7-(3-methylbut-2-enyl)-L-tryptophan

Details

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Internal ID 7e175a3e-3f17-46b2-a7d1-b0b775f96c19
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolyl carboxylic acids and derivatives
IUPAC Name (2S)-2-amino-3-[7-(3-methylbut-2-enyl)-1H-indol-3-yl]propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H20N2O2/c1-10(2)6-7-11-4-3-5-13-12(9-18-15(11)13)8-14(17)16(19)20/h3-6,9,14,18H,7-8,17H2,1-2H3,(H,19,20)/t14-/m0/s1
InChI Key OLFAGKNOXHVNHG-AWEZNQCLSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20N2O2
Molecular Weight 272.34 g/mol
Exact Mass 272.152477885 g/mol
Topological Polar Surface Area (TPSA) 79.10 Ų
XlogP 0.90
Atomic LogP (AlogP) 2.63
H-Bond Acceptor 2
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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7-(3-methylbut-2-en-1-yl)-L-tryptophan
7-dimethylallyltryptophan
CHEBI:59356
C19767
Q27126649

2D Structure

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2D Structure of 7-(3-methylbut-2-enyl)-L-tryptophan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5795 57.95%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.3842 38.42%
OATP2B1 inhibitior - 0.7174 71.74%
OATP1B1 inhibitior + 0.9420 94.20%
OATP1B3 inhibitior + 0.9420 94.20%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8398 83.98%
P-glycoprotein inhibitior - 0.9261 92.61%
P-glycoprotein substrate - 0.7276 72.76%
CYP3A4 substrate - 0.5300 53.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7513 75.13%
CYP3A4 inhibition - 0.9129 91.29%
CYP2C9 inhibition - 0.7918 79.18%
CYP2C19 inhibition - 0.8335 83.35%
CYP2D6 inhibition - 0.8668 86.68%
CYP1A2 inhibition - 0.7554 75.54%
CYP2C8 inhibition - 0.7928 79.28%
CYP inhibitory promiscuity - 0.7883 78.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.6729 67.29%
Eye corrosion - 0.9927 99.27%
Eye irritation - 0.9774 97.74%
Skin irritation - 0.8039 80.39%
Skin corrosion - 0.9233 92.33%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.6974 69.74%
Hepatotoxicity + 0.5492 54.92%
skin sensitisation - 0.8265 82.65%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.8653 86.53%
Acute Oral Toxicity (c) III 0.4574 45.74%
Estrogen receptor binding + 0.6945 69.45%
Androgen receptor binding - 0.6815 68.15%
Thyroid receptor binding + 0.5759 57.59%
Glucocorticoid receptor binding + 0.6379 63.79%
Aromatase binding + 0.6384 63.84%
PPAR gamma + 0.8470 84.70%
Honey bee toxicity - 0.9263 92.63%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.8673 86.73%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.99% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 96.59% 83.82%
CHEMBL2581 P07339 Cathepsin D 95.10% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.56% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.14% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 91.82% 94.73%
CHEMBL1255126 O15151 Protein Mdm4 90.80% 90.20%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.03% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.79% 86.33%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 87.86% 83.10%
CHEMBL221 P23219 Cyclooxygenase-1 86.72% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.40% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.67% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.36% 96.00%
CHEMBL2535 P11166 Glucose transporter 82.00% 98.75%
CHEMBL213 P08588 Beta-1 adrenergic receptor 81.88% 95.56%
CHEMBL284 P27487 Dipeptidyl peptidase IV 81.85% 95.69%

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 45479458
LOTUS LTS0267091
wikiData Q27126649