Chemical Formula: C11H8N2S

Chemical Formula C11H8N2S

Found 24 metabolite its formula value is C11H8N2S

Camalexin

3-(1,3-thiazol-2-yl)-1H-indole

C11H8N2S (200.0408168)


Camalexin is an indole phytoalexin that is indole substituted at position 3 by a 1,3-thiazol-2-yl group. It has a role as a metabolite. It is an indole phytoalexin and a member of 1,3-thiazoles. Camalexin is a natural product found in Arabidopsis, Arabidopsis thaliana, and Camelina sativa with data available. Camalexin is found in fats and oils. Camalexin is an alkaloid from the leaves of Camelina sativa (false flax) infected by the fungus Alternaria brassica Alkaloid from the leaves of Camelina sativa (false flax) infected by the fungus Alternaria brassicae. Camalexin is found in fats and oils. An indole phytoalexin that is indole substituted at position 3 by a 1,3-thiazol-2-yl group. D000890 - Anti-Infective Agents Camalexin is a phytoalexin isolated from Camelina sativa (Cruciferae) with antibacterial, antifungal, antiproliferative and anticancer activities. Camalexin can induce reactive oxygen species (ROS) production[1][2][3]. Camalexin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=135531-86-1 (retrieved 2024-08-14) (CAS RN: 135531-86-1). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

MTEP

2-Methyl-4-(pyridin-3-ylethynyl)thiazole

C11H8N2S (200.0408168)


   

2-Methyl-4-(pyridin-3-ylethynyl)thiazole

3-[2-(2-methyl-1,3-thiazol-4-yl)ethynyl]pyridine

C11H8N2S (200.0408168)


   

Naphtho[1,2-d]thiazol-2-amine

naphtho[1,2-d][1,3]thiazol-2-amine

C11H8N2S (200.0408168)


   

thienobenzodiazepine

5-thia-13,14-diazatricyclo[7.5.0.0^{2,6}]tetradeca-1(14),2,6,8,10,12-hexaene

C11H8N2S (200.0408168)


   

Camalexin

3-(1,3-thiazol-2-yl)-1H-indole

C11H8N2S (200.0408168)


D000890 - Anti-Infective Agents IPB_RECORD: 278; CONFIDENCE confident structure Camalexin is a phytoalexin isolated from Camelina sativa (Cruciferae) with antibacterial, antifungal, antiproliferative and anticancer activities. Camalexin can induce reactive oxygen species (ROS) production[1][2][3].

   

4-METHYL-2-PHENYLTHIAZOLE-5-CARBONITRILE

4-METHYL-2-PHENYLTHIAZOLE-5-CARBONITRILE

C11H8N2S (200.0408168)


   

3-(2-methyl-1,3-thiazol-4-yl)benzonitrile

3-(2-methyl-1,3-thiazol-4-yl)benzonitrile

C11H8N2S (200.0408168)


   

4-Thiazoleacetonitrile,2-phenyl-

4-Thiazoleacetonitrile,2-phenyl-

C11H8N2S (200.0408168)


   

2-(4-phenyl-1,3-thiazol-2-yl)acetonitrile

2-(4-phenyl-1,3-thiazol-2-yl)acetonitrile

C11H8N2S (200.0408168)


   

1H-Benzimidazole,2-(2-thienyl)-(9CI)

1H-Benzimidazole,2-(2-thienyl)-(9CI)

C11H8N2S (200.0408168)


   

6-thiophen-2-yl-1h-indazole

6-thiophen-2-yl-1h-indazole

C11H8N2S (200.0408168)


   

Imidazo[2,1-b]thiazole,6-phenyl-

Imidazo[2,1-b]thiazole,6-phenyl-

C11H8N2S (200.0408168)


   

Benzimidazole, 2- (3-thienyl)-

Benzimidazole, 2- (3-thienyl)-

C11H8N2S (200.0408168)


   

6-thiophen-3-yl-1h-indazole

6-thiophen-3-yl-1h-indazole

C11H8N2S (200.0408168)


   

PYRIDIN-2-YL-THIOPHEN-3-YL-ACETONITRILE

PYRIDIN-2-YL-THIOPHEN-3-YL-ACETONITRILE

C11H8N2S (200.0408168)


   

1H-Pyrido[3,2-b][1,4]benzothiazine

1H-Pyrido[3,2-b][1,4]benzothiazine

C11H8N2S (200.0408168)


   

1H-PYRROLO[2,3-B]PYRIDINE, 2-(2-THIENYL)-

1H-PYRROLO[2,3-B]PYRIDINE, 2-(2-THIENYL)-

C11H8N2S (200.0408168)


   

1H-Pyrrolo[2,3-b]pyridine,5-(2-thienyl)-(9CI)

1H-Pyrrolo[2,3-b]pyridine,5-(2-thienyl)-(9CI)

C11H8N2S (200.0408168)


   

5-thiophen-3-yl-1h-indazole

5-thiophen-3-yl-1h-indazole

C11H8N2S (200.0408168)


   

3-AMINO-2-CYANO-5-PHENYLTHIOPHENE

3-AMINO-2-CYANO-5-PHENYLTHIOPHENE

C11H8N2S (200.0408168)


   

4-(2-METHYLTHIAZOL-4-YL)BENZONITRILE

4-(2-METHYLTHIAZOL-4-YL)BENZONITRILE

C11H8N2S (200.0408168)


   

5-thiophen-2-yl-1h-indazole

5-thiophen-2-yl-1h-indazole

C11H8N2S (200.0408168)


   

3-Thiophen-2-ylimidazo[1,5-a]pyridine

3-Thiophen-2-ylimidazo[1,5-a]pyridine

C11H8N2S (200.0408168)