K1003

Ketoconazole

99.0-101.0% (EP, titration)

Manufacturer: Sigma Aldrich

CAS Number: 65277-42-1

Synonym(S): (±)-cis-1-Acetyl-4-(4-[(2-[2,4-dichlorophenyl]-2-[1H-imidazol-1-ylmethyl]-1,3-dioxolan-4-yl)-methoxy]phenyl)piperazine

Select a Size

Pack Size SKU Availability Price
100 MG K1003-100-MG In Stock ₹ 21,834.03

K1003 - 100 MG

₹ 21,834.03

In Stock

Quantity

1

Base Price: ₹ 21,834.03

GST (18%): ₹ 3,930.125

Total Price: ₹ 25,764.155

description

Specific Optical Rotation (EP): (−0.10) ∼ +0.10 °

Quality Level

200

Assay

99.0-101.0% (EP, titration)

form

powder

color

white to off-white

antibiotic activity spectrum

Gram-positive bacteriafungiyeast

Mode of action

enzyme | inhibits

storage temp.

2-8°C

SMILES string

CC(=O)N1CCN(CC1)c2ccc(OC[C@H]3CO[C@@](Cn4ccnc4)(O3)c5ccc(Cl)cc5Cl)cc2

InChI

1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3/t23-,26-/m0/s1

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Description

  • General description: Chemical structure: imidazole
  • Application: Ketoconazole is a broad spectrum antifungal agent used to treat candidiasis, chronic mucocutaneous candidiasis, oral thrush, candiduria, blastomycosis, coccidioidomycosis, histoplasmosis, chromomycosis, and paracoccidioidomycosis. It is used to identify p-glycoprotein/CYP3A-limited bioavailability in the monkey model[1], to study interleukin 1 mediated antitumor effects[2], and drug interactions in vivo[3]
  • Biochem/physiol Actions: Ketoconazole interacts with 14-α demethylase, a cytochrome P-450 enzyme that is necessary for the conversion of lanosterol to ergosterol. This interaction inhibits ergosterol synthesis and results in increased fungal cellular permeability. Other possible mechanisms of action are the inhibition of endogenous respiration, interaction with membrane phospholipids, inhibition of yeast transformation to mycelial forms, inhibition of purine uptake, and impairment of triglyceride and/or phospholipid biosynthesis. Ketoconazole inhibits the synthesis of thromboxane and sterols such as aldosterone, cortisol, and testosterone .

SAFETY INFORMATION

Pictograms

GHS06,GHS08,GHS09

Signal Word

Danger

Hazard Statements

H301,H360F,H373,H410

Precautionary Statements

P202 - P260 - P264 - P273 - P280 - P301 + P310

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - STOT RE 2

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves