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KPC Pharmaceuticals, Inc.
  • Founded in:

    1995-12-14
  • Country:

    China China
  • Address:

    No. 166, Keyi Road, High-tech Industrial Development Zone, Kunming, Yunnan Province
  • Tax NO.:

    91530000216562280W
  • Registered Funds:

    757.986969 yuan
  • Website:

  • Email:

Related Drugs
Hexamethylenetetramine tablets
The main ingredient of this product is methenamine.
Name Description Content CAS NO. Registered Holders
Hexamethylenetetramine

After oral absorption, this product slowly decomposes into formaldehyde and ammonia in acidic urine. Formaldehyde has a bactericidal effect. Ammonia can easily alkalinize urine, so it is necessary to take acidifying urine drugs such as ammonium chloride when taking it.

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After oral absorption, this product slowly decomposes into formaldehyde and ammonia in acidic urine. Formaldehyde has a bactericidal effect. Ammonia can easily alkalinize urine, so it is necessary to take acidifying urine drugs such as ammonium chloride when taking it.

0
Hexamethylenetetramine tablets
The main ingredient of this product is methenamine.
Name Description Content CAS NO. Registered Holders
Hexamethylenetetramine

After oral absorption, this product slowly decomposes into formaldehyde and ammonia in acidic urine. Formaldehyde has a bactericidal effect. Ammonia can easily alkalinize urine, so it is necessary to take acidifying urine drugs such as ammonium chloride when taking it.

More

After oral absorption, this product slowly decomposes into formaldehyde and ammonia in acidic urine. Formaldehyde has a bactericidal effect. Ammonia can easily alkalinize urine, so it is necessary to take acidifying urine drugs such as ammonium chloride when taking it.

0
Epinephrine Hydrochloride Injection
The chemical name of this product is: (R)-4[2-(methylamino)-1-hydroxyethyl]-1,2-benzenediol hydrochloride. Molecular formula: C9H13NO3HCl Molecular weight: 219.67
Name Description Content CAS NO. Registered Holders
Epinephrine Hydrochloride

It has both α-receptor and β-receptor stimulating effects. Alpha-receptor stimulating causes vasoconstriction of the skin, mucous membranes, and visceral vessels. β-receptor stimulating causes coronary vasodilation, skeletal muscle, myocardial excitation, increased heart rate, and relaxation of bronchial smooth muscle and gastrointestinal smooth muscle. The effect on blood pressure is dose-related. Common doses increase systolic blood pressure while diastolic blood pressure does not increase or decreases slightly. High doses increase both systolic and diastolic blood pressure.

More

It has both α-receptor and β-receptor stimulating effects. Alpha-receptor stimulating causes vasoconstriction of the skin, mucous membranes, and visceral vessels. β-receptor stimulating causes coronary vasodilation, skeletal muscle, myocardial excitation, increased heart rate, and relaxation of bronchial smooth muscle and gastrointestinal smooth muscle. The effect on blood pressure is dose-related. Common doses increase systolic blood pressure while diastolic blood pressure does not increase or decreases slightly. High doses increase both systolic and diastolic blood pressure.

55-31-2 0
Etoposide
Chemical name: 4'-demethyl epipodophyllotoxin-beta;-D-ethylidene pyranoglucoside (-)-(5R, 5aR, 8aR, as)-a-[(4,6,-O-CR)-ethylidene-beta;-D-pyranoglucoside]oxy]-5,8,8a,9-tetrahydro-5-(4-hydroxy, 5-dimethoxyphenyl)furan[3`,4`:6,7]naphtho[2,3-d]-1,3-e9dioxo-6(5aH)-one. Molecular formula: C29H32O13.
Name Description Content CAS NO. Registered Holders
Etoposide

Etoposide is an effective component of lignans isolated from podophyllin. VP-16 is a cell cycle-specific anti-tumor drug that acts in the late S phase or G2 phase. Its action site is topoisomerase II, forming a stable cleavable complex between drug, enzyme and DNA, interfering with DNA topoisomerase II, making the damaged DNA unable to be repaired. By stabilizing the DNA breakage complex, it causes double-line breaks in DNA and topoisomerase II. It activates certain endonucleases in vivo, or acts on DNA through its metabolites, and its non-glycoside homologue 4-demethylepipodophyllotoxin can inhibit microtubule assembly.

More

Etoposide is an effective component of lignans isolated from podophyllin. VP-16 is a cell cycle-specific anti-tumor drug that acts in the late S phase or G2 phase. Its action site is topoisomerase II, forming a stable cleavable complex between drug, enzyme and DNA, interfering with DNA topoisomerase II, making the damaged DNA unable to be repaired. By stabilizing the DNA breakage complex, it causes double-line breaks in DNA and topoisomerase II. It activates certain endonucleases in vivo, or acts on DNA through its metabolites, and its non-glycoside homologue 4-demethylepipodophyllotoxin can inhibit microtubule assembly.

33419-42-0 20
Atropine Sulfate Tablets
Main ingredient: Atropine. Chemical name: α-(Hydroxymethyl)phenylacetic acid 8-methyl-8-azabicyclo[3,2,1]-3-octyl ester sulfate monohydrate Molecular weight: (C17H23NO3)2·H2SO4·H2O
Name Description Content CAS NO. Registered Holders
Atropine

No specific pharmacological information is provided

More

No specific pharmacological information is provided

51-55-8 6
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