An esterified form of L-ANAP
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L-ANAP methyl ester (hydrochloride)

Item No. 15437

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
3-[(6-acetyl-2-naphthalenyl)amino]-L-alanine, methyl ester, monohydrochloride
Molecular Formula
C16H18N2O3 • HCl
Formula Weight
322.8
Purity
≥95%
Formulation (Request formulation change)
A solid
Solubility(Learn about Variance in Solubility)
DMF: 10 mg/mlDMSO: 10 mg/mlEthanol: 0.5 mg/ml
λmax
248, 256, 354 nm
SMILES
CC(C1=CC2=CC=C(NC[C@H](N)C(OC)=O)C=C2C=C1)=O.Cl
InChi Code
InChI=1S/C16H18N2O3.ClH/c1-10(19)11-3-4-13-8-14(6-5-12(13)7-11)18-9-15(17)16(20)21-2;/h3-8,15,18H,9,17H2,1-2H3;1H/t15-;/m0./s1
InChi Key
BDDDZPULRTXFQM-RSAXXLAASA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    500 µg

    $90

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    1 mg

    $152

    Add

    5 mg

    $624

    Add
    Product Description

    L-ANAP methyl ester is an esterified form of the fluorescent unnatural amino acid L-ANAP (Item No. 15436).1 It has been used in the synthesis of L-ANAP. L-ANAP methyl ester has also been used to fluorescently label proteins in vitro through genetic encoding.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Xiang, Z., and Wang, L. Enantiospecific synthesis of genetically encodable fluorescent unnatural amino acid L-3-(6-acetylnaphthalen-2-ylamino)-2-aminopropanoic acid. The Journal of Organic Chemistry 76(15), 6367-6371 (2011).

    2. Berlin, J.R., Lopez, W., Jain, M.R., et al. Use of the methyl ester of a fluorescent unnatural amino acid to facilitate site-specific incorporation of fluorescent probes in proteins. Biophys. J. 108(2), 624A-625A (2015).