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Raloxifene hydrochloride 100 mg  | 99.56%

TargetMol

Raloxifene hydrochloride is a second generation selective estrogen receptor modulator (SERM) used to prevent osteoporosis in postmenopausal women. It has estrogen agonist effects on bone and cholesterol metabolism but behaves as a complete estrogen antagonist on mammary gland and uterine tissue.

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Raloxifene hydrochloride 50 mg  | 99.56%

TargetMol

Raloxifene hydrochloride is a second generation selective estrogen receptor modulator (SERM) used to prevent osteoporosis in postmenopausal women. It has estrogen agonist effects on bone and cholesterol metabolism but behaves as a complete estrogen antagonist on mammary gland and uterine tissue.

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Tigecycline 10 mg  | 99.94%

TargetMol

Tigecycline is a broad-spectrum glycylcycline antibiotic derived from tetracycline. Tigecycline binds to the 30S ribosomal subunit, thereby interfering with the binding of aminoacyl-tRNA to the mRNA-ribosome complex.

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Tigecycline 100 mg  | 99.94%

TargetMol

Tigecycline is a broad-spectrum glycylcycline antibiotic derived from tetracycline. Tigecycline binds to the 30S ribosomal subunit, thereby interfering with the binding of aminoacyl-tRNA to the mRNA-ribosome complex.

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Olanzapine 50 mg  | Purity Not Available

TargetMol

Olanzapine is an atypical antipsychotic that is used currently in the treatment of schizophrenia and bipolar illness.

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Olanzapine 500 mg  | Purity Not Available

TargetMol

Olanzapine is an atypical antipsychotic that is used currently in the treatment of schizophrenia and bipolar illness.

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Olanzapine 100 mg  | Purity Not Available

TargetMol

Olanzapine is an atypical antipsychotic that is used currently in the treatment of schizophrenia and bipolar illness.

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Alarelin Acetate 10 mg  | Purity Not Available

TargetMol

Alarelin Acetate is a synthetic GnRH agonist which can directly inhibit proliferation and DNA synthesis of rat GSMC through GnRH receptors.

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Alarelin Acetate 5 mg  | Purity Not Available

TargetMol

Alarelin Acetate is a synthetic GnRH agonist which can directly inhibit proliferation and DNA synthesis of rat GSMC through GnRH receptors.

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Dutasteride 10 mg  | Purity Not Available

TargetMol

Dutasteride is a 5-alpha-reductase inhibitor that inhibits both type-1 and type2 isoforms of the enzyme and is used to treat benign prostatic hyperplasia.

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