Hypogeamicin C

Details

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Internal ID f6f2ee0c-223f-49ac-bd8e-379cc4188a3a
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones > Naphthopyranone glycosides
IUPAC Name 2-[(1R,3S,4aR,10aR)-4a,9,10a-trihydroxy-7-methoxy-5,10-dioxo-1-propyl-3,4-dihydro-1H-benzo[g]isochromen-3-yl]acetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H23NO8/c1-3-4-13-19(26)17(24)15-11(5-9(27-2)6-12(15)21)16(23)18(19,25)8-10(28-13)7-14(20)22/h5-6,10,13,21,25-26H,3-4,7-8H2,1-2H3,(H2,20,22)/t10-,13-,18+,19+/m1/s1
InChI Key PEEHMYIBRREDFW-OLNJAIPVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H23NO8
Molecular Weight 393.40 g/mol
Exact Mass 393.14236669 g/mol
Topological Polar Surface Area (TPSA) 156.00 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.07
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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CHEMBL3329782

2D Structure

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2D Structure of Hypogeamicin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9291 92.91%
Caco-2 - 0.6492 64.92%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6128 61.28%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9000 90.00%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9322 93.22%
BSEP inhibitior - 0.6894 68.94%
P-glycoprotein inhibitior - 0.6430 64.30%
P-glycoprotein substrate + 0.5050 50.50%
CYP3A4 substrate + 0.6079 60.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8489 84.89%
CYP3A4 inhibition - 0.8453 84.53%
CYP2C9 inhibition - 0.8514 85.14%
CYP2C19 inhibition - 0.8150 81.50%
CYP2D6 inhibition - 0.8878 88.78%
CYP1A2 inhibition - 0.6299 62.99%
CYP2C8 inhibition + 0.4867 48.67%
CYP inhibitory promiscuity - 0.9008 90.08%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5873 58.73%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.9253 92.53%
Skin irritation - 0.7817 78.17%
Skin corrosion - 0.9310 93.10%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5218 52.18%
Micronuclear + 0.6800 68.00%
Hepatotoxicity - 0.6067 60.67%
skin sensitisation - 0.8765 87.65%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.4585 45.85%
Acute Oral Toxicity (c) III 0.5418 54.18%
Estrogen receptor binding + 0.8483 84.83%
Androgen receptor binding + 0.6528 65.28%
Thyroid receptor binding + 0.5930 59.30%
Glucocorticoid receptor binding + 0.8382 83.82%
Aromatase binding + 0.7239 72.39%
PPAR gamma + 0.6946 69.46%
Honey bee toxicity - 0.9118 91.18%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5732 57.32%
Fish aquatic toxicity - 0.4637 46.37%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.45% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.36% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 96.50% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.56% 97.09%
CHEMBL4208 P20618 Proteasome component C5 94.97% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.41% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.84% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.84% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 90.48% 96.21%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.03% 92.94%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 89.42% 91.07%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.83% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.02% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.79% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.45% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.57% 94.00%
CHEMBL4581 P52732 Kinesin-like protein 1 85.39% 93.18%
CHEMBL340 P08684 Cytochrome P450 3A4 84.36% 91.19%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.21% 92.68%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 83.26% 80.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.96% 92.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.23% 96.95%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.93% 97.28%

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.
There are no matching plants.

Cross-Links

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PubChem 118712553
LOTUS LTS0257814
wikiData Q77421957