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Details

Stereochemistry ACHIRAL
Molecular Formula C40H30N10O6.2Cl
Molecular Weight 817.636
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NITROBLUE TETRAZOLIUM CHLORIDE

SMILES

[Cl-].[Cl-].COC1=C(C=CC(=C1)C2=CC(OC)=C(C=C2)[N+]3=NC(=NN3C4=CC=C(C=C4)[N+]([O-])=O)C5=CC=CC=C5)[N+]6=NC(=NN6C7=CC=C(C=C7)[N+]([O-])=O)C8=CC=CC=C8

InChI

InChIKey=FSVCQIDHPKZJSO-UHFFFAOYSA-L
InChI=1S/C40H30N10O6.2ClH/c1-55-37-25-29(13-23-35(37)47-43-39(27-9-5-3-6-10-27)41-45(47)31-15-19-33(20-16-31)49(51)52)30-14-24-36(38(26-30)56-2)48-44-40(28-11-7-4-8-12-28)42-46(48)32-17-21-34(22-18-32)50(53)54;;/h3-26H,1-2H3;2*1H/q+2;;/p-2

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
MOL RATIO 2 MOL RATIO (average)
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C40H30N10O6
Molecular Weight 746.7296
Charge 2
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description

Nitroblue Tetrazolium (NBT) is a chromogenic substrate that, like other tetrazolium compounds, can be reduced to produce a colored formazan derivative. Conventionally, a semi-quantitative microscopic NBT assay is used to determine the production of superoxide anion (O2(-)) in various phagocytic cells. This microscopic assay is conducted by counting the cells containing blue NBT formazan deposits, which are formed by reduction of the membrane permeable, water-soluble, yellow-colored, nitroblue tetrazolium (Y-NBT) by O2(-). NBT test, the oldest and most recognized diagnostic test for chronic granulomatous disease (CGD), relies on light microscopy to provide a mostly qualitative determination of phagocyte NADPH oxidase activity: production of blue reduced NBT formazan in normal cells but not in those from patients with CGD. NBT can also be used as a chromogenic activity stain for oxidoreductases in gels or solutions. More commonly NBT is often paired with 5-bromo-4-chloro-3-inolyl phosphate (PCIB) for the colorimetric detection of alkaline phosphatase activity. Alkaline phosphate converts PCIB to a product that reduces NBT to its formazan derivative, resulting in a black-purple precipitate.

Approval Year

Targets

Primary TargetPharmacologyConditionPotency

Conditions

ConditionModalityTargetsHighest PhaseProduct
Diagnostic
Nitroblue tetrazolium (NBT) test

PubMed

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Technique for the performance of the nitro-blue tetrazolium (NBT) test. Blood is obtained in glass tubes, using heparin as anticoagulant (the concentration of heparin should be 75-100 units/ml of blood). The usual amounts of blood required from the patient is never more than 10 ml. Pipette 0 1 ml of the blood into a well of the plastic tray. Make the 'working' NBT solution by mixing equal volumes of the stock 0.2 % solution and the phosphate-buffered saline. This solution must be made freshly for each batch of tests. Pipette 0.1 ml of the 'working' NBT solution into each well containing blood and mix the contents. Cover the tray with another tray to ensure humidity, and incubate at 37°C for 15 minutes. Follow this with an equal period at room temperature. Using a Pasteur pipette, or a large bacteriological loop, with which to transfer the blood-NBT mixture, make careful coverslip smears and allow them to dry in air. Fix the smears in methanol for three minutes. Stain with Pappenheim's stain for three to five minutes. (The actual time is best decided by trial, the desired result being to stain the granulocyte nuclei green and to leave most of the erythrocytes as 'ghosts'). Air dry and mount in DePeX. Examine under the 40 x objective and assess the number of neutrophils containing the formazan deposit as a percentage.
Substance Class Chemical
Record UNII
X44P41F7ZK
Record Status Validated (UNII)
Record Version