Nevaltophin E

Details

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Internal ID 602031cd-d481-4126-922c-e6bad5d113dc
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name (2S)-N-[2-(1H-indol-3-yl)ethyl]-3-methyl-2-[methyl-(3-methyl-2-oxobutanoyl)amino]butanamide
SMILES (Canonical) CC(C)C(C(=O)NCCC1=CNC2=CC=CC=C21)N(C)C(=O)C(=O)C(C)C
SMILES (Isomeric) CC(C)[C@@H](C(=O)NCCC1=CNC2=CC=CC=C21)N(C)C(=O)C(=O)C(C)C
InChI InChI=1S/C21H29N3O3/c1-13(2)18(24(5)21(27)19(25)14(3)4)20(26)22-11-10-15-12-23-17-9-7-6-8-16(15)17/h6-9,12-14,18,23H,10-11H2,1-5H3,(H,22,26)/t18-/m0/s1
InChI Key FGEYVSARJMKCGF-SFHVURJKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H29N3O3
Molecular Weight 371.50 g/mol
Exact Mass 371.22089180 g/mol
Topological Polar Surface Area (TPSA) 82.30 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Nevaltophin E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9577 95.77%
Caco-2 + 0.5560 55.60%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6397 63.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9209 92.09%
OATP1B3 inhibitior + 0.9446 94.46%
MATE1 inhibitior - 0.7644 76.44%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6767 67.67%
P-glycoprotein inhibitior + 0.6124 61.24%
P-glycoprotein substrate + 0.7459 74.59%
CYP3A4 substrate + 0.6037 60.37%
CYP2C9 substrate - 0.6012 60.12%
CYP2D6 substrate - 0.8192 81.92%
CYP3A4 inhibition - 0.7085 70.85%
CYP2C9 inhibition - 0.7971 79.71%
CYP2C19 inhibition + 0.5340 53.40%
CYP2D6 inhibition - 0.8997 89.97%
CYP1A2 inhibition + 0.5447 54.47%
CYP2C8 inhibition - 0.8627 86.27%
CYP inhibitory promiscuity + 0.6387 63.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6866 68.66%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9927 99.27%
Skin irritation - 0.8006 80.06%
Skin corrosion - 0.9302 93.02%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8752 87.52%
Micronuclear + 0.6800 68.00%
Hepatotoxicity - 0.7757 77.57%
skin sensitisation - 0.9029 90.29%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.9160 91.60%
Acute Oral Toxicity (c) III 0.6474 64.74%
Estrogen receptor binding + 0.6246 62.46%
Androgen receptor binding - 0.6193 61.93%
Thyroid receptor binding + 0.6761 67.61%
Glucocorticoid receptor binding + 0.6169 61.69%
Aromatase binding - 0.4920 49.20%
PPAR gamma - 0.5563 55.63%
Honey bee toxicity - 0.8971 89.71%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.8896 88.96%

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 99.04% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.51% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.41% 96.09%
CHEMBL1914 P06276 Butyrylcholinesterase 97.30% 95.00%
CHEMBL3310 Q96DB2 Histone deacetylase 11 91.53% 88.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.51% 95.56%
CHEMBL2885 P07451 Carbonic anhydrase III 90.09% 87.45%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 87.89% 90.71%
CHEMBL255 P29275 Adenosine A2b receptor 87.81% 98.59%
CHEMBL221 P23219 Cyclooxygenase-1 87.40% 90.17%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 86.45% 89.33%
CHEMBL5103 Q969S8 Histone deacetylase 10 86.44% 90.08%
CHEMBL5028 O14672 ADAM10 85.83% 97.50%
CHEMBL3401 O75469 Pregnane X receptor 82.66% 94.73%
CHEMBL4208 P20618 Proteasome component C5 81.14% 90.00%
CHEMBL4073 P09237 Matrix metalloproteinase 7 81.13% 97.56%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 80.87% 95.48%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.83% 89.00%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 80.35% 83.10%
CHEMBL2996 Q05655 Protein kinase C delta 80.32% 97.79%

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 132509312
LOTUS LTS0034399
wikiData Q104994863