4281 Results for: "cis-1,3-Dibenzyl-2-oxo-4,5-imidazolidinecarboxylic acid"

Supplier: TCI America

CAS Number: 84-57-1
MDL Number: MFCD00035706
Molecular Formula: C10H8Cl2N2O4S
Molecular Weight: 323.14
Purity/Analysis Method: >98.0% (T)
Form: Crystal

Supplier: TCI America

CAS Number: 1492-18-8 MDL Number: MFCD00006704 Molecular Formula: C20H23N7O7 Molecular Weight: 511.51 Purity/Analysis Method: 98.0% (HPLC,T) Form: Crystal

Supplier: Spectrum Chemicals

FD and C Blue No. 1 | Non-graded FD and C Blue No. 1 supplied by Spectrum is indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.

Supplier: TCI America

CAS Number: 37910-77-3
MDL Number: MFCD00027405
Molecular Formula: C24H46O2
Molecular Weight: 366.63
Purity/Analysis Method: >95.0% (GC)
Form: Clear Liquid
Boiling point (°C): 233
Specific Gravity (20/20): 0.87

Supplier: Enzo Life Sciences

Fluoroquinolone with broad spectrum antibacterial activity against Gram-positive and Gram-negative bacteria.

Supplier: Bachem Americas

Sequence: Boc-cis-4-fluoro-Pro-OH

Supplier: TCI America

CAS Number: 203866-13-1
MDL Number: MFCD04973957
Molecular Formula: C10H16FNO4
Molecular Weight: 233.24
Purity/Analysis Method: >97.0% (GC,T)
Form: Crystal
Melting point (°C): 162
Specific rotation [a]20/D: -57 deg (C=1, MeOH)

Supplier: Enzo Life Sciences

Immunosuppressant. Isolated from Penicillium brevicompactum.

Supplier: Thermo Scientific Chemicals

A vitamin A analog that inhibits cell proliferation and induces cell differentiation

Supplier: TCI America

CAS Number: 98977-34-5
MDL Number: MFCD01862189
Molecular Formula: C13H21NO5
Molecular Weight: 271.31
Purity/Analysis Method: >97.0% (HPLC,N)
Form: Crystal
Melting point (°C): 64

Supplier: Restek

Neat fatty acid methyl esters are used to prepare specific mixtures.

Supplier: TCI America

CAS Number: 1934-21-0
MDL Number: MFCD00148908
Molecular Formula: C16H12N4O9S2
Molecular Weight: 534.36
Purity/Analysis Method: >98.0% (HPLC)
Form: Crystal
Lambda max.: 428 nm (AcONH4 sol.)

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: Bachem Americas

Sequence: H-Asp(OBzl)-OBzl · p-tosylate

Supplier: TCI America

CAS Number: 16526-68-4
MDL Number: MFCD00075294
Molecular Formula: C9H12O6
Molecular Weight: 216.19
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 218

Supplier: TCI America

CAS Number: 1936-15-8
MDL Number: MFCD00012457
Molecular Formula: C16H12N2O7S2
Molecular Weight: 452.36
Form: Crystal
Color: Reddish Yellow

Supplier: TCI America

CAS Number: 121808-62-6
MDL Number: MFCD00867583
Molecular Formula: C9H12N2O4S
Molecular Weight: 244.27
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Color: White
Melting point (°C): 187
Specific rotation [a]20/D: -136 deg (C=2, 5mol/L HCl)

Supplier: TCI America

CAS Number: 52831-11-5
Molecular Formula: C12H18O6
Molecular Weight: 258.27
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Color: White
Melting point (°C): 46

Supplier: TCI America

CAS Number: 84494-72-4
MDL Number: MFCD00056293
Molecular Formula: C24H36O2
Molecular Weight: 356.55
Purity/Analysis Method: >97.0% (GC)
Form: Clear Liquid
Specific Gravity (20/20): 0.92
Storage Temperature: 0-10°C

Supplier: TCI America

CAS Number: 2650-17-1
MDL Number: MFCD00040657
Form: Crystal
Color: Yellow Green
Lambda max.: 615 nm (H2O)

Supplier: TCI America

CAS Number: 15826-37-6
MDL Number: MFCD00057744
Molecular Formula: C23H16O11
Molecular Weight: 512.33
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal

Supplier: Proteintech

FKBP2 is also named as FKBP13 and belongs to the FKBP-type PPIase family. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides. FKBP2 has a 21-amino acid signal peptide and appears to be membrane-associated. It is localized to the lumen of the endoplasmic reticulum (ER). FKBP12 and FKBP13 are highly similar proteins, of molecular masses 12 kDa and 13 kDa respectively, with approx.43 % amino acid identity. The strong homology between FKBP12 and FKBP13 suggests that they may share similar biological functions, although, apart from rotamase activity, details relating to the function of either protein are scant.

Supplier: TCI America

CAS Number: 112-86-7
MDL Number: MFCD00063188
Molecular Formula: C22H42O2
Molecular Weight: 338.58
Purity/Analysis Method: >85.0% (GC)
Form: Crystal
Flash Point (°C): 110
Freezing point (°C): 30
Storage Temperature: 0-10°C

Supplier: TCI America

CAS Number: 1623-08-1
MDL Number: MFCD00004775
Molecular Formula: C14H15O4P
Molecular Weight: 278.24
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Color: White
Melting point (°C): 81
Storage Temperature: <0°C

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: Bioss

RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.

Supplier: TCI America

CAS Number: 140-24-9
MDL Number: MFCD00039640
Molecular Formula: C24H30O4
Molecular Weight: 382.50
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Color: White
Flash Point (°C): 232
Freezing point (°C): 27

Supplier: Proteintech

FKBP2 is also named as FKBP13 and belongs to the FKBP-type PPIase family. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides. FKBP2 has a 21-amino acid signal peptide and appears to be membrane-associated. It is localized to the lumen of the endoplasmic reticulum (ER). FKBP12 and FKBP13 are highly similar proteins, of molecular masses 12 kDa and 13 kDa respectively, with approx.43 % amino acid identity. The strong homology between FKBP12 and FKBP13 suggests that they may share similar biological functions, although, apart from rotamase activity, details relating to the function of either protein are scant.