DC37279Cetylpyridinium chloride
Cetylpyridinium chloride is a Germicide, Bactericide, and Disinfectant.
View activity & pricesDC Chemicals · Research reagentsDC37279 
DCAPI1566
DC8944
DC9009
DC67959
DCC5248
DC78346
DC8629
DC67193
DC65707
DC67195
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DC48542
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DCAPI1045
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Small Molecule Research Tools
2816 products · Page 52 of 59
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DC37279DCAPI1566Cytarabine hydrochloride
For the detailed information of Cytarabine hydrochloride, the solubility of Cytarabine hydrochloride in water, the solubility of Cytarabine hydrochloride in DMSO, the solubility of Cytarabine hydrochloride in PBS…
View activity & pricesDC89445-Fluorouracil
5-Fluorouracil is a potent antitumor agent that affects pyrimidine synthesis by inhibiting thymidylate synthetase thus depleting intracellular dTTP pools.5-Fluorouracil is metabolized to ribonucleotides and…
View activity & pricesDC9009Thalidomide
Thalidomide can directly inhibit angiogenesis induced by bFGF or VEGF in vivo.Thalidomide was commonly used therapeutically in the late 1950's; however, it was withdrawn from the market when it was discovered to cause…
View activity & pricesDC67959Tex Red-X Acid
Tex Red-X dye is an innovative alternative to Tex Red. A key difference lies in its chemical structure - it features an additional seven - atom aminocaproyl spacer ("X") between the fluorophore and the carboxyl group.…
View activity & pricesDCC5248Trpm2 Inhibitor A23
Novel selective inhibitor of the transient receptor potential melastatin 2 (TRPM2) channel, exhibiting TRPM2 selectivity over TRPM8 and TRPV1 channels as well as phospholipase A2 and showing neuroprotective activity in…
View activity & pricesDC78346AH001
AH001 is a orally active RhoA inhibitor, which binds a cryptic pocket proximate to GDP within RhoA with a KD of 73.16 nM. AH001 interacts with GDP, stabilizing RhoA’s interaction with its endogenous inhibitor, RhoGDIα.…
View activity & pricesDC8629Trilostane(Win 24540; Modrastane)
Trilostane(Win 24540; Modrastane) is an inhibitor of 3 β-hydroxysteroid dehydrogenase used in the treatment of Cushing's syndrome.Trilostane is an inhibitor of 3 β-hydroxysteroid dehydrogenase (3-β-HSD or delta 5-delta…
View activity & pricesDC67193N-(3S)-3-Piperidinyl-2-thiophenesulfonamide
N-(3S)-3-Piperidinyl-2-thiophenesulfonamide is available from DC Chemicals for laboratory research. Contact us for application-specific product information.
View activity & pricesDC65707Thiophene, 2-methyl-5-(phenylsulfonyl)-
Thiophene, 2-methyl-5-(phenylsulfonyl)- is available from DC Chemicals for laboratory research. Contact us for application-specific product information.
View activity & pricesDC67195N-(2-aminoethyl)-5-chlorothiophene-2-sulfonamide
N-(2-aminoethyl)-5-chlorothiophene-2-sulfonamide is available from DC Chemicals for laboratory research. Contact us for application-specific product information.
View activity & pricesDC657083-Methyl-5-(methylsulfamoyl)thiophene-2-carboxylic acid
3-Methyl-5-(methylsulfamoyl)thiophene-2-carboxylic acid is available from DC Chemicals for laboratory research. Contact us for application-specific product information.
View activity & pricesDC67194(5-pyrrolidin-1-ylsulfonyl-2-furyl)methanamine
(5-pyrrolidin-1-ylsulfonyl-2-furyl)methanamine is available from DC Chemicals for laboratory research. Contact us for application-specific product information.
View activity & pricesDC67196phenyl 2,5-Dichloro-3-Thienyl Sulfone
phenyl 2,5-Dichloro-3-Thienyl Sulfone is available from DC Chemicals for laboratory research. Contact us for application-specific product information.
View activity & pricesDC74017HTL0041178
HTL0041178 is a potent GPR52 agonist with EC50 of 27.5 nM (human or rat GPR52).
