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6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt)
6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt)
CAS No. 138182-20-4
6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt)( —— )
Catalog No. M28148 CAS No. 138182-20-4
6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) is a chromogenic substrate for β-glucuronidase. 6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) can be used in the histochemical analysis of β-glucuronidase activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
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| 10MG | 29 | In Stock |
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| 25MG | 46 | In Stock |
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| 50MG | 63 | In Stock |
|
| 100MG | 96 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 216 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product Name6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt)
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NoteResearch use only, not for human use.
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Brief Description6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) is a chromogenic substrate for β-glucuronidase. 6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) can be used in the histochemical analysis of β-glucuronidase activity.
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Description6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) is a chromogenic substrate for β-glucuronidase. 6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) can be used in the histochemical analysis of β-glucuronidase activity.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorMALT1|Apoptosis
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Research Area——
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Indication——
Chemical Information
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CAS Number138182-20-4
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Formula Weight442.89
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Molecular FormulaC20H27ClN2O7
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Purity>98% (HPLC)
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Solubility——
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SMILESNC1CCCCC1.O[C@@H]1[C@@H](O)[C@H](Oc2c[nH]c3cc(Cl)ccc23)O[C@@H]([C@H]1O)C(O)=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Nagel D, et al. Pharmacologic inhibition of MALT1 protease by phenothiazines as a therapeutic approach for the treatment of aggressive ABC-DLBCL. Cancer Cell. 2012 Dec 11;22(6):825-37.
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