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Benzothiadiazoles

Organic heterocyclic compounds that consist of a benzene fused with a thiadiazole ring; thiadiazoles have a five-membered ring that contains two nitrogen atoms, one sulfur atoms, and two double bonds.
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Physical Form 
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Molecular Weight (g/mol)

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Physical Form

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Boiling Point

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Search Within Results
Keyword Search:
76 – 90 of 107 results
76

Chemscene ChemScene | 4-Bromobenzo[c][1,2,5]thiadiazole | 5G | CS-W018450 | 0.98 | 22034-13-5| MFCD00614355 | 215.07

ChemScene | 4-Bromobenzo[c][1,2,5]thiadiazole | 5G | CS-W018450 | 0.98 | 22034-13-5| MFCD00614355 | 215.07

ENCOMPASS_PREFERRED
77

Ambeed AMBEED

5000892269 3-CHLORO-124-THIADIAZOL-5 50MG

ENCOMPASS_PREFERRED
78

Ambeed AMBEED

5000895299 124-THIADIAZOL-3-AMINE 250MG

ENCOMPASS_PREFERRED
79

Medchemexpress LLC PSB-22034 100 mg
SDP

PSB-22034 100MG

ENCOMPASS_PREFERRED
80

TARGETMOL CHEMICALS INC PI-273 10MG

Also available in 1 mg, 5 mg, 25 mg, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. PI-273, a Substrate-Competitive, Specific Small-Molecule Inhibitor of PI4KIIalpha, Inhibits the Growth of Breast Cancer Cells Purity 98.04%

ENCOMPASS_PREFERRED
81

Medchemexpress LLC 2 1 3-BENZOTHIADIAZO 250 mg
SDP

2 1 3-BENZOTHIADIAZO 250MG

ENCOMPASS_PREFERRED
82

Ambeed AMBEED

5000891732 7-BROMO-213-BENZOTHIADIA 100MG

ENCOMPASS_PREFERRED
83

Medchemexpress LLC S-[2-[6-[[4-[3-(dimethylamino)propoxy]phenyl]sulfonylamino]-3-pyridinyl]-2-oxoethyl] ethanethioate | 940943-37-3 | MFCD19690928 | 98.1% | 451.56 g·mol⁻¹ | C20H25N3O5S2 | 25 MG
SDP

KD 5170 is a mercaptoketone-based pan inhibitor of histone deacetylases (HDACs) that demonstrates broad-spectrum antitumor activity in vitro and in vivo. It is supplied as a white to yellow solid for research use only.

  • Potent pan-histone deacetylase (HDAC) inhibition.
  • Demonstrated broad-spectrum antitumor activity in vitro and in vivo.
  • High reported purity (≈98.1%).
  • Available in small-mass pack sizes suitable for preclinical studies.
  • White to yellow solid form, convenient for storage and handling.
  • Intended for research use only and not for human therapeutic use.

ENCOMPASS_PREFERRED
84

eMolecules​ 352018-95-2 | 4-IODO-2,1,3-BENZOTHIADIAZOLE | AstaTech | MFCD02681904 | 262.070 | C6H3IN2S | 95.000 | Ic1cccc2nsnc12 | 5g | 277517082

4-IODO-2,1,3-BENZOTHIADIAZOLE | AstaTech | 352018-95-2 | MFCD02681904 | 262.070 | C6H3IN2S | 95.000 | Ic1cccc2nsnc12 | 5g | 277517082

ENCOMPASS_PREFERRED
85

Accela Chembio Inc 2 | 1 | 3-benzothiadiazole | 100g | 273-13-2 | MFCD00005809 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4
SDP

2 | 1 | 3-benzothiadiazole | 100g | 273-13-2 | MFCD00005809 | 97+% | Shelf Life: 1260 Days | Light Sensitive/+4

ENCOMPASS_PREFERRED
86

Ambeed AMBEED

5000870499 METHYL 213-BENZOTHIADIAZOL 1GR

ENCOMPASS_PREFERRED
87

Chemscene ChemScene | 4,7-Dibromo-2,1,3-benzothiadiazole | 10G | CS-W002651 | 0.98 | 15155-41-6| MFCD00658844 | 293.97

ChemScene | 4,7-Dibromo-2,1,3-benzothiadiazole | 10G | CS-W002651 | 0.98 | 15155-41-6| MFCD00658844 | 293.97

ENCOMPASS_PREFERRED
88

Medchemexpress LLC FAUC 213 | 337972-47-1 | 99.9% | C18H19ClN4 | 50 MG
SDP

FAUC 213 is an orally active and highly selective dopamine D4 receptor complete antagonist with a Ki of 2.2 nM for hD4.4. It shows less activity on D2 and D3 receptors, with Kis of 3.4 μM and 5.3 μM respectively. This compound can cross the blood-brain barrier (BBB) and exhibits atypical antipsychotic characteristics.

  • Highly selective dopamine D4 receptor complete antagonist
  • Orally active
  • Crosses the blood-brain barrier (BBB)
  • Exhibits atypical antipsychotic characteristics
  • Inhibits p5-HT1 (Ki=1.2 μM), p5-HT2 (Ki=0.52 μM), and pα1 (Ki=0.27 μM)
  • Significantly reduces amphetamine-induced locomotor hyperactivity at 30 mg/kg
  • Restores prepulse inhibition reduction caused by apomorphine treatment at 30 mg/kg

ENCOMPASS_PREFERRED
89

Medchemexpress LLC MEDCHEMEXPRESS LLC
SDP

5000759837 2 1 3-BENZOTHIADIAZO 100MG

ENCOMPASS_PREFERRED
90

Medchemexpress LLC XOMA-213 5 mg
SDP

XOMA-213 5MG

ENCOMPASS_PREFERRED