View activity & pricesDC60707YTHDC1 inhibitor 40 (compound 40)
YTHDC1 inhibitor 40 is a potent, selective m6A reader YTHDC1 inhibitor with ITC Kd of 49 nM, HTRF IC50 of 0.35 uM. Compound 40 shows antiproliferative activity against the acute myeloid leukemia (AML) cell lines THP-1,…
View activity & pricesDC10733Sutezolid (PNU-100480)
Sutezolid (PNU-100480) is an oxazolidinone antimicrobial being developed for the treatment of tuberculosis.Target: AntibacterialSutezolid is a much-awaited drug candidate for treatment of Mycobacterium tuberculosis.…
View activity & pricesDC71665Val-Cit-PAB-MMAF
Val-Cit-PAB-MMAF is a drug-linker conjugate for ADC. Val-Cit-PAB-MMAF contains the ADCs linker (peptide Val-Cit-PAB) and a potent tubulin polymerization inhibitor MMAF.
View activity & pricesDC34489DOCK5-IN-C21
DOCK5-IN-C21 functions as an allosteric inhibitor targeting the guanine nucleotide exchange factor DOCK5, effectively modulating its activity through a non-competitive mechanism.
View activity & pricesDC74445FL-1607
FL-1607, a novel Fam20C inhibitor, has shown remarkable anti-proliferative effects in triple-negative breast cancer (TNBC) cells. This compound induces apoptosis and significantly reduces the migration ability of…
View activity & pricesDC8914Indacaterol
Indacaterol is a potent, orally administered ultra-long-acting β2 adrenergic receptor (ADRB2) agonist, widely recognized for its therapeutic potential in respiratory and cardiovascular conditions. By selectively…
View activity & pricesDC31184Idoxuridine
Idoxuridine is an anti-herpesvirus antiviral and anticancer drug. It is a nucleoside analogue, a modified form of deoxyuridine, similar enough to be incorporated into viral DNA replication, but the iodine atom added to…
View activity & pricesDC33159PF-06279794
PF-06279794, also known as PF-794, is a potent, selective and ATP-competitive TNIK inhibitor.
View activity & pricesDC8385Disodium (R)-2-Hydroxyglutarate
D-alpha-Hydroxyglutaric acid disodium salt is a weak competitive α-Ketoglutarate(α-KG)-dependent dioxygenase inhibitor with Ki of 10.87±1.85 mM. Ki for L-Hydroxyglutaric acid (L-2-HG) is 0.628±0.036 mM.
View activity & pricesDC67510Fluorocholine chloride
Fluorocholine chloride serves as a versatile biochemical tool for life science investigations, functioning both as an organic compound and biological marker in various research applications.
View activity & pricesDC22902SNC-80
SNC80 (NIH 10815) is a potent, highly selective and non-peptide δ-opioid receptor agonist with a Ki of 1.78 nM and an IC50 of 2.73 nM. SNC80 also selectively activates μ-δ heteromer in HEK293 cells with an EC50 of 52.8…
View activity & pricesDC67437PI-2620 precursor
PI-2620 precursor is the precursor of PI2620. 18F-PI-2620 is a PET tracer with high binding affinity for aggregated tau, a key pathologic feature of Alzheimer disease (AD) and other neurodegenerative disorders.
View activity & pricesDCY-118Lycorine hydrochloride
For the detailed information of Lycorine hydrochloride, the solubility of Lycorine hydrochloride in water, the solubility of Lycorine hydrochloride in DMSO, the solubility of Lycorine hydrochloride in PBS buffer, the…
View activity & pricesDC26061Questiomycin A
Questiomycin A is a phenoxazine and a chromophore that has been found in Streptomyces and has antibacterial and anticancer activities.
