L-Dopachrome

Details

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Internal ID 5369a467-d92f-4fc4-a3ba-57206fdfcf7a
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > L-alpha-amino acids
IUPAC Name (2S)-5,6-dioxo-2,3-dihydro-1H-indole-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H7NO4/c11-7-2-4-1-6(9(13)14)10-5(4)3-8(7)12/h2-3,6,10H,1H2,(H,13,14)/t6-/m0/s1
InChI Key VJNCICVKUHKIIV-LURJTMIESA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C9H7NO4
Molecular Weight 193.16 g/mol
Exact Mass 193.03750770 g/mol
Topological Polar Surface Area (TPSA) 83.50 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.61
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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2-L-carboxy-2,3-dihydroindole-5,6-quinone
CHEBI:15772
DTXSID501046666
(2S)-5,6-dioxo-2,3-dihydro-1H-indole-2-carboxylate
RefChem:1088162
(2S)-5,6-dioxo-2,3-dihydro-1H-indole-2-carboxylic acid
DTXCID301528488
Dopachrome, (S)-
89762-39-0
63LR8AMX5R
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of L-Dopachrome

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9903 99.03%
Caco-2 - 0.8535 85.35%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6243 62.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9453 94.53%
OATP1B3 inhibitior + 0.9459 94.59%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9392 93.92%
P-glycoprotein inhibitior - 0.9905 99.05%
P-glycoprotein substrate - 0.8502 85.02%
CYP3A4 substrate - 0.6186 61.86%
CYP2C9 substrate - 0.7983 79.83%
CYP2D6 substrate - 0.8514 85.14%
CYP3A4 inhibition - 0.9897 98.97%
CYP2C9 inhibition - 0.8639 86.39%
CYP2C19 inhibition - 0.8714 87.14%
CYP2D6 inhibition - 0.8843 88.43%
CYP1A2 inhibition - 0.7437 74.37%
CYP2C8 inhibition - 0.9850 98.50%
CYP inhibitory promiscuity - 0.9387 93.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5932 59.32%
Eye corrosion - 0.9800 98.00%
Eye irritation + 0.9617 96.17%
Skin irritation - 0.7220 72.20%
Skin corrosion - 0.9265 92.65%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8177 81.77%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.7283 72.83%
skin sensitisation - 0.8103 81.03%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.5905 59.05%
Acute Oral Toxicity (c) III 0.4690 46.90%
Estrogen receptor binding - 0.9426 94.26%
Androgen receptor binding - 0.7235 72.35%
Thyroid receptor binding - 0.7415 74.15%
Glucocorticoid receptor binding - 0.8981 89.81%
Aromatase binding - 0.7466 74.66%
PPAR gamma - 0.7363 73.63%
Honey bee toxicity - 0.8582 85.82%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.4102 41.02%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.77% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.07% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.51% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.02% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.13% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.41% 94.45%

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 5459802
LOTUS LTS0036169
wikiData Q27098224