Nhatrangin A

Details

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Internal ID 25555c99-38cb-4576-be5f-c769e511e4e5
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzylethers
IUPAC Name (2R,3R,4S,7S)-3-[(3R,4R)-3,4-dihydroxypentanoyl]oxy-7-(3-hydroxyphenyl)-7-methoxy-2,4-dimethylheptanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H32O8/c1-12(8-9-18(28-4)15-6-5-7-16(23)10-15)20(13(2)21(26)27)29-19(25)11-17(24)14(3)22/h5-7,10,12-14,17-18,20,22-24H,8-9,11H2,1-4H3,(H,26,27)/t12-,13+,14+,17+,18-,20+/m0/s1
InChI Key SDQFZZGLPYJDFO-IKZAZAHWSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O8
Molecular Weight 412.50 g/mol
Exact Mass 412.20971797 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 12

Synonyms

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DTXSID301334134

2D Structure

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2D Structure of Nhatrangin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9552 95.52%
Caco-2 - 0.6871 68.71%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7824 78.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8742 87.42%
OATP1B3 inhibitior + 0.8745 87.45%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7303 73.03%
P-glycoprotein inhibitior - 0.6261 62.61%
P-glycoprotein substrate - 0.5255 52.55%
CYP3A4 substrate + 0.5592 55.92%
CYP2C9 substrate - 0.5872 58.72%
CYP2D6 substrate - 0.8445 84.45%
CYP3A4 inhibition - 0.8705 87.05%
CYP2C9 inhibition - 0.9300 93.00%
CYP2C19 inhibition - 0.9132 91.32%
CYP2D6 inhibition - 0.9349 93.49%
CYP1A2 inhibition - 0.7868 78.68%
CYP2C8 inhibition - 0.7440 74.40%
CYP inhibitory promiscuity - 0.9897 98.97%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.7115 71.15%
Eye corrosion - 0.9814 98.14%
Eye irritation - 0.9743 97.43%
Skin irritation - 0.7803 78.03%
Skin corrosion - 0.9197 91.97%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3809 38.09%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5599 55.99%
skin sensitisation - 0.8590 85.90%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.6197 61.97%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.5524 55.24%
Acute Oral Toxicity (c) III 0.7584 75.84%
Estrogen receptor binding + 0.7472 74.72%
Androgen receptor binding - 0.5216 52.16%
Thyroid receptor binding + 0.5471 54.71%
Glucocorticoid receptor binding + 0.6061 60.61%
Aromatase binding - 0.5911 59.11%
PPAR gamma + 0.5230 52.30%
Honey bee toxicity - 0.7547 75.47%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.8777 87.77%

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
CHEMBL2581 P07339 Cathepsin D 98.74% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.59% 96.09%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 93.25% 94.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.13% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.86% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.27% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.07% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.79% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.61% 96.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.55% 93.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.06% 95.50%
CHEMBL2535 P11166 Glucose transporter 88.68% 98.75%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.71% 94.62%
CHEMBL340 P08684 Cytochrome P450 3A4 87.03% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 85.81% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.75% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.63% 85.14%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.38% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 46211050
LOTUS LTS0131245
wikiData Q105250778