View activity & pricesDC9637Desmopressin (Acetate)
Desmopressin(DDAVP) acetate is the synthetic analogue of the antidiuretic hormone arginine vasopressin. IC50 Value:Target: Vasopressin ReceptorThe antidiuretic properties of desmopressin have led to its use in polyuric…
View activity & pricesDC48542LM10
LM10 is a potent inhibitor of tryptophan 2,3-dioxygenase (TDO). Tryptophan 2,3-dioxygenase (TDO) is an unrelated hepatic enzyme that also degrades tryptophan along the kynurenine pathway. LM10 has the potential for the…
View activity & pricesDC74584LY2880070
LY2880070 is an orally active inhibitor of CHK1. LY2880070 can be used as an anticancer agent and shows promise in preclinical models of pancreatic ductal adenocarcinoma (PDAC) when used in combination with…
View activity & pricesDC68137PAA-38 HCl
PAA-38 is a highly potent selective inhibitor targeting bacterial prolyl-tRNA synthetase (ProRS). PAA-38 againsts Pseudomonas aeruginosa ProRS (PaProRS) with a Kd value of 0.399 nM and an IC50 value of 4.97 nM. PAA-38…
View activity & pricesDC67516Peptide T7 with N-Cysteine
This study developed CRD-PEG-T7, a prostate cancer-targeting gene delivery system featuring a disulfide-crosslinked arginine-aspartic acid peptide vector modified with T7 targeting ligands for selective pDNA delivery…
View activity & pricesDCAPI1045Hydroxyurea (Cytodrox)
For the detailed information of Hydroxyurea (Cytodrox), the solubility of Hydroxyurea (Cytodrox) in water, the solubility of Hydroxyurea (Cytodrox) in DMSO, the solubility of Hydroxyurea (Cytodrox) in PBS buffer, the…
View activity & pricesDC10423Motixafortide(BKT140)
BKT140 4-fluorobenzoyl is a novel CXCR4 antagonist with an IC50 vakue of ～1 nM. Sequence: 4F-Benzoyl-Arg-Arg-{2-Naph-Ala}-Cys-Tyr-{Cit}-Lys-Lys-Pro-Tyr-Arg-{Cit}-Cys-Arg-NH2(Disulfide bridge: Cys4-Cys13).
View activity & pricesDC31256Mifepristone (RU486)
Mifepristone (RU-486) is a potent steroidal antagonist exhibiting subnanomolar affinity for progesterone receptors (PR IC₅₀ = 0.2 nM) and nanomolar activity against glucocorticoid receptors (GR IC₅₀ = 2.6 nM). This…
View activity & pricesDC72952Savirin
Savirin (S. aureus virulence inhibitor) is a small molecule that targets the agr (accessory gene regulator) quorum sensing system in Staphylococcus aureus (S. aureus). The agr system is a key regulatory pathway that…
View activity & pricesDC23893Foxy-5(Wnt5a peptide mimetic)
Foxy-5 is a mimicking peptide of WNT5A which is a non-canonical member of the Wnt family. Foxy-5 is a WNT5A agonist and effectively reduces the metastatic spread of WNT5A-low prostate cancer cells in an orthotopic…
View activity & pricesDC22504Leuprorelin
Leuprolide is an agonist at pituitary GnRH receptors. Target: GnRH receptorLeuprorelin is a gonadotrophin-releasing hormone (GnRH) analogue used to treat a wide range of sex hormone-related disorders including advanced…
View activity & pricesDC71255MOTS-c
MOTS-c, a mitochondria-derived peptide (MDP), exerts antinociceptive and anti-inflammatory effects through activating AMPK pathway and inhibiting MAP kinases-c-fos signaling pathway.
View activity & pricesDC65640Selank
TP-7 (Selanc) is a heptapeptide with anxiolythic properties.
View activity & pricesDC26045Semax
Semax is a synthetic peptide analog of adrenocorticotropic hormone (ACTH) (4-10) that has neuroprotective, analgesic, and anxiolytic properties.In vivo, semax (0.3 mg/kg) reduces cortical nitric oxide (NO) production…
View activity & pricesDCH-009Quercetin
For the detailed information of Quercetin, the solubility of Quercetin in water, the solubility of Quercetin in DMSO, the solubility of Quercetin in PBS buffer, the animal experiment（test） (test) of Quercetin, the cell…
View activity & pricesDC24126Triptorelin
Triptorelin is a GnRH agaonist shown to inhibit estradiol-induced cancer cell proliferation
View activity & pricesDC70577LY3502970 (Orforglipron)
LY-3502970 (Orforglipron) is a potent, selective, orally active non-peptide agonist of glucagon-like peptide-1 (GLP-1) receptor.LY3502970 is a partial agonist, biased toward G protein activation over β-arrestin…
View activity & pricesDC22621Elacridar hydrochloride
Elacridar Hcl (GF120918; GW0918) is a P-glycoprotein inhibitor, and has been used both in vitro and in vivo as a tool inhibitor of P-glycoprotein (Pgp) to investigate the role of transporters in the disposition of…
View activity & pricesDC1011Lorcaserin
LLorcaserin (APD-356)is a weight-loss drug developed by Arena Pharmaceuticals. It has serotonergic properties and acts as an anorectic
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