(3s)2,3-Dihydro-l-tryptophan

Details

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Internal ID 02bebc6d-9ca9-4d5d-b95a-a010092b858f
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolyl carboxylic acids and derivatives
IUPAC Name (2S)-2-amino-3-[(3S)-2,3-dihydro-1H-indol-3-yl]propanoic acid
SMILES (Canonical) C1C(C2=CC=CC=C2N1)CC(C(=O)O)N
SMILES (Isomeric) C1[C@H](C2=CC=CC=C2N1)C[C@@H](C(=O)O)N
InChI InChI=1S/C11H14N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,7,9,13H,5-6,12H2,(H,14,15)/t7-,9+/m1/s1
InChI Key SPHNJDOWMOXSMT-APPZFPTMSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H14N2O2
Molecular Weight 206.24 g/mol
Exact Mass 206.105527694 g/mol
Topological Polar Surface Area (TPSA) 75.40 Ų
XlogP -1.50
Atomic LogP (AlogP) 1.00
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3s)2,3-Dihydro-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 + 0.9957 99.57%
Caco-2 - 0.6605 66.05%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.4271 42.71%
OATP2B1 inhibitior - 0.8656 86.56%
OATP1B1 inhibitior + 0.9597 95.97%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8812 88.12%
P-glycoprotein inhibitior - 0.9904 99.04%
P-glycoprotein substrate - 0.8642 86.42%
CYP3A4 substrate - 0.6060 60.60%
CYP2C9 substrate - 0.6027 60.27%
CYP2D6 substrate - 0.6884 68.84%
CYP3A4 inhibition - 0.9799 97.99%
CYP2C9 inhibition - 0.9674 96.74%
CYP2C19 inhibition - 0.9592 95.92%
CYP2D6 inhibition - 0.9402 94.02%
CYP1A2 inhibition - 0.5575 55.75%
CYP2C8 inhibition - 0.7528 75.28%
CYP inhibitory promiscuity - 0.9794 97.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.7413 74.13%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9909 99.09%
Skin irritation - 0.8098 80.98%
Skin corrosion - 0.9348 93.48%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7686 76.86%
Micronuclear + 0.6874 68.74%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.8648 86.48%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.8687 86.87%
Acute Oral Toxicity (c) III 0.4512 45.12%
Estrogen receptor binding - 0.7842 78.42%
Androgen receptor binding - 0.6679 66.79%
Thyroid receptor binding - 0.7511 75.11%
Glucocorticoid receptor binding - 0.6408 64.08%
Aromatase binding - 0.7321 73.21%
PPAR gamma - 0.5934 59.34%
Honey bee toxicity - 0.9653 96.53%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.7675 76.75%

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 98.61% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.84% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.75% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.70% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.87% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.55% 95.56%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 84.87% 94.08%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.85% 94.62%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.72% 93.56%

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.
Ageratum conyzoides
Atractylodes lancea
Bupleurum chinense
Codonopsis pilosula
Fagopyrum esculentum
Isatis tinctoria
Juncus effusus
Lycium chinense
Piper kadsura
Reynoutria japonica

Cross-Links

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PubChem 56844224
NPASS NPC209054