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United States Biological

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D-Phenylglycinol
D-Phenylglycinol
United States Biological

A chiral arylalkylamine used as organocatalysts. Used in the synthesis and chiral recognition properties of novel fluorescent chemosensors for amino acid....

DL-Phenylglycinol
DL-Phenylglycinol
United States Biological

A chiral arylalkylamine used as organocatalysts. Used in the synthesis and chiral recognition properties of novel fluorescent chemosensors for amino acid....

Nelarabine
Nelarabine
United States Biological

A chemotherapy drug used in the treatment of relapsed/refractory T-cell acute lymphoblastic leukemia (T-ALL) and T-cell lymphoblastic lymphoma (T-LBL).

Evodiamine
Evodiamine
United States Biological

A chemical extracted from Evodia plants, and has been shown to reduce fat uptake. Form: Pale Yellow Solid Melting Point: >240 degrees C (dec.) Solubility:...

4-Phenylbutyric Acid
4-Phenylbutyric Acid
United States Biological

A chemical chaperone involved in protein-folding disorders. Form: Off-White Solid Melting Point: 50-52 degrees C Solubility: Chloroform, Methanol

Dibromocyanoacetamide
Dibromocyanoacetamide
United States Biological

A chemical additive to control bacterial contamination in ethanol fermentation. Form: White Solid Melting Point: 120-122 degrees C Solubility: DMSO, Methanol

1,10-Phenanthroline
1,10-Phenanthroline
United States Biological

A chelating agent, forming complexes with most metal ions. Form: Off- White Solid Melting Point: 110-112 degrees C Solubility: Chloroform, Ethyl Acetate

(2S,3R,4E)-2-Butyrylamino-4-decene-1,3-diol
(2S,3R,4E)-2-Butyrylamino-4-decene-1,3-diol
United States Biological

A ceramide derivative used as a compound for the development of antiallergic agents. Form: White Solid Melting Point: 59-61 degrees C Solubility: Chlorform,...

Cefacetrile
Cefacetrile
United States Biological

A cephalosporin antibiotic. Form: Pale Beige Solid Melting Point: 133-135 degrees C Solubility: DMSO, Methanol

Cefdinir ((6R,7R)-7-[[(2Z)-(2-Amino-4-thiazolyl)(hydroxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid)
Cefdinir ((6R,7R)-7-[[(2Z)-(2-Amino-4-thiazolyl)(hydroxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid)
United States Biological

A Cephalosporin antibiotic structurally similar to Cefixime. Melting Point: >215 degrees C (decomposes) Solubility: Methanol (sparingly); DMSO Method for...

Clofedanol Hydrochloride
Clofedanol Hydrochloride
United States Biological

A centrally-acting cough suppressant. It has local anesthetic and antihistamine properties, and may have anticholinergic effects at high doses.

Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2 (1,3-Dihydro-1-(1-((4-(6-phenyl-1H-imidazo[4,5-g]quinoxalin-7-yl)phenyl)methyl)-4-piperidinyl)-2H-benzimidazol-2-one, Akti-1/2)
Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2 (1,3-Dihydro-1-(1-((4-(6-phenyl-1H-imidazo[4,5-g]quinoxalin-7-yl)phenyl)methyl)-4-piperidinyl)-2H-benzimidazol-2-one, Akti-1/2)
United States Biological

A cell-permeable, reversible, potent, and selective inhibitor of Akt1/Akt2 activity (IC50=58nM, 210nM, and 2.12uM for Akt1, Akt2, and Akt3, respectively, in...

Caspase Inhibitor I (Z-VAD (OMe)-FMK)
Caspase Inhibitor I (Z-VAD (OMe)-FMK)
United States Biological

A cell-permeable, irreversible, pan-caspase inhibitor. Shown to enhance the freeze-thaw survival of human embryonic stem cells. Inhibits Fas-mediated...

AMPK Inhibitor, Compound C (6-[4-(2-Piperidin-1-yl-ethoxy)-phenyl)]-3-pyridin-4-yl-pyrrazolo[1,5-a]-pyrimidine, Dorsomorphin, BMP Inhibitor I)
AMPK Inhibitor, Compound C (6-[4-(2-Piperidin-1-yl-ethoxy)-phenyl)]-3-pyridin-4-yl-pyrrazolo[1,5-a]-pyrimidine, Dorsomorphin, BMP Inhibitor I)
United States Biological

A cell-permeable pyrrazolopyrimidine compound that inhibits against KDR/VEGFR2, ALK2/BMPR-I, AMPK kinase activity (IC50=25.1, 148, and 234.6 nM,...

Rac1 Inhibitor (NSC23766)
Rac1 Inhibitor (NSC23766)
United States Biological

A cell-permeable pyrimidine compound that specifically and reversibly inhibits Rac1 GDP/GTP exchange activity by interfering with the interaction between...

Rho Kinase Inhibitor (H-1152, H-1152P, (S)-(+)-2-Methyl-1-[(4-methyl-5-isoquinolinyl)sulfonyl]homopiperazine, 2HCl, ROCK Inhibitor)
Rho Kinase Inhibitor (H-1152, H-1152P, (S)-(+)-2-Methyl-1-[(4-methyl-5-isoquinolinyl)sulfonyl]homopiperazine, 2HCl, ROCK Inhibitor)
United States Biological

A cell-permeable isoquinolinesulfonamide compound that acts as a highly specific, reversible, potent, and ATP-competitive inhibitor of G-protein...

3-(4-Pyridyl)indole
3-(4-Pyridyl)indole
United States Biological

A cell-permeable indolopyridine compound that acts as a selective, ATP-competitive inhibitor of Rho kinase (ROCK) activity. Form: Yellow Solid Solubility:...

Zinpyr-4
Zinpyr-4
United States Biological

A cell-permeable fluorescent probe selective for Zinc. Fluorescence: max. Em. l = 515nm Form: Orange Powder Solubility: Dichloromethane, DMSO, Ethanol

Secretase, gamma Inhibitor IX (DAPT N-[N-(3,5-Difluorophenacetyl-L-alanyl)]-S-phenylglycine t-Butyl Ester)
Secretase, gamma Inhibitor IX (DAPT N-[N-(3,5-Difluorophenacetyl-L-alanyl)]-S-phenylglycine t-Butyl Ester)
United States Biological

A cell-permeable dipeptide that inhibits y-secretase activity and suppresses Ab production (Ab total IC50=115nM; Ab42 IC50=200nM). Reported to be...

Kinetin
Kinetin
United States Biological

A cell division factor found in various plant parts and in yeast. A plant growth regulator. Augments growth of microbial cultures. Form: White Solid Melting...

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