To enhance service speed and avoid tariff delays, we've opened a US warehouse. All US orders ship directly from our US facility.
| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC22782 | MDL-72527 Featured |
A polyamine oxidase (PAO) inhibitor that inhibits spermine oxidase and N1-acetylpolyamine oxidase with IC50 of 6.1 and 0.02 uM, respectively.
More description
|
|
| DC36493 | Dideoxyadenosine Featured |
Dideoxyadenosine is konwn as 2′,3′-Dideoxyadenosine (ddA), a specific adenylyl cyclase inhibitor, is useful in biological process and pathway studies involving adenylyl cyclase activity and cAMP pool modulation.
More description
|
|
| DC47250 | Nonanal |
Nonanal is a saturated fatty aldehyde with antidiarrhoeal activity.
More description
|
|
| DC47249 | Piperitone |
Piperitone is as a powerful repellent and antiappetent agent. Piperitone is very toxic to Cymbopogon schoenanthus (C. schoenanthus) adults, newly laid eggs and to neonate larvae. Insecticidal activity.
More description
|
|
| DC47247 | Tyrosylleucine TFA |
Tyrosylleucine (Tyr-Leu, YL) TFA, an orally active dipeptide, exhibits a potent antidepressant-like activity.
More description
|
|
| DC47243 | Dehydroglyasperin C |
Dehydroglyasperin C, a isoflavone, is a potent NAD(P)H:oxidoquinone reductase (NQO1) and phase 2 enzyme inducer. Dehydroglyasperin C has antioxidant, neuroprotective, cancer chemopreventive, and anti-inflammatory activities.
More description
|
|
| DC47227 | (−)-Myrtenal |
(−)-Myrtenal ((1R)-(−)-Myrtenal) is an orally active terpene with antitumour activity. (−)-Myrtenal ameliorates hyperglycemia by enhancing GLUT2 through Akt in the skeletal muscle and liver of diabetic rats.
More description
|
|
| DC47224 | GPX4-IN-3 |
GPX4-IN-3 (26a) is a potent glutathione peroxidase 4 (GPX4) inhibitor as a selective ferroptosis inducer. GPX4-IN-3 (26a) exhibits 71.7% inhibition for GPX4 with 1 μM.
More description
|
|
| DC47179 | Tyrosylleucine |
Tyrosylleucine (Tyr-Leu, YL), an orally active dipeptide, exhibits a potent antidepressant-like activity.
More description
|
|
| DC47178 | Mead acid |
Mead acid (5,8,11-Eicosatrienoic acid), an unsaturated (Omega-9) fatty acid, is an indicator of essential fatty acid deficiency.
More description
|
|
| DC47140 | Yadanzioside K |
Yadanzioside K is a natural quassinoid glucoside found in Brucea amarissima.
More description
|
|
| DC47105 | Complanatoside B |
Complanatoside B is a P. chinense Fisch flavonoid with potential anti-inflammatory effects.
More description
|
|
| DC47096 | Umckalin |
Umckalin is a oxygenated coumarin from Pelargonium sidoides.
More description
|
|
| DC47086 | 7,3′,4′-Tri-O-methyleriodictyol |
7,3′,4′-Tri-O-methyleriodictyol is a flavonoid with an antimutagenic activity. 7,3′,4′-Tri-O-methyleriodictyol inhibits the furylfuramide-induced SOS response and has potency as bioantimutagens.
More description
|
|
| DC47075 | Syringetin |
Syringetin, a flavonoid derivative, is associated with increased BMP-2 production. Syringetin stimulates osteoblast differentiation at various stages, from maturation to terminally differentiated osteoblasts.
More description
|
|
| DC47065 | Idetrexed |
Idetrexed is a thymidylate synthase inhibitor specifically transported into alpha-folate receptor (alpha-FR)-overexpressing tumors. BGC 945 inhibited thymidylate synthase with a Ki of 1.2 nmol/L.
More description
|
|
| DC47064 | Hexasodium phytate |
Hexasodium phytate (Phytic acid hexasodium) is a phosphorus storage compound of seeds and cereal grains. Hexasodium phytate has a strong ability to chelate multivalent metal ions, specially zinc, calcium, iron and as with protein residue. Hexasodium phytate inhibits the enzymatic superoxide source xanthine oxidase (XO), and has antioxidative, neuroprotective, anti-inflammatory effects.
More description
|
|
| DC47047 | Polθ-IN-1-d3 |
Polθ-IN-1-d3 (example 1) is a deuterated Polθ inhibitor used for cancer study (extracted from patent WO2021028670).
More description
|
|
| DC47026 | 4-Phenyl-7,8-dihydroxycoumarin |
4-Phenyl-7,8-dihydroxycoumarin is a coumarin derivative and can be used for bronchiectasiss research.
More description
|
|
| DC47022 | Quercetin 3,3'-dimethyl ether |
Quercetin 3,3'-dimethyl ether possesses antioxidant acticity.
More description
|
|
| DC47020 | Sophoramine |
Sophoramine ((-)-Sophoramine), an alkaloid, is a dehydro-derivative of Matrine.
More description
|
|
| DC47016 | Yadanzioside M |
Yadanzioside M is a natural compound with anti-cancer activity.
More description
|
|
| DC47015 | D-(+)-Fucose |
D-(+)-Fucose is a nonmetabolizable analogue of l-arabinose. D-(+)-Fucose prevents growth of Escherichia coli B/r on a mineral salts medium plus l-arabinose by inhibiting induction of the l-arabinose operon. D-fucose is a potent inducer of beta-methylgalactoside permease (MGP).
More description
|
|
| DC47010 | Astragenol |
Astragenol is an intermediate used for Astragenol derivative synthesis. Astragenol derivatives are promising anti-inflammatory agents for prostate cancer research.
More description
|
|
| DC46995 | Kisspeptin-10, rat TFA |
Kisspeptin-10, rat TFA is a potent vasoconstrictor and inhibitor of angiogenesis. Kisspeptin-10, rat TFA is a ligand for the rodent kisspeptin receptor (KISS1, GPR54). Kisspeptin-10 TFA reduces Methotrexate-induced reproductive toxicity as a potential antioxidant compound.
More description
|
|
| DC46994 | Uty HY Peptide (246-254) (TFA) |
Uty HY Peptide (246-254) TFA, derived from the ubiquitously transcribed tetratricopeptide repeat gene on the Y chromosome (UTY) protein as an H-Y epitope, H-YDb, is a male-specific transplantation antigen H-Y.
More description
|
|
| DC46992 | Simethicone |
Simethicone (Simeticone) is a nonabsorbable, surface-active, antifoaming agent.
More description
|
|
| DC46991 | PKG inhibitor peptide |
PKG inhibitor peptide is an ATP-competitive inhibitor of cGMP-dependent protein kinase (PKG), with a Ki of 86 μM.
More description
|
|
| DC46990 | JAG-1, scrambled TFA |
JAG-1, scrambled (scJag-1) TFA is a scrambled sequence of JAG-1 (Jagged-1 protein). JAG-1, scrambled TFA has a random sequence of the amino acids that are the same as the active fragment. JAG-1, scrambled TFA is usually used as a negative control.
More description
|
|
| DC22156 | ML-191 Featured |
ML-191 is a potent, selective GPR55 antagonist with 160 nM potency for GPR55 and >100-fold selectivity against GPR35, CB1 and CB2.
More description
|
|