48% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.69% 96.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 93.60% 97.36%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.67% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.12% 94.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.30% 81.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.59% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.11% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.67% 96.00%
CHEMBL2096618 P11274 Bcr/Abl fusion protein 82.66% 85.83%
CHEMBL1951 P21397 Monoamine oxidase A 82.62% 91.49%
CHEMBL3891 P07384 Calpain 1 82.16% 93.04%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 81.72% 83.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 9845981
LOTUS LTS0182285
wikiData Q104202182