3-Methyl-L-Histidine

Details

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Internal ID 8c7e0b28-736a-43d4-9192-37d0d237fc3e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Histidine and derivatives
IUPAC Name (2S)-2-amino-3-(3-methylimidazol-4-yl)propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H11N3O2/c1-10-4-9-3-5(10)2-6(8)7(11)12/h3-4,6H,2,8H2,1H3,(H,11,12)/t6-/m0/s1
InChI Key JDHILDINMRGULE-LURJTMIESA-N
Popularity 1,855 references in papers

Physical and Chemical Properties

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Molecular Formula C7H11N3O2
Molecular Weight 169.18 g/mol
Exact Mass 169.085126602 g/mol
Topological Polar Surface Area (TPSA) 81.10 Ų
XlogP -3.30
Atomic LogP (AlogP) -0.63
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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368-16-1
3-Methylhistidine
H-His(3-Me)-OH
(S)-2-Amino-3-(1-methyl-1H-imidazol-5-yl)propanoic acid
L-Histidine, 3-methyl-
3-N-Methyl-L-histidine
N(pi)-Methyl-L-histidine
N(pros)-methyl-L-histidine
Tau-methylhistidine
L-3-Methylhistidine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Methyl-L-Histidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9798 97.98%
Caco-2 + 0.4912 49.12%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.5009 50.09%
OATP2B1 inhibitior - 0.8627 86.27%
OATP1B1 inhibitior + 0.9451 94.51%
OATP1B3 inhibitior + 0.9455 94.55%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8482 84.82%
P-glycoprotein inhibitior - 0.9901 99.01%
P-glycoprotein substrate - 0.9108 91.08%
CYP3A4 substrate - 0.7679 76.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8415 84.15%
CYP3A4 inhibition - 0.7545 75.45%
CYP2C9 inhibition - 0.9554 95.54%
CYP2C19 inhibition - 0.9497 94.97%
CYP2D6 inhibition - 0.9405 94.05%
CYP1A2 inhibition - 0.9277 92.77%
CYP2C8 inhibition - 0.9608 96.08%
CYP inhibitory promiscuity - 0.9773 97.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6126 61.26%
Eye corrosion - 0.9788 97.88%
Eye irritation - 0.9407 94.07%
Skin irritation - 0.7022 70.22%
Skin corrosion - 0.8901 89.01%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8012 80.12%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.6343 63.43%
skin sensitisation - 0.9028 90.28%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.9163 91.63%
Acute Oral Toxicity (c) III 0.5083 50.83%
Estrogen receptor binding - 0.9140 91.40%
Androgen receptor binding - 0.8514 85.14%
Thyroid receptor binding - 0.8521 85.21%
Glucocorticoid receptor binding - 0.7369 73.69%
Aromatase binding - 0.8769 87.69%
PPAR gamma - 0.8370 83.70%
Honey bee toxicity - 0.9877 98.77%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.8097 80.97%

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 99.08% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 98.49% 83.82%
CHEMBL2581 P07339 Cathepsin D 91.61% 98.95%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 89.22% 92.29%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.96% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 86.33% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.77% 95.56%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.91% 90.24%

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 64969
LOTUS LTS0239491
wikiData Q18416004