BOC Sciences

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BOC Sciences provides a wide variety of custom services which range from bulk compounds to specialty species in the pharmaceutical, agrochemical, and biotechnology industries. We are committed to providing our customers with the best products and services at the most competitive prices. Given diverse packing options for most of our chemicals, you are welcome to order the desired compounds in any quantities from a few mg to several kg along with all the relevant technical reports. We sincerely hope that our unremitting pursuits of excellence, success, and professionalism will add immense value to your research and development projects!

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(-)-(1R,3S)-3-Aminocyclopentanecarboxylic acid inquire  | Purity Not Available

BOC Sciences

(-)-(1R,3S)-3-Aminocyclopentanecarboxylic acid is used in the synthesis of aminocyclopentanecarboxylic acid-containing cyclic RGD peptides. It is also used to prepare BMS-457, a potent and selective CCR1 antagonist.

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(-)-2-(2-Hydroxyethyl)clavam inquire  | Purity Not Available

BOC Sciences

(-)-2-(2-Hydroxyethyl)clavam is an oxypenicillane antibiotic produced by Streptomyces antibiotcus var. antibioticus Tu 1718. It has anti-fungal and weak anti-Gram-positive and negative bacteria activity.

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(-)-Blebbistatin inquire  | Purity Not Available

BOC Sciences

(-)-Blebbistatin is a cell-permeable inhibitor for non muscle myosin II ATPase with IC50 of ~2 μM, does not inhibit myosin light chain kinase, inhibits contraction of the cleavage furrow without disrupting mitosis or contractile ring assembly.

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(-)-Carbovir inquire  | Purity Not Available

BOC Sciences

(-)-Carbovir, is a nucleoside/nucleotide reverse transcriptase inhibitor (NRTI) caused mitochondrial toxicity in human hepatoma carcinoma cell.

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(-)-Catechin gallate 25 mg  | ≥0.98%

BOC Sciences

(-)-Catechin gallate, a minor polyphenolic constituent in green tea, is used to study its cytotoxicity. It enhances Fe(2+)-induced, lipid peroxidation. It also inhibits aromatase activity, an enzyme that converts androgens to estrogen and is thought to play a role in the etiology of breast cancer.

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(-)-Epicatechin gallate inquire  | Purity Not Available

BOC Sciences

(−)-Epicatechin gallate (ECG) is a natural catechin with a single galloyl group. Like EGCG, it inhibits the growth of cancer cells and has anti-inflammatory effects. The hydroxyl groups of ECG contribute to its potent antioxidant activity and facilitate the killing of methicillin-resistant strains of S. aureus. (-)-Epicatechin gallate is a natural compound found in the […]

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(-)-Epigallocatechin inquire  | Purity Not Available

BOC Sciences

(-)-Epigallocatechin (EGC) is a natural flavonoid isolated from herbs of Berchemia kulingensis Schneid, and it has prominent antiplatelet activity and blood anticoagulation in a dose-dependent manner. (-)-Epigallocatechin is a natural compound, it can also be used in cosmetics material.

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(-)-Epigallocatechin gallate inquire  | Purity Not Available

BOC Sciences

EGCG is an antioxidant extracted from green tea, reduces Aβ42-induced cell death in three different cell types and inhibits β-secretase (IC50 = 1.6 μM). (-)-Epigallocatechin gallate is a natural compound found in the woods of Acacia catechu (L.F.) Willd. It can be used in cosmetic material.

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(-)-Epigallocatechin gallate inquire  | Purity Not Available

BOC Sciences

EGCG is an antioxidant extracted from green tea, reduces Aβ42-induced cell death in three different cell types and inhibits β-secretase (IC50 = 1.6 μM). (-)-Epigallocatechin gallate is a natural compound found in the woods of Acacia catechu (L.F.) Willd. It can be used in cosmetic material.

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(-)-Harveynone inquire  | Purity Not Available

BOC Sciences

It is produced by the strain of Curvularia harveyi. It can inhibit the formation of Sea urchin eggs Spindle.

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(-)-Huperzine A (HupA) inquire  | Purity Not Available

BOC Sciences

(-)-Huperzine A is a potent, highly specific and reversible inhibitor of acetylcholinesterase (AChE) with Ki of 7 nM, exhibiting 200-fold more selectivity for G4 AChE over G1 AChE. Also acts as an NMDA receptor antagonist. Phase 4.

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(-)-Neplanocin A inquire  | Purity Not Available

BOC Sciences

(−)-Neplanocin A potently and irreversibly inactivates SAH hydrolase (Ki = 8.39 nM). It has antitumor activity against mouse leukemia L1210 cells and broad-spectrum antiviral activity. Neplanocin A is more potent against vesicular stomatitis than the reversible SAH hydrolase inhibitor 3-deazaneplanocin (ID50 = 0.07 and 0.3 μg/ml, respectively).

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