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  • DC Chemicals Limited
  • China
  • Product Name: HODHBt
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/500mg
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

28230-32-2

28230-32-2 structure
28230-32-2 structure
  • Name: HOOBT
  • Chemical Name: 3-hydroxy-1,2,3-benzotriazin-4-one
  • CAS Number: 28230-32-2
  • Molecular Formula: C7H5N3O2
  • Molecular Weight: 163.133
  • Catalog: Biochemical Condensing agent
  • Create Date: 2018-12-02 19:04:19
  • Modify Date: 2024-01-02 11:30:29
  • HODHBt (HOOBt) inhibits STAT5-SUMO interaction by blocking SUMOylation of phosphorylated STAT5. HODHBt enhances the magnitude of IL-15 signaling and significantly increases the natural killer (NK) cell cytotoxicity phenotype and function and the generation of cytokine-induced memory-like (CIML) natural killer (NK) cells. HODHBt can be used for research of HIV-infection and cancer[1].

Name 3-hydroxy-1,2,3-benzotriazin-4-one
Synonyms HOOBT
EINECS 248-916-1
3-hydroxybenzo[d]1,2,3-triazin-4-one
3-hydroxy-3H-benzo[d][1,2,3]triazin-4-one
1,2,3-Benzotriazin-4(3H)-one, 3-hydroxy-
DHBT
oxohydroxybenzotriazole
4-oxo-3,4-dihydro-3-hydroxy-1,2,3-benzotriazine
3-Hydroxy-1,2,3-benzotriazin-4(3H)-one
3-Hydroxy-4-ketobenzotriazine
3-Hydroxy-1,2,3-ben zotriazin-4(3H)-one
3,4-Dihydro-3-hydroxy-4-oxo-1,2,3-benzotriazine
1,2,3-Benzotriazin-4(3H)-one,3-hydroxy
MFCD00042803
3,4-dihydro-3-hydroxy-4-keto-1,2,3-benzotriazine
3-Hydroxy-3,4-dihydro-4-oxo-1,2,3-benzotriazine
Description HODHBt (HOOBt) inhibits STAT5-SUMO interaction by blocking SUMOylation of phosphorylated STAT5. HODHBt enhances the magnitude of IL-15 signaling and significantly increases the natural killer (NK) cell cytotoxicity phenotype and function and the generation of cytokine-induced memory-like (CIML) natural killer (NK) cells. HODHBt can be used for research of HIV-infection and cancer[1].
Related Catalog
Target

STAT5

In Vitro HODHBt (100 μM; 24 h, and 48 h respectively) increases IL-15-mediated STAT phosphorylation in NK cells and enhances the cytotoxic profile of NK cells[1]. HODHBt (100 μM; 24 h) enhances IL-15-mediated (100 ng/mL) cytotoxicity of NK cells against HIV-infected cells (K562 cells)[1]. HODHBt (100 μM; 24 h) enhances IL-15-mediated (100 ng/mL, 6 h) cytotoxicity of NK cells against cancer cell lines (A2780 and U877; OCILy1 and OCILy10)[1]. HODHBt (100 μM; 7 d) results in enhanced memory response upon recall in generation of human CIML NK cells in vitro[1].
Density 1.6±0.1 g/cm3
Boiling Point 348.7±25.0 °C at 760 mmHg
Melting Point 184-189°C
Molecular Formula C7H5N3O2
Molecular Weight 163.133
Flash Point 164.7±23.2 °C
Exact Mass 163.038177
PSA 68.01000
LogP 0.43
Vapour Pressure 0.0±0.8 mmHg at 25°C
Index of Refraction 1.739
Storage condition 2-8°C
Symbol GHS02 GHS07 GHS08
GHS02, GHS07, GHS08
Signal Word Danger
Hazard Statements H226-H312 + H332-H315-H319-H335-H360D
Precautionary Statements P201-P261-P280-P305 + P351 + P338-P308 + P313
Personal Protective Equipment Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes Xi:Irritant
Risk Phrases R36/37/38
Safety Phrases S53-S26-S35-S36/37-S45-S37/39
RIDADR UN 3379 3/PG 1
WGK Germany 3
Hazard Class 3.0
HS Code 2933699090

~77%

28230-32-2 structure

28230-32-2

Literature: FRUTAROM LTD. Patent: WO2005/7634 A1, 2005 ; Location in patent: Page 39 ;

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28230-32-2 structure

28230-32-2

Literature: Jakobsen, Mogens Havsteen; Buchardt, Ole; Holm, Arne; Meldal, Morten Synthesis, 1990 , # 11 p. 1008 - 1010

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28230-32-2 structure

28230-32-2

Literature: Vaughan, Keith; Wilman, Derry E. V.; Wheelhouse, Richard T.; Stevens, Malcolm F. G. Magnetic Resonance in Chemistry, 2002 , vol. 40, # 4 p. 300 - 302
HS Code 2933699090
Summary 2933699090 other compounds containing an unfused triazine ring (whether or not hydrogenated) in the structure。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:20.0%