N-Methyl hernangerin

Details

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Internal ID 813cb3a9-8861-4755-afe7-64eb9fcf541a
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name (12S)-18-methoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-17-ol
SMILES (Canonical) CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)O)OC)OCO3
SMILES (Isomeric) CN1CCC2=CC3=C(C4=C2[C@@H]1CC5=C4C(=C(C=C5)O)OC)OCO3
InChI InChI=1S/C19H19NO4/c1-20-6-5-11-8-14-19(24-9-23-14)17-15(11)12(20)7-10-3-4-13(21)18(22-2)16(10)17/h3-4,8,12,21H,5-7,9H2,1-2H3/t12-/m0/s1
InChI Key WOIZHRXESCUSGM-LBPRGKRZSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H19NO4
Molecular Weight 325.40 g/mol
Exact Mass 325.13140809 g/mol
Topological Polar Surface Area (TPSA) 51.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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NSC785147
NSC785181
NSC785182
NSC-785147
NSC-785181
NSC-785182
(12S)-18-Methoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-17-ol
5H-1,3-Benzodioxolo[6,5,4-de]benzo[g]quinolin-11-ol, 6,7,7a,8-tetrahydro-12-methoxy-7-methyl-, (7aS)-

2D Structure

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2D Structure of N-Methyl hernangerin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9327 93.27%
Caco-2 + 0.8928 89.28%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Lysosomes 0.4444 44.44%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9433 94.33%
OATP1B3 inhibitior + 0.9500 95.00%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.6015 60.15%
P-glycoprotein inhibitior - 0.8717 87.17%
P-glycoprotein substrate - 0.7976 79.76%
CYP3A4 substrate + 0.5907 59.07%
CYP2C9 substrate - 0.6106 61.06%
CYP2D6 substrate + 0.6924 69.24%
CYP3A4 inhibition + 0.5887 58.87%
CYP2C9 inhibition - 0.8908 89.08%
CYP2C19 inhibition + 0.6242 62.42%
CYP2D6 inhibition + 0.8177 81.77%
CYP1A2 inhibition + 0.5485 54.85%
CYP2C8 inhibition - 0.8368 83.68%
CYP inhibitory promiscuity - 0.6472 64.72%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6205 62.05%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9418 94.18%
Skin irritation - 0.7863 78.63%
Skin corrosion - 0.9464 94.64%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7383 73.83%
Micronuclear + 0.5200 52.00%
Hepatotoxicity - 0.8375 83.75%
skin sensitisation - 0.8639 86.39%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.8968 89.68%
Acute Oral Toxicity (c) III 0.7478 74.78%
Estrogen receptor binding + 0.7731 77.31%
Androgen receptor binding - 0.4866 48.66%
Thyroid receptor binding - 0.5338 53.38%
Glucocorticoid receptor binding + 0.7974 79.74%
Aromatase binding - 0.4941 49.41%
PPAR gamma + 0.7751 77.51%
Honey bee toxicity - 0.8834 88.34%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9183 91.83%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.55% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.41% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.95% 96.77%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 95.33% 93.40%
CHEMBL1951 P21397 Monoamine oxidase A 94.54% 91.49%
CHEMBL217 P14416 Dopamine D2 receptor 92.56% 95.62%
CHEMBL261 P00915 Carbonic anhydrase I 92.51% 96.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.45% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.65% 94.45%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 90.87% 91.79%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.70% 93.99%
CHEMBL2056 P21728 Dopamine D1 receptor 90.42% 91.00%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 89.25% 82.67%
CHEMBL4208 P20618 Proteasome component C5 89.23% 90.00%
CHEMBL2581 P07339 Cathepsin D 88.70% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.56% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.56% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.26% 86.33%
CHEMBL3438 Q05513 Protein kinase C zeta 86.10% 88.48%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 84.75% 82.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.43% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.58% 94.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.89% 91.03%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.22% 95.78%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.90% 89.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.15% 89.00%

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.
Ficus carica
Hernandia sonora
Lindera chunii

Cross-Links

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PubChem 497829
NPASS NPC308691
LOTUS LTS0161933
wikiData Q105309529