Hypogeamicin B

Details

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Internal ID ffbe629f-25e4-4810-a841-6d278fcbb156
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name 2-[(1S,10R,11R,13S)-7-hydroxy-5-methoxy-2,9-dioxo-11-propyl-12,15-dioxatetracyclo[8.4.1.01,10.03,8]pentadeca-3(8),4,6-trien-13-yl]acetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H21NO7/c1-3-4-13-19-17(24)15-11(5-9(25-2)6-12(15)21)16(23)18(19,27-19)8-10(26-13)7-14(20)22/h5-6,10,13,21H,3-4,7-8H2,1-2H3,(H2,20,22)/t10-,13-,18-,19+/m1/s1
InChI Key BVHMHHVRJIFURL-YFTNOKGMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H21NO7
Molecular Weight 375.40 g/mol
Exact Mass 375.13180201 g/mol
Topological Polar Surface Area (TPSA) 128.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.12
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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CHEMBL3329781

2D Structure

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2D Structure of Hypogeamicin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9445 94.45%
Caco-2 + 0.5070 50.70%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5448 54.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8377 83.77%
OATP1B3 inhibitior + 0.9401 94.01%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8572 85.72%
BSEP inhibitior - 0.6609 66.09%
P-glycoprotein inhibitior - 0.5332 53.32%
P-glycoprotein substrate + 0.5754 57.54%
CYP3A4 substrate + 0.6193 61.93%
CYP2C9 substrate - 0.8018 80.18%
CYP2D6 substrate - 0.8407 84.07%
CYP3A4 inhibition - 0.8243 82.43%
CYP2C9 inhibition - 0.7969 79.69%
CYP2C19 inhibition - 0.7759 77.59%
CYP2D6 inhibition - 0.8611 86.11%
CYP1A2 inhibition - 0.7247 72.47%
CYP2C8 inhibition + 0.6079 60.79%
CYP inhibitory promiscuity - 0.8382 83.82%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5597 55.97%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.9096 90.96%
Skin irritation - 0.7798 77.98%
Skin corrosion - 0.9266 92.66%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4549 45.49%
Micronuclear + 0.6500 65.00%
Hepatotoxicity - 0.6528 65.28%
skin sensitisation - 0.8507 85.07%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6558 65.58%
Acute Oral Toxicity (c) III 0.5573 55.73%
Estrogen receptor binding + 0.8993 89.93%
Androgen receptor binding + 0.7150 71.50%
Thyroid receptor binding + 0.6011 60.11%
Glucocorticoid receptor binding + 0.8582 85.82%
Aromatase binding + 0.7038 70.38%
PPAR gamma + 0.7675 76.75%
Honey bee toxicity - 0.9059 90.59%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5432 54.32%
Fish aquatic toxicity - 0.6383 63.83%

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 99.41% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.53% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.65% 97.09%
CHEMBL4208 P20618 Proteasome component C5 93.79% 90.00%
CHEMBL2581 P07339 Cathepsin D 93.08% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.52% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.23% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.29% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 89.69% 91.07%
CHEMBL4581 P52732 Kinesin-like protein 1 88.46% 93.18%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.37% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.01% 89.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.68% 96.95%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 86.47% 92.68%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.32% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.12% 94.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.40% 96.21%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 84.36% 80.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.48% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.19% 92.94%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.52% 97.14%
CHEMBL226 P30542 Adenosine A1 receptor 82.02% 95.93%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.72% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.62% 99.23%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.61% 94.42%
CHEMBL4530 P00488 Coagulation factor XIII 80.09% 96.00%

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 118712552
LOTUS LTS0004527
wikiData Q75067731