Novae-zelandin B

Details

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Internal ID 0a2dd0c8-7076-43a1-97d8-5ce7d687ad58
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name (E)-4-(4-methoxy-2-methyl-6-oxopyran-3-yl)but-2-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O5/c1-7-8(4-3-5-10(12)13)9(15-2)6-11(14)16-7/h3,5-6H,4H2,1-2H3,(H,12,13)/b5-3+
InChI Key OUSIFRGZULVWQP-HWKANZROSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O5
Molecular Weight 224.21 g/mol
Exact Mass 224.06847348 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.14
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Novae-zelandin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9153 91.53%
Caco-2 + 0.6103 61.03%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8061 80.61%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.8795 87.95%
OATP1B3 inhibitior + 0.9598 95.98%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7990 79.90%
P-glycoprotein inhibitior - 0.9687 96.87%
P-glycoprotein substrate - 0.9429 94.29%
CYP3A4 substrate - 0.5922 59.22%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate - 0.8877 88.77%
CYP3A4 inhibition - 0.8207 82.07%
CYP2C9 inhibition - 0.7372 73.72%
CYP2C19 inhibition - 0.5797 57.97%
CYP2D6 inhibition - 0.8660 86.60%
CYP1A2 inhibition - 0.8281 82.81%
CYP2C8 inhibition - 0.7056 70.56%
CYP inhibitory promiscuity - 0.6522 65.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8467 84.67%
Carcinogenicity (trinary) Non-required 0.7106 71.06%
Eye corrosion - 0.9461 94.61%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.6508 65.08%
Skin corrosion - 0.9376 93.76%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5290 52.90%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8472 84.72%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.8044 80.44%
Acute Oral Toxicity (c) II 0.4558 45.58%
Estrogen receptor binding - 0.8157 81.57%
Androgen receptor binding + 0.5770 57.70%
Thyroid receptor binding - 0.8866 88.66%
Glucocorticoid receptor binding - 0.6617 66.17%
Aromatase binding - 0.6417 64.17%
PPAR gamma - 0.5245 52.45%
Honey bee toxicity - 0.9469 94.69%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7034 70.34%
Fish aquatic toxicity + 0.9607 96.07%

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 94.22% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.21% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 94.03% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.27% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.05% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.47% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.03% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 85.65% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.08% 97.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.79% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.70% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.93% 95.50%
CHEMBL4208 P20618 Proteasome component C5 80.87% 90.00%

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.
There are no matching plants.

Cross-Links

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PubChem 101379191
LOTUS LTS0234682
wikiData Q77424167