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4-methoxy-1-naphthoic+acid
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4-methoxy-1-naphthoic+acid
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041958-1G , MDL Number: MFCD01863049
Supplier:
Bachem Americas
Description:
Sequence: Fmoc-His(1-Me)-OH
Supplier:
Thermo Scientific Chemicals
Description:
a-Fmoc-1-trityl-D-histidine, 98%
Supplier:
BeanTown Chemical
Description:
CAS: 26218-80-4; MDL No: MFCD00674130
Solid; Molecular Formula: C8H9NO3; MW: 167.16
Melting Point: 48-53°
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041611-1G , MDL Number: MFCD02094127
Supplier:
Bachem Americas
Description:
Sequence: Fmoc-p-amino-Phe(Boc)-OH
Supplier:
MilliporeSigma
Description:
Functions as a coenzyme of a large number of oxidoreductases.
Supplier:
ALADDIN SCIENTIFIC
Description:
It is a 3-substituted isoxazole derivative. It is a structural isomer of 5-aminoisoxazole.It may be used in the following studies: . As a reagent in the synthesis of N-(4-(N-isoxazol-3-ylsulfamoyl)phenyl)acetamide. . As a starting material in the synthesis of N-(isoxazol-3-yl)-N’-(carbomethoxy)thiourea. . As a starting material in the synthesis of (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxy-iminoacetic acid, a side-chain of the fourth generation of cephem antibiotics.
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041944-1G , MDL Number: MFCD01311771
Supplier:
Enzo Life Sciences
Description:
Microcystins are a group of cyclic heptapeptide hepatotoxins produced by a number of cyanobacterial genera. The most notable of which, and namesake, is the widespread genus Microcystis. Structurally, all microcystins consist of the generalized structure cyclo(-D-Ala1-X2-D-MeAsp3-Y4-Adda5-D-Glu6-Mdha7-). X and Y are variable L-amino acids, D-MeAsp is D-erythro-β-methylaspartic acid and Mdha is N-methyldehydroalanine. Adda is the cyanobacteria unique C20 β-amino acid 3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-deca-4,6-dienoic acid. Substitutions of the variable L-amino acids at positions 2 and 4 give rise to at least 21 known primary microcystin analogs and alterations in the other constituent amino acids result in more than 90 reported mycrocystins to date.
Supplier:
Enzo Life Sciences
Description:
Microcystins are a group of cyclic heptapeptide hepatotoxins produced by a number of cyanobacterial genera. The most notable of which, and namesake, is the widespread genus Microcystis. Structurally, all microcystins consist of the generalized structure cyclo(-D-Ala1-X2-D-MeAsp3-Y4-Adda5-D-Glu6-Mdha7-). X and Y are variable L-amino acids, D-MeAsp is D-erythro-ß-methylaspartic acid and Mdha is N-methyldehydroalanine. Adda is the cyanobacteria unique C20 ß-amino acid 3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-deca-4,6-dienoic acid. Substitutions of the variable L-amino acids at positions 2 and 4 give rise to at least 21 known primary microcystin analogs and alterations in the other constituent amino acids result in more than 90 reported mycrocystins to date.
Supplier:
TCI America
Description:
CAS Number: 7338-27-4
MDL Number: MFCD00021713 Molecular Formula: C6H8O4 Molecular Weight: 144.13 Purity/Analysis Method: >98.0% (GC,T) Form: Crystal Boiling point (°C): 149 Melting point (°C): 72
Supplier:
Thermo Scientific Chemicals
Description:
5g CAS: 201484-50-6, MDL: MFCD00672337
Supplier:
Bachem Americas
Description:
Sequence: Fmoc-Phg-OH
Supplier:
Thermo Scientific Chemicals
Description:
A broad spectrum antibiotic commonly used against bacteria which cause sinus and lung infections
Catalog Number:
(B-3795.0001BA)
Supplier:
Bachem Americas
Description:
Besides a large selection of tyrosine derivatives, Bachem offers derivatives of O-alkylated tyrosines, thyronine, phosphotyrosine and sulfotyrosine. Bachem additionally offers H-[¹⁵N]Tyr-OH, E-3245.
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