7-Oxohernangerine

Details

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Internal ID a1f8f9c5-baa0-4a79-8d61-e7442692cd4f
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 17-hydroxy-18-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,9,11,14(19),15,17-octaen-13-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H11NO5/c1-22-17-10(20)3-2-9-13(17)14-12-8(4-5-19-15(12)16(9)21)6-11-18(14)24-7-23-11/h2-6,20H,7H2,1H3
InChI Key IVWNIIWOWTWWKH-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C18H11NO5
Molecular Weight 321.30 g/mol
Exact Mass 321.06372245 g/mol
Topological Polar Surface Area (TPSA) 77.90 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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11-hydroxy-12-methoxy-8H-[1,3]benzodioxolo[6,5,4-de]benzo[g]quinolin-8-one
7-Oxahernangerine
CHEBI:66841
Q27135475
8H-1,3-benzodioxolo[6,5,4-de]benzo[g]quinolin-8-one, 11-hydroxy-12-methoxy-
17-hydroxy-18-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,9,11,14(19),15,17-octaen-13-one

2D Structure

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2D Structure of 7-Oxohernangerine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 + 0.6474 64.74%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6794 67.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9421 94.21%
OATP1B3 inhibitior + 0.9647 96.47%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6211 62.11%
P-glycoprotein inhibitior - 0.7687 76.87%
P-glycoprotein substrate - 0.8197 81.97%
CYP3A4 substrate + 0.5730 57.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7838 78.38%
CYP3A4 inhibition + 0.8390 83.90%
CYP2C9 inhibition - 0.6230 62.30%
CYP2C19 inhibition + 0.6029 60.29%
CYP2D6 inhibition - 0.6254 62.54%
CYP1A2 inhibition + 0.8549 85.49%
CYP2C8 inhibition + 0.5179 51.79%
CYP inhibitory promiscuity + 0.7911 79.11%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5246 52.46%
Eye corrosion - 0.9900 99.00%
Eye irritation + 0.6494 64.94%
Skin irritation - 0.7793 77.93%
Skin corrosion - 0.9637 96.37%
Ames mutagenesis + 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7690 76.90%
Micronuclear + 0.7874 78.74%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8378 83.78%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5395 53.95%
Acute Oral Toxicity (c) III 0.7130 71.30%
Estrogen receptor binding + 0.9247 92.47%
Androgen receptor binding - 0.4815 48.15%
Thyroid receptor binding + 0.6667 66.67%
Glucocorticoid receptor binding + 0.9420 94.20%
Aromatase binding + 0.7158 71.58%
PPAR gamma + 0.8412 84.12%
Honey bee toxicity - 0.8479 84.79%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity - 0.4760 47.60%

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 98.34% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.98% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.42% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.94% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.78% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.03% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.25% 86.33%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 92.82% 82.67%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 92.68% 96.67%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 92.23% 93.10%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.61% 99.23%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 91.04% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.30% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.06% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.34% 94.73%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 86.06% 96.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.93% 85.14%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.75% 94.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.12% 95.56%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 83.89% 92.68%
CHEMBL2535 P11166 Glucose transporter 83.50% 98.75%
CHEMBL1937 Q92769 Histone deacetylase 2 83.35% 94.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.08% 96.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.03% 100.00%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.74% 80.96%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.09% 92.62%
CHEMBL4208 P20618 Proteasome component C5 81.01% 90.00%
CHEMBL5747 Q92793 CREB-binding protein 80.20% 95.12%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.09% 90.71%

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.
Hernandia nymphaeifolia
Lindera chunii

Cross-Links

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PubChem 500429
LOTUS LTS0074373
wikiData Q27135475