accessibility menu, dialog, popup

UserName
Viewing profile as user:

Nitrophenols

Organic compounds derived from phenols that contain a nitro functional group (-NO2).
Molecular Weight (g/mol) 
  • (2)
  • (1)
Quantity 
  • (1)
  • (1)
  • (1)
Percent Purity 
  • (2)

Filtered Search Results

Products from some of our suppliers do not display in filtered search results. Please clear all filters to see these products.

Narrow Results

Narrow Results

category

brands

  • (2)
  • (10)
  • (7)
  • (3)

special interests

  • (13)

Molecular Weight (g/mol)

  • (2)
  • (1)

Quantity

  • (1)
  • (1)
  • (1)

Percent Purity

  • (2)
Search Within Results
Keyword Search:
1 – 15 of 22 results
1

Sigma Aldrich methyldodecylbenzyl trimethyl ammonium chloride

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

ENCOMPASS
2

Sigma Aldrich 3,5-Dinitrosalicylic acid

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

ENCOMPASS
Percent Purity 98%
Linear Formula (O2N)2C6H2-2-(OH)CO2H
CAS 609-99-4
Molecular Weight (g/mol) 228.12
MDL Number MFCD00007104
Synonym 3,5-Dinitro-2-hydroxybenzoic acid; DNS
RTECS Number VO2965000
Recommended Storage Room Temperature
Molecular Formula C7H4N2O7
EINECS Number 210-204-3
Melting Point 168°C to 172°C (lit.)
3

Selleck Chemical LLC FHD-609-E1859-5MG

FHD-609 acts as a selective inhibitor and degrader of BRD9 protein (bromodomain-containing protein 9) FHD-609 targets ncBAF and can be used in research of various cancers involving mutations in a BAF complex subunit

ENCOMPASS_PREFERRED
4

Selleck Chemical LLC FHD-609-E1859-1G

FHD-609 acts as a selective inhibitor and degrader of BRD9 protein (bromodomain-containing protein 9) FHD-609 targets ncBAF and can be used in research of various cancers involving mutations in a BAF complex subunit

ENCOMPASS_PREFERRED
5

Selleck Chemical LLC FHD-609-E1859-25MG

FHD-609 acts as a selective inhibitor and degrader of BRD9 protein (bromodomain-containing protein 9) FHD-609 targets ncBAF and can be used in research of various cancers involving mutations in a BAF complex subunit

ENCOMPASS_PREFERRED
6

Selleck Chemical LLC FHD-609-E1859-100MG

FHD-609 acts as a selective inhibitor and degrader of BRD9 protein (bromodomain-containing protein 9) FHD-609 targets ncBAF and can be used in research of various cancers involving mutations in a BAF complex subunit

ENCOMPASS_PREFERRED
7

Medchemexpress LLC STO-609 | 52029-86-4 | 98.2% | 314.29 | 100 MG
SDP

STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK), with Ki values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively. It inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates with an IC50 ~0.02 g/ml.

  • Selective inhibitor of CaM-KK
  • Cell-permeable
  • Inhibits AMPKK activity

ENCOMPASS_PREFERRED
8

Medchemexpress LLC FHD-609 | 2676211-64-4 | C47H56N8O6 | 250 MG
SDP

FHD-609 is a PROTAC degrader and inhibitor of BRD9 (Bromodomain-containing protein 9). It targets ncBAF and is used for research in various cancers with mutations in a BAF complex subunit. It may also play a role in adrenocortical carcinoma (ACC) treatment when combined with Telomelysin or INO5401.

  • Targets BRD9 (Bromodomain-containing protein 9)
  • Functions as a PROTAC degrader and inhibitor
  • Useful for research on various cancers with BAF complex subunit mutations
  • Shows anti-tumor activities in vivo
  • High purity of 98.95%
  • Appearance is solid, white to off-white

ENCOMPASS_PREFERRED
9

Selleck Chemical LLC STO-609

STO-609 is a specific inhibitor of the Ca2 /Calmodulin-dependent protein kinase kinase(CaM-KK) that inhibits the activities of recombinant CaM-KK and CaM-KK isoforms with Ki values of 80 and 15 ng/ml respectively and also inhibits their autophosphorylation activities STO-609 inhibits AMPKK activity and inhibits autophagy

ENCOMPASS_PREFERRED
10

Selleck Chemical LLC STO-609

STO-609 is a specific inhibitor of the Ca2 /Calmodulin-dependent protein kinase kinase(CaM-KK) that inhibits the activities of recombinant CaM-KK and CaM-KK isoforms with Ki values of 80 and 15 ng/ml respectively and also inhibits their autophosphorylation activities STO-609 inhibits AMPKK activity and inhibits autophagy

ENCOMPASS_PREFERRED
11

Selleck Chemical LLC STO-609

STO-609 is a specific inhibitor of the Ca2 /Calmodulin-dependent protein kinase kinase(CaM-KK) that inhibits the activities of recombinant CaM-KK and CaM-KK isoforms with Ki values of 80 and 15 ng/ml respectively and also inhibits their autophosphorylation activities STO-609 inhibits AMPKK activity and inhibits autophagy

ENCOMPASS_PREFERRED
12

Medchemexpress LLC FHD-609 | 2676211-64-4 | C47H56N8O6 | 1 G
SDP

FHD-609 is a PROTAC degrader and inhibitor of BRD9 (Bromodomain-containing protein 9). It targets ncBAF and can be used for research on a wide range of cancers that contain a mutation in a BAF complex subunit. When combined with Telomelysin or INO5401, FHD-609 may have a role in adrenocortical carcinoma (ACC) treatment.

  • PROTAC degrader and inhibitor of BRD9 (Bromodomain-containing protein 9).
  • Targets ncBAF.
  • Applicable for research into cancers with a mutation in a BAF complex subunit.
  • Potential for adrenocortical carcinoma (ACC) treatment in combination with Telomelysin or INO5401.
  • Purity: 98.95%.
  • Molecular weight: 829.00.
  • Formula: C47H56N8O6.
  • Appearance: Solid, white to off-white.

ENCOMPASS_PREFERRED
13

Medchemexpress LLC Sto-609 | 52029-86-4 | 98.20% | 314.29 | 50 MG
SDP

STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK). It inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates with an IC50 of approximately 0.02 g/ml. It is highly selective for CaM-KK without significant effect on downstream CaM kinases.

  • Inhibits recombinant CaM-KKα and CaM-KKβ isoforms and their autophosphorylation activities.
  • Has an IC50 value against CaM-KII of 10 μg/mL.
  • Inhibits constitutively active CaM-KKα and wild-type enzyme.
  • Suppresses Ca2+-induced activation of CaM-KIV in a dose-dependent manner in transfected HeLa cells.
  • Reduces endogenous activity of CaM-KK in SH-SY5Y neuroblastoma cells at 1μg/mL (80% inhibitory rate).

ENCOMPASS_PREFERRED
14

Medchemexpress LLC STO-609 | 52029-86-4 | 98.2% | 314.29 | 1 ML
SDP

STO-609 is a selective and cell-permeable inhibitor of Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK), exhibiting Ki values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively. It inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates (IC50 ~0.02 g/ml) and is highly selective for CaM-KK, with no significant effect on downstream CaM-KI and -IV. It also inhibits both constitutively active and wild-type CaM-KKα, and suppresses Ca2+-induced activation of CaM-KIV. The inhibition mechanism is ATP-competitive.

  • Selective and cell-permeable CaM-KK inhibitor.
  • Inhibits AMPKK activity.
  • High selectivity for CaM-KK.
  • Suppresses Ca2+-induced activation of CaM-KIV.
  • ATP-competitive inhibition mechanism.

ENCOMPASS_PREFERRED
15

TARGETMOL CHEMICALS INC STO-609 10MG
SDP

Also available in 1 mL, 1 mg, 5 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. STO-609 is a specific and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK) for recombinant CaM-KKalpha/KKbeta (Ki 80/15 ng/mL). Purity 98.95%

ENCOMPASS_PREFERRED