| Cat.No. | Name | Information |
|---|---|---|
| M38764 | Indinavir | Indinavir (MK-639 free base) is an orally active and selective HIV-1 protease inhibitor with a Ki of 0.54 nM for PR. Indinavir exhibits anticancer activity by inhibiting the activation of MMPs-2 hydrolysis, anti-angiogenesis and inducing apoptosis. Indinavir is also a SARS-CoV 3CLpro inhibitor. |
| M38760 | Glycoborinine | Glycoborinine, a natural carbazole alkaloid, can be isolated from Glycosmis pentaphylla. Glycoborinine induces HepG2 cell apoptosis through mitochondrial pathway. Glycoborinine also inhibits HIV replication in cells. |
| M38750 | γ-Fagarine | γ-Fagarine is a furoquinoline alkaloid naturally occurring in Rutae Herba. γ-Fagarine has strong anti-HCV activities with IC50 of 20.4 μg/mL and is also a sister chromatid exchanges (SCEs) inducer. |
| M38728 | (±)-Pinoresinol | (±)-Pinoresinol is a potent antifungal agent. (±)-Pinoresinol shows antifungal activity. |
| M38723 | Demethoxyencecalin | Demethoxyencecalin is a chromene isolated from Helianthus annuus, has antifungal activities. |
| M38718 | Methyl p-coumarate | Methyl p-coumarate (Methyl 4-hydroxycinnamate), an esterified derivative of p-Coumaric acid (pCA), is isolated from the flower of Trixis michuacana var longifolia. Methyl p-coumarate could inhibit the melanin formation in B16 mouse melanoma cells. |
| M38717 | Thiophanate-Methyl | Thiophanate-Methyl is a systematic fungicide. |
| M38715 | Luteolin-7-rutinoside | Luteolin-7-rutinoside has both anti-arthritic and antifungal activities, can result in a combination therapy for the treatment of fungal arthritis due to C. albicans infection. |
| M38703 | Chalcone | Chalcone is isolated from Glycyrrhiza uralensis and used to synthesize chalcone derivatives. Chalcone derivatives possess varied biological and pharmacological activity, including anti-inflammatory, antioxidative, antibacterial, anticancer, and anti-parasitic activities. |
| M38700 | Horminone | Horminone is an abietan diterpene quinone that can be isolated from Labiatae family. Horminone increases of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) serum levels in vivo. Horminone inhibits the growth of Trypanosoma cruzi and shows antibacterial activity. |
| M38694 | Cefuroxime | Cefuroxime is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime has a broad spectrum activity against Gram-positive and Gram-negative bacteria. |
| M38683 | Muramic acid | Muramic acid is a component in many Gram-positive bacterial cell walls, as marker for Gram-positive bacteria. |
| M38682 | Glyasperin D | Glyasperin D is a flavonoid isolated from Glycyrrhiza uralensis, and possesses weaker anti-Helicobacter pylori activity. |
| M38679 | Aflatoxin M1 | Aflatoxin M1 is a major metabolite of Aflatoxin B1. Aflatoxin M1 is a mycotoxin produced by the fungi Aspergillus flavus and Aspergillus parasiticus. The level of toxicity associated with Aflatoxin is Aflatoxin B1>Aflatoxin M1>Aflatoxin G1>Aflatoxin B2>Aflatoxin M2>Aflatoxin G2. |
| M38676 | Senecivernine | Senecivernine, a pyrrolizidine alkaloid isolated from Senecio species, exhibits a weakly mutagenic activity. |
| M38664 | Chromomycin A3 | Chromomycin A3 is an aureolic acid-type antitumor antibiotic. Chromomycin A3 forms dimeric complexes with divalent cations, such as Mg2+, which strongly binds to the GC rich sequence of DNA to inhibit DNA replication and transcription. |
| M38658 | Macranthoside B | Macranthoside B, isolated from Flos Lonicerae, possesses anti-bacterial activity. |
| M38655 | N-Acetyltyramine | N-Acetyltyramine is a quorum-sensing inhibitor (QSI) compound produced by V. alginolyticus M3-10. N-Acetyltyramine is capable of inhibiting the QS of C. violaceum ATCC 12472. N-acetyltyramine reverses resistance in Doxorubicin-resistant leukemia P388 cells. |
| M38631 | Imipenem | Imipenem (MK0787) is an antibiotic and has the excellent activity against a broad range of gram-positive and gram-negative aerobic and anaerobic bacteria. Imipenem can be used for the research of carbapenem-nonsusceptible and P. aeruginosa biofilm infections. |
| M38627 | Anhydrotetracycline | Anhydrotetracycline shows dose-dependent and potent inhibition of tetracycline destructases in vitro. |
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