Phochrodine C

Details

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Internal ID f0da94bb-c40d-414f-a757-7625d8be158c
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromenopyridines
IUPAC Name 8-methoxy-2-methyl-5H-chromeno[4,3-b]pyridine-10-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H13NO4/c1-8-3-4-9-7-20-12-6-10(19-2)5-11(15(17)18)13(12)14(9)16-8/h3-6H,7H2,1-2H3,(H,17,18)
InChI Key CYRPVVBDNZXRMF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H13NO4
Molecular Weight 271.27 g/mol
Exact Mass 271.08445790 g/mol
Topological Polar Surface Area (TPSA) 68.70 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 4
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 Phochrodine C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9796 97.96%
Caco-2 + 0.6454 64.54%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7174 71.74%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9374 93.74%
OATP1B3 inhibitior + 0.9521 95.21%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5692 56.92%
P-glycoprotein inhibitior - 0.9011 90.11%
P-glycoprotein substrate - 0.8462 84.62%
CYP3A4 substrate - 0.5464 54.64%
CYP2C9 substrate - 0.8132 81.32%
CYP2D6 substrate - 0.8889 88.89%
CYP3A4 inhibition - 0.5955 59.55%
CYP2C9 inhibition - 0.8696 86.96%
CYP2C19 inhibition - 0.5900 59.00%
CYP2D6 inhibition - 0.8335 83.35%
CYP1A2 inhibition + 0.6228 62.28%
CYP2C8 inhibition - 0.6865 68.65%
CYP inhibitory promiscuity - 0.7185 71.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6232 62.32%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.8351 83.51%
Skin corrosion - 0.9841 98.41%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5720 57.20%
Micronuclear + 0.7374 73.74%
Hepatotoxicity + 0.5733 57.33%
skin sensitisation - 0.9006 90.06%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.4665 46.65%
Acute Oral Toxicity (c) III 0.6569 65.69%
Estrogen receptor binding + 0.7221 72.21%
Androgen receptor binding + 0.7651 76.51%
Thyroid receptor binding + 0.7143 71.43%
Glucocorticoid receptor binding + 0.9334 93.34%
Aromatase binding + 0.6547 65.47%
PPAR gamma + 0.8720 87.20%
Honey bee toxicity - 0.9334 93.34%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity - 0.5235 52.35%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.15% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.71% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.97% 96.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 88.73% 97.36%
CHEMBL2243 O00519 Anandamide amidohydrolase 88.72% 97.53%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.59% 81.11%
CHEMBL2047 Q96RI1 Bile acid receptor FXR 88.54% 96.10%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.99% 99.23%
CHEMBL4208 P20618 Proteasome component C5 87.25% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.87% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.31% 91.11%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.12% 93.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.41% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.37% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.98% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.56% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 83.24% 94.73%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.96% 96.67%

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 146684263
LOTUS LTS0049453
wikiData Q104972516