Hernovine

Details

Top
Internal ID 970b92ba-0d27-4aea-b367-c76da9c76831
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name (6aS)-1,11-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,10-diol
SMILES (Canonical) COC1=C(C=CC2=C1C3=C4C(C2)NCCC4=CC(=C3OC)O)O
SMILES (Isomeric) COC1=C(C=CC2=C1C3=C4[C@H](C2)NCCC4=CC(=C3OC)O)O
InChI InChI=1S/C18H19NO4/c1-22-17-12(20)4-3-9-7-11-14-10(5-6-19-11)8-13(21)18(23-2)16(14)15(9)17/h3-4,8,11,19-21H,5-7H2,1-2H3/t11-/m0/s1
InChI Key YHVSWHLQYUURMP-NSHDSACASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C18H19NO4
Molecular Weight 313.30 g/mol
Exact Mass 313.13140809 g/mol
Topological Polar Surface Area (TPSA) 71.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
L-(+)-Hernovine
CHEMBL512052
5544-69-4

2D Structure

Top
2D Structure of Hernovine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9664 96.64%
Caco-2 + 0.6893 68.93%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6245 62.45%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.9321 93.21%
OATP1B3 inhibitior + 0.9574 95.74%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.5448 54.48%
P-glycoprotein inhibitior - 0.8355 83.55%
P-glycoprotein substrate - 0.7861 78.61%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6360 63.60%
CYP2D6 substrate + 0.7728 77.28%
CYP3A4 inhibition - 0.8529 85.29%
CYP2C9 inhibition - 0.9327 93.27%
CYP2C19 inhibition - 0.8031 80.31%
CYP2D6 inhibition + 0.5852 58.52%
CYP1A2 inhibition - 0.5238 52.38%
CYP2C8 inhibition - 0.6242 62.42%
CYP inhibitory promiscuity - 0.8538 85.38%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7423 74.23%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8565 85.65%
Skin irritation - 0.6813 68.13%
Skin corrosion - 0.9192 91.92%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7496 74.96%
Micronuclear - 0.5100 51.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8787 87.87%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.8801 88.01%
Acute Oral Toxicity (c) III 0.5164 51.64%
Estrogen receptor binding + 0.6774 67.74%
Androgen receptor binding + 0.6642 66.42%
Thyroid receptor binding + 0.7336 73.36%
Glucocorticoid receptor binding + 0.7732 77.32%
Aromatase binding - 0.5378 53.78%
PPAR gamma + 0.7769 77.69%
Honey bee toxicity - 0.9201 92.01%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity - 0.5662 56.62%

Targets

Top

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 99.07% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.81% 93.99%
CHEMBL1951 P21397 Monoamine oxidase A 97.30% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.23% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.24% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.78% 97.09%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 90.17% 92.68%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 90.17% 91.79%
CHEMBL217 P14416 Dopamine D2 receptor 88.27% 95.62%
CHEMBL4208 P20618 Proteasome component C5 87.61% 90.00%
CHEMBL3438 Q05513 Protein kinase C zeta 85.44% 88.48%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.24% 95.89%
CHEMBL213 P08588 Beta-1 adrenergic receptor 85.19% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.73% 86.33%
CHEMBL2581 P07339 Cathepsin D 84.06% 98.95%
CHEMBL2535 P11166 Glucose transporter 83.55% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.33% 99.17%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.34% 92.94%
CHEMBL2056 P21728 Dopamine D1 receptor 80.77% 91.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.33% 91.03%

Plants that contains it

Top
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.
Avena fatua
Helichrysum fulvum
Hernandia sonora
Illigera luzonensis
Piper sylvaticum

Cross-Links

Top
PubChem 10425723
NPASS NPC66341
LOTUS LTS0185413
wikiData Q105348635