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20

Compounds

Cat No. Product Name Synonyms Targets
TQ0089 Juglanin Apoptosis , JNK , Autophagy
Juglanin is a JNK activator. Juglanin with inflammation and anti-tumor activities. It can induce apoptosis and autophagy on human breast cancer cells.
T5669 Citric acid monohydrate Others
Citric Acid Monohydrate is a tricarboxylic acid found in citrus fruits. Citric acid is used as an excipient in pharmaceutical preparations due to its antioxidant properties. It maintains stability of active ingredients a...
T5S0636 Citric acid Citro,Citretten Apoptosis , Others , Endogenous Metabolite , Antibacterial , Antibiotic
1. Citric acid (Citro) (1-2 g/kg) can decrease brain lipid peroxidation and inflammation, liver damage, and DNA fragmentation. 2. Citric acid denture cleansers can reduce C. albicans biofilm accumulation and cell viabili...
T7969 Dipyrithione Others
Dipyrithione appears to have novel cytotoxicity and potent broad-spectrum antitumor activity
T22260 Aminopurvalanol A CDK
Aminopurvalanol A is a competitive, selective and cell-permeable inhibitor of cyclin-dependent kinase (CDK) that potently inhibits Cyclin A/cdk2, Cyclin B/cdk1, Cyclin E/cdk2, and P35/cdk5 with IC50 of 33 nM, 33 nM, 28 n...
T9244 σ1 Receptor antagonist-1 Sigma receptor
σ1 Receptor antagonist-1 is a selective sigma 1 receptor antagonist.
T7057 Methylstat Histone Demethylase , Others
Methylstat is a methyl ester prodrug of a Jumonji C domain-containing histone demethylase (JMJD) inhibitor that has favorable cell permeability. The free acid of methylstat inhibits JMJD2A, JMJD2C, JMJD2E, PHF8, and JMJD...
T1753 D-64131 Microtubule Associated
D-64131 is a tubulin polymerization inhibitor with an IC50 value of 0.53 μM.
T19664 ON1231320 GBO-006 Apoptosis , PLK
ON1231320 (GBO-006) is a Polo-like kinase 2 (PLK2) inhibitor.
T6308 Stattic STAT3 Inhibitor V Apoptosis , STAT
Stattic (STAT3 Inhibitor V) is a STAT3 inhibitor (IC50=5.1 μM) that selectively inhibits STAT3 activation, dimerization, and nuclear translocation. Stattic has antitumor activity and induces apoptosis.
T8800 NSAH 2-hydroxy-N'-[(E)-(2-hydroxynaphthalen-1-yl)methylidene]benzohydrazide DNA/RNA Synthesis
NSAH (2-hydroxy-N'-[(E)-(2-hydroxynaphthalen-1-yl)methylidene]benzohydrazide) is a nonnucleoside inhibitor of human ribonucleotide reductase (hRR).with cell-free IC50 of 32 μM and cell-based IC50 of ~250 nM, respectively...
T8616 Fasentin N-[4-chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide transporter
Fasentin (N-[4-chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide) is an inhibitor of GluT1.
T8742 G5-7 JAK2 inhibitor G5-7 Apoptosis , JAK
JAK2 inhibitor G5-7 (JAK2 inhibitor G5-7) is an orally active JAK2 inhibitor, selectively inhibits JAK2–mediated phosphorylation and activation of EGFR (Tyr1068) and STAT3 by binding to JAK2. G5-7 has the potential for g...
T3S1416 Decursin Decursinol angelate,(+)-Decursin Apoptosis , PKC
1. Decursin (Decursinol angelate) is able to attenuate kainic acid-induced seizures and could have potential as an antiepileptic drug. 2. Decursin exhibits hepatoprotective effects , potentially by inhibiting the TGF-β1 ...
T16813 RX-3117 fluorocyclopentenylcytosine,TV-1360 Nucleoside Antimetabolite/Analog
RX-3117 (fluorocyclopentenylcytosine) is a novel a cytidine analog. RX-3117 displays anticancer activity in several cancer cell lines, including gemcitabine-resistant variants.
T1882 Meisoindigo N-Methylisoindigotin,Methylisoindigotin,Natura-α,Dian III Apoptosis
Meisoindigo (Natura-α) is a derivative of indigo natural, might induces apoptosis and myeloid differentiation of acute myeloid leukemia (AML).
T3459 VK3-OCH3 2-[(2-Methoxy)ethylthio]-3-methyl-1,4-na Others
VK3-OCH3 (2-[(2-Methoxy)ethylthio]-3-methyl-1,4-na) is a selective antitumor agent via heme oxygenase (HO-1) related mechanisms; Vitamine K3 analogue.
T9003 CVT-11127 Dehydrogenase
CVT-11127 is an StearoylCoA Desaturase-1 (SCD1) inhibitor.
T5777 Phaseoloidin Others
Phaseoloidin, a homogentisic acid glucoside from Nicotiana attenuata trichomes, contributes to the plant's resistance against lepidopteran herbivores.
TN4760 Phaseollidin hydrate Antifection
Phaseollidin hydrate shows less antifungal activity than the original phytoalexin phaseollidin.
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TargetMol