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Other
Glycidyl Myristate
Glycidyl Myristate
United States Biological

A potential inhibitor of monoacylglycerol lipase. Form: White Low Melting Solid Solubility: Chloroform

5-Bromoindole
5-Bromoindole
United States Biological

A potential inhibitor of GSK-3 Form: Off-White Solid Melting Point: 90-92 degrees C Solubility: Chloroform, Methanol

(2S)-2-Hydroxyglutaric Acid Disodium Salt
(2S)-2-Hydroxyglutaric Acid Disodium Salt
United States Biological

A potential inhibitor of glutamate carboxypeptidase. Form: White Solid Melting Point: >300 degrees C Solubility: Water

(2R)-2-Hydroxyglutaric Acid Disodium Salt
(2R)-2-Hydroxyglutaric Acid Disodium Salt
United States Biological

A potential inhibitor of glutamate carboxypeptidase. Form: Pale Orange Solid Melting Point: >291 degrees C (dec.) Solubility: Water

4-Deoxy-D-glucose
4-Deoxy-D-glucose
United States Biological

A potential inhibitor for lactose synthase. Form: Off-White Solid Melting Point: 105-110 degrees C Solubility: Water

Iso Rizatriptan
Iso Rizatriptan
United States Biological

A potential impurity of Rizatriptan. A regioisomer of Rizatriptan. Form: White to Off-White Solid Melting Point: 96-98 degrees C Solubility: DMSO, Methanol

Rabeprazole Sulfone N-Oxide
Rabeprazole Sulfone N-Oxide
United States Biological

A potential impurity of Rabeprazole sodium. Form: Brownish Solid Melting Point: 83-85 degrees C Solubility: Chloroform, Methanol

O-Acetyl Losartan
O-Acetyl Losartan
United States Biological

A potential impurity of Losartan Form: White Solid Melting Point: 139-142 degrees C Solubility: Chloroform, Methanol

3-Dechloro-4-chloro Lamotrigine
3-Dechloro-4-chloro Lamotrigine
United States Biological

A potential impurity of Lamotrigine. Form: WHite Solid Melting Point: 230-232 degrees C Solubility: DMSO, Methanol (Sparingly)

1-(4-Acetylphenyl)-2-methyl-1-propanone
1-(4-Acetylphenyl)-2-methyl-1-propanone
United States Biological

A potential impurity in Ibuprofen Form: Light Yellow Oil Solubility: Chloroform, Ethyl Acetate

1,2,3,4-Tetrahydro-quinoline-6-ol
1,2,3,4-Tetrahydro-quinoline-6-ol
United States Biological

A potential amoebicide. Form: Off-White Solid Solubility: Methanol

AZD8055
AZD8055
United States Biological

A potent, selective, and orally bioavailable ATP-competitive mTOR kinase inhibitor with an IC50 of 0.8 nM. It inhibits the phosphorylation of mTORC1...

HZ-52
HZ-52
United States Biological

A potent, reversible inhibitor of 5-lipoxygenase, blocking leukotriene synthesis with an IC50 value of 0.7 microM in intact human polymorphonuclear...

Avridine
Avridine
United States Biological

A potent synthetic non-immunogenic adjuvant that can induce arthritis in most rat strains; immunomodulator and interferon-inducing. Form: Off-White to Pale...

2,3-Dihydro-3-(1H-indol-3-ylmethylene)-2-oxo-1H-indole-5-sulfonamide
2,3-Dihydro-3-(1H-indol-3-ylmethylene)-2-oxo-1H-indole-5-sulfonamide
United States Biological

A potent small molecule inhibitor of spleen tyrosine kinase (Syk). Form: Brownish Yellow Solid Melting Point: >300 degrees C Solubility: DMSO, Ethanol...

3,4-Cyclopentenopyrido[3,2-a]carbazole
3,4-Cyclopentenopyrido[3,2-a]carbazole
United States Biological

A potent mutagenic product from the dry distillation of L-lysine.

Oxethazaine
Oxethazaine
United States Biological

A potent local anesthetic that is active even in acidic conditions. It is used (usually in combination with an antacid) for the relief of pain associated...

Nitrosobis(2-hydroxyethyl)amine-d8
Nitrosobis(2-hydroxyethyl)amine-d8
United States Biological

A potent liver carcinogen in several species of animals, is one of the most widespread N-nitroso compounds in the human environment. Form: Yellow Oil...

Nitrosobis(2-hydroxyethyl)amine
Nitrosobis(2-hydroxyethyl)amine
United States Biological

A potent liver carcinogen in several species of animals, is one of the most widespread N-nitroso compounds in the human environment. Form: Reddish Yellow Oil...

TCS-21311
TCS-21311
United States Biological

A potent JAK3 inhibitor; selective for JAK3 over JAK1, JAK2 and TYK2. It also inhibits GSK-3b, PKCa and PKC0.

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