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There is one exact (name or code) match for sulfaphenazole

SULFAPHENAZOLE

0J8L4V3F81

Search for Structure

Status:

US Previously Marketed

Source:

SULFABID by PURDUE FREDERICK

(1963)

Source URL:

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=013092

First approved in 1963

Source:

SULFABID by PURDUE FREDERICK

Source URL:

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=013092

Class (Stereo):

CHEMICAL (ACHIRAL)

Targets:

Bacterial dihydropteroate synthase

Conditions:

Bacterial infections

Sulfaphenazole is an oral antibiotic, which was used for the treatment of bacterial infections under the name Sulfabid. The drug was found to block folate synthesis in bacterias by inhibiting the enzyme dihydropteroate synthase. Sulfaphenazole is also known to inhibit CYP2C9 with high potency and specificity. Sulfabid is no longer marketed in the USA.

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SULFAPHENAZOLE

0J8L4V3F81

Search for Structure

Status:

US Previously Marketed

Source:

SULFABID by PURDUE FREDERICK

(1963)

Source URL:

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=013092

First approved in 1963

Source:

SULFABID by PURDUE FREDERICK

Source URL:

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=013092

Class (Stereo):

CHEMICAL (ACHIRAL)

Targets:

Bacterial dihydropteroate synthase

Conditions:

Bacterial infections

Sulfaphenazole is an oral antibiotic, which was used for the treatment of bacterial infections under the name Sulfabid. The drug was found to block folate synthesis in bacterias by inhibiting the enzyme dihydropteroate synthase. Sulfaphenazole is also known to inhibit CYP2C9 with high potency and specificity. Sulfabid is no longer marketed in the USA.

Structure of SULFAPHENAZOLE

ACHIRAL

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