YN251436 Chlorogenic acid 327-97-9

Chlorogenic acid is a hydroxycinnamic acid and a member of a family of naturally occurring organic compounds.

YN480344 Nicarbazin 330-95-0

Nicarbazin, an effective anticoccidial, is also a wide-spectrum anti-parasitic drug.

YN251220 Diazinon 333-41-5

Diazinon is a thiophosphoric acid ester, is a nonsystemic organophosphate insecticide, used to control cockroaches, silverfish, ants, and fleas.

YN371224 HQNO 341-88-8

HQNO is a natural quinolone secreted by P. aeruginosa. HQNO is a potent inhibitor of the electron transport chain with Kd of 64 nM for the ubiquinol-ferricytochrome c oxidoreductase segment (Complex III) of the ...

YN251323 Dicloxacillin sodium 343-55-5

Dicloxacillin is a β-lactamase resistant penicillin similar to oxacillin and it has activity against gram-positive/negative aerobic and anaerobic bacteria.

YN251229 Sulbentine 350-12-9

Sulbentine (Dibenzthione) is an azoleantifungal agentthat has fungistatic and fungicidal activities. Sulbentine is used as a locally acting antimycoticin vivo.

YN251030 Nalidixic acid 389-08-2

Nalidixic acid is a synthetic 1,8-naphthyridine antimicrobial agent with a limited bacteriocidal spectrum. It is an inhibitor of the A subunit of bacterial DNA gyrase.

YN440427 Fangchinoline 436-77-1

Fangchinoline is a phytochemical that has been shown to elicit anti-cancer effects in prostate and breast cancer cell lines via inducing G1 cell cycle arrest. It has also been shown to possess neuroprotective activity.

YN250996 Metronidazole 443-48-1

Metronidazole, a synthetic antibacterial and antiprotozoal agent of the nitroimidazole class, is used against protozoa.

YN251332 Ethoxzolamide 452-35-7

Ethoxzolamide is an inhibitor of the metalloenzyme carbonic anhydrase, which inhibits hCA I, hCA II, hCA IV, hCA VI and hCA VII with K_i of 25 nM, 8 nM, 93 nM, 43 nM and 0.8 nM, respectivel...

YN373341 Coniferyl alcohol 458-35-5

Coniferyl alcohol is an intermediate in biosynthesis of eugenol and of stilbenoids and coumarin. Coniferyl alcohol specifically inhibits fungal growth.

YN250135 Mitoguazone 459-86-9

Mitoguazone (Methylglyoxal-bis(guanylhydrazone)) is a synthetic polycarbonyl derivative with potent antineoplastic activity. Mitoguazone is a brain-penetrant and competitiveS-adenosyl-methionine decarboxylase (SAMDC)inhibitor tha...

YN250236 Haemanthamine 466-75-1

Haemanthamine is a crinine-type alkaloid isolated from theAmaryllidaceaeplants with potent anticancer activity. Haemanthamine targets ribosomal that inhibits protein biosynthesis during the elongation stage of translation. Haemanthamine...

YN482665 Hecogenin 467-55-0

Hecogenin is a steroid saponin isolated fromAgave sisalana and is a selective inhibitor ofhuman UDP-glucuronosyltransferases. Hecogenin has a wide spectrum of pharmacological activities, including anti-inflammatory, antifungal and ...

YN251647 Hamamelitannin 469-32-9

Hamamelitannin, a polyphenol extracted from the bark ofHamamelis virginiana, is aquorum-sensing (QS)inhibitor. Hamamelitannin increases antibiotic susceptibility ofstaphylococcus aureusbiofilms by affecting peptidoglycan biosynthesis ...

YN481190 (-)-Cedrene 469-61-4

(-)-Cedrene (α-cedrene) is a sesquiterpene constituent of cedarwood oils, with anti-leukemic, antimicrobial and anti-obesity activities.

YN373303 1-Kestose 470-69-9

1-Kestose, the smallest fructooligosaccharide component, which efficiently stimulatesFaecalibacterium prausnitziias well as Bifidobacteria.

YN251738 Zerumbone 471-05-6

Zerumbone is a monocyclic sesquiterpene compound isolated from the rhizomes ofZingiber zerumbetSmith. Zerumbone potently inhibits the activation ofEpstein-Barr viruswith an IC50 of 0.14 mM. Zerumbone has anti-cancer, antioxidant, ...

YN250474 Neoabietic acid 471-77-2

Neoabietic acid is an abietic-type acid isolated from the oleoresin and rosin ofPinus palustris. Neoabietic acid is highly susceptible to mineral acid. Neoabietic acid has antibacterial activity in vitro .

YN370316 Betulinic acid 472-15-1

Betulinic acid, a pentacyclic triterpenoid from Syzigium claviflorum, is a inhibitor of HIV-1 with EC50 of 1.4 &mu M. Phase 1/2.