Kopsihainanine B

Details

Top
Internal ID b7f41d7e-3559-446d-bc69-50804323ffd4
Taxonomy Alkaloids and derivatives > Aspidofractine alkaloids
IUPAC Name (1R,4S,12R,13S,16R)-17-oxo-5,14-diazahexacyclo[12.4.3.01,13.04,12.06,11.012,16]henicosa-6,8,10-triene-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H22N2O3/c23-15-10-18-6-3-9-22-11-13(15)20(16(18)22)12-4-1-2-5-14(12)21-19(20,8-7-18)17(24)25/h1-2,4-5,13,16,21H,3,6-11H2,(H,24,25)/t13-,16+,18-,19-,20+/m1/s1
InChI Key VMYIEWNUGAYDHM-MKCULMFZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C20H22N2O3
Molecular Weight 338.40 g/mol
Exact Mass 338.16304257 g/mol
Topological Polar Surface Area (TPSA) 69.60 Ų
XlogP -0.60
Atomic LogP (AlogP) 2.02
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Kopsihainanine B

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8402 84.02%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7401 74.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9267 92.67%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8414 84.14%
P-glycoprotein inhibitior - 0.9455 94.55%
P-glycoprotein substrate - 0.6231 62.31%
CYP3A4 substrate + 0.5860 58.60%
CYP2C9 substrate - 0.7999 79.99%
CYP2D6 substrate + 0.3647 36.47%
CYP3A4 inhibition - 0.7927 79.27%
CYP2C9 inhibition - 0.8776 87.76%
CYP2C19 inhibition - 0.8400 84.00%
CYP2D6 inhibition - 0.8050 80.50%
CYP1A2 inhibition - 0.7102 71.02%
CYP2C8 inhibition - 0.9015 90.15%
CYP inhibitory promiscuity - 0.9770 97.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6368 63.68%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9889 98.89%
Skin irritation - 0.7762 77.62%
Skin corrosion - 0.9352 93.52%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4753 47.53%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.6015 60.15%
skin sensitisation - 0.8383 83.83%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.7296 72.96%
Acute Oral Toxicity (c) III 0.5521 55.21%
Estrogen receptor binding - 0.6182 61.82%
Androgen receptor binding + 0.7509 75.09%
Thyroid receptor binding - 0.5941 59.41%
Glucocorticoid receptor binding - 0.4694 46.94%
Aromatase binding + 0.5897 58.97%
PPAR gamma + 0.6336 63.36%
Honey bee toxicity - 0.9302 93.02%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.3734 37.34%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.80% 95.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 93.06% 93.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.92% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.67% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.58% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.64% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.94% 82.69%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.55% 93.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.36% 96.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.29% 93.04%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.28% 94.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.38% 97.09%
CHEMBL4208 P20618 Proteasome component C5 84.23% 90.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 83.82% 94.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.62% 97.25%
CHEMBL5028 O14672 ADAM10 82.57% 97.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.25% 86.33%
CHEMBL3524 P56524 Histone deacetylase 4 81.14% 92.97%

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.
Kopsia hainanensis

Cross-Links

Top
PubChem 54590592
LOTUS LTS0270842
wikiData Q105289395