10130 Results for "

HF/6-31G basis set

" in MedChemExpress (MCE) Product Catalog:
Products (10130)

10130 Results for "HF/6-31G basis set" in MCE Product Catalog:

14
14 Publications Verification
Cat. No.: HY-18627A
CAS No.: 1627607-87-7
Synonyms: (R)-PFI-2 hydrochloride
PFI-2 ((R)-PFI-2 hydrochloride) hydrochloride is a potent and selective SET domain containing lysine methyltransferase 7 (SETD7) inhibitor. (R)-PFI-2 shows high inhibiting activity with IC50 value of 2.0  nM and (S)-PFI-2 shows inhibiting activity with IC50  value of 1.0  μM. PFI-2 hydrochloride can be used for the research of chronic kidney disease and inflammation response in the development of renal fibrosis .
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14
14 Publications Verification
Cat. No.: HY-18627
CAS No.: 1627676-59-8
Synonyms: (R)-PFI-2
PFI-2 ((R)-PFI-2 hydrochloride) hydrochloride, a chemical probe, is a potent and selective SET domain containing lysine methyltransferase 7 (SETD7) inhibitor. (R)-PFI-2 shows high inhibiting activity with IC50 value of 2.0 nM and (S)-PFI-2 shows inhibiting activity with IC50 value of 1.0 μM. PFI-2 hydrochloride can be used for the research of chronic kidney disease and inflammation response in the development of renal fibrosis .
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9
9 Cited Publications
Cat. No.: HY-100359
CAS No.: 307002-71-7
Purity:  99.71%
Target:  

MMP

Research Areas:  

Inflammation/Immunology Cancer

CL-82198 is a selective inhibitor of MMP-13. CL-82198 binds to the entire S1’ pocket of MMP-13, which is the basis for its selectivity towