231 Results for "

Woodwardia orientalis Sw.

" in MedChemExpress (MCE) Product Catalog:
Products (231)

231 Results for "Woodwardia orientalis Sw." in MCE Product Catalog:

30
30 Publications Verification
Cat. No.: HY-P80137
Synonyms: GAPDH; GAPD; CDABP0047; OK/SW-cl.12; Glyceraldehyde-3-phosphate dehydrogenase; Peptidyl-cysteine S-nitrosylase GAPDH

Host:  

Rabbit

Application:  

WB, ICC/IF, IHC-P, FC, IP

Reactivity:  

Human, Mouse, Rat, Chicken

10
10 Cited Publications
Cat. No.: HY-109049
CAS No.: 1467093-03-3
Purity:  98.85%
Synonyms: SM04690; Lorecivivint
Target:  

Wnt

Research Areas:  

Inflammation/Immunology Cancer

Adavivint (SM04690; Lorecivivint) is a potent and selective inhibitor of canonical Wnt signaling, with an EC50 of 19.5 nM via a high-throughput TCF/LEF-reporter assay in SW480 colon cancer cells .
9
9 Cited Publications
Cat. No.: HY-P80670
Synonyms: FTH1; FTH; FTHL6; OK/SW-cl.84; PIG15; Ferritin heavy chain; Ferritin H subunit; Cell proliferation-inducing gene 15 protein

Host:  

Rabbit

Application:  

WB, ICC/IF

Reactivity:  

Human, Mouse, Rat, Hamster

7
7 Cited Publications
Cat. No.: HY-16968
CAS No.: 459147-39-8
Target:  

15-PGDH

Research Areas:  

Others

SW033291 is a potent and high-affinity inhibitor of 15-PGDH with a Ki of 0.1 nM. SW033291 increases prostaglandin PGE2 levels in bone marrow and other tissues. SW033291 also promotes tissue regeneration .
7
7 Cited Publications
Cat. No.: HY-12032
CAS No.: 328543-09-5
Purity:  99.44%
Target:  

PARP

Research Areas:  

Cancer

AG14361 is a potent PARP-1 inhibitor, with a Ki of < 5 nM, and in permeabilized SW620 and intact SW620 cells, the IC50s are 29 nM and 14 nM, respectively.
5
5 Cited Publications
Cat. No.: HY-115475
CAS No.: 2126744-35-0
Purity:  99.93%
Target:  

HDAC

Research Areas:  

Neurological Disease

SW-100, a selective histone deacetylase 6 (HDAC6) inhibitor with an IC50 of 2.3 nM, shows at least 1000-fold selectivity for HDAC6 relative to all other HDAC isozymes. SW-100 displays a significantly improved ability to cross the blood-brain-barrier .
3
3 Cited Publications
Cat. No.: HY-P80954A
Synonyms: GAPDH; GAPD; CDABP0047; OK/SW-cl.12; Glyceraldehyde-3-phosphate dehydrogenase; Peptidyl-cysteine S-nitrosylase GAPDH

Host:  

Mouse

Application:  

WB, ELISA

Reactivity:  

Human, Mouse, Rat

3
3 Cited Publications
Cat. No.: HY-N0805
CAS No.: 26575-95-1
Synonyms: 23-Acetylalismol B; 23-O-Acetylalisol B; Alisol B monoacetate
Alisol B 23-acetate is an orally active prototerpane-type triterpenoid. Alisol B 23-acetate can be isolated from Alisma orientalis. Alisol B 23-acetate induces Apoptosis, promotes ROS generation, downregulates CDK4/6, MMP-2/9, upregulates cleaved PARP, activates FXR and inhibits Syk. Alisol B 23-acetate has anti-inflammatory and hepatoprotective activities. Alisol B 23-acetate protects the kidney from ischemia-reperfusion injury. Alisol B 23-acetate has anticancer activity against ovarian cancer, colon cancer, lung cancer, and gastric cancer. Alisol B 23-acetate can be used in the study of atherosclerosis and allergic asthma .
2
2 Cited Publications
Cat. No.: HY-129523
CAS No.: 2378258-52-5
Purity:  95.66%
Target:  

PROTACs Ras

Research Areas:  

Cancer

PROTAC K-Ras Degrader-1 (Compound 518) is a PROTAC. PROTAC K-Ras Degrader-1 can effectively degrades K-Ras based on Cereblon E3 ligand, exhibits ≥70% degradation efficacy in SW1573 cells .
1
1 Cited Publications
Cat. No.: HY-12838
CAS No.: 1386979-55-0
Purity:  99.53%
Synonyms: Mirk-IN-1; Dyrk1B/A-IN-1
Target:  

DYRK

Research Areas:  

Cancer

RO5454948 (Compound 9) is the inhibitor for Dyrk1B and Dyrk1A with IC50 of 68 nM and 22 nM. RO5454948 exhibits cytotoxicity in cancer cell SW620 with EC50 of 1.9 μM .
1
1 Cited Publications
Cat. No.: HY-124778
CAS No.: 62289-81-0
Purity:  99.74%
Target:  

Apoptosis

Research Areas:  

Cancer

SW106065 is an apoptosis inducer in malignant peripheral nerve sheath tumors (MPNST). SW106065 inhibits ATP consumption of sMPNST and other models of MPNST with an EC50 of 1 µM. SW106065 can be used for MPNST research .
1
1 Cited Publications
Cat. No.: HY-P81261
Synonyms: CTNNB1; CTNNB; OK/SW-cl.35; Catenin beta-1; Beta-catenin

Host:  

Mouse

Application:  

WB, IHC-P

Reactivity:  

Human, Mouse, Rat

1
1 Cited Publications
Cat. No.: HY-P83944
Synonyms: GAPDH; GAPD; CDABP0047; OK/SW-cl.12; Glyceraldehyde-3-phosphate dehydrogenase; Peptidyl-cysteine S-nitrosylase GAPDH

Host:  

Mouse

Application:  

WB, IHC-P, ICC/IF, FC, ELISA

Reactivity:  

Human, Mouse, Rat, Rabbit, Monkey, Pig

1
1 Cited Publications
Cat. No.: HY-148243
CAS No.: 2756014-24-9
Purity:  99.69%
Synonyms: STL5-T-0057
Research Areas:  

Cancer

IGUANA-1 free base (STL5-T-0057) is an selective ALDH1 B1 inhibitor with an IC50 value of 30 nM. IGUANA-1 free base inhibits cell growth of SW480 cells in adherent and spheroid conditions with IC50 values of 2.46 and 0.39 μM, respectively. IGUANA-1 free base can be used for the research of cancer .
1
1 Cited Publications
Cat. No.: HY-P80488
Synonyms: CTNNB, OK/SW-cl.35, PRO2286, CTNNB1, Catenin beta-1, Beta-catenin

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP, mIHC

Reactivity:  

Human, Mouse, Rat

1
1 Cited Publications
Cat. No.: HY-Q51222
CAS No.: 100264-64-0
Research Areas:  

Cancer

ZINC110492 is a selective ligand of CS-ΔEx4 (a splicing isoform of citrate synthase (CS)). ZINC110492 does not bind to CS full-length (CS-FL). ZINC110492 inhibits colorectal cancer (CRC) cell growth in cells overexpressing CS-ΔEx4 with an IC50 of 7.840 µM. ZINC110492 significantly decreases both citrate and 2-hydroxyglutarate (2-HG) levels in the CS-ΔEx4-overexpressing SW1116 cells .
1
1 Cited Publications
Cat. No.: HY-P73784
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: NA; Neuraminidase; NA/Neuraminidase Protein, H1N1 (A/Sw/Bulnes/VN1401-P6SP/2018, HEK293, His)
Species:  
Source:  
Cat. No.: HY-136302
CAS No.: 857054-02-5
Target:  

Phytohormone

Research Areas:  

Others

Karrikinolide is a plant-active compound. Karrikinolide can be extracted from smoke water (SW). Karrikinolide promotes total Cytokinin production. Plants treated with Karrikinolide exhibit superior growth in terms of rooting, leaf and bulb size, and fresh weight .
Cat. No.: HY-147058
Purity:  99.77%
Research Areas:  

Cancer

SW2_152F is a potent, selective chromobox 2 chromodomain (CBX2 ChD) inhibitor with a Kd of 80 nM. SW2_152F displays 24-1000-fold selectivity for CBX2 ChD over other CBX paralogs in vitro . SW2_152F is a click chemistry reagent, itcontains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Cat. No.: HY-138820
CAS No.: 1010820-68-4
Purity:  98.3%
Target:  

HSP

Research Areas:  

Neurological Disease

SW02 is a potent activator of ATPase activity of Hsp70, with an EC50 of 150 μM. SW02 leads to accumulation of both total tau and phosphorylated tau (pTau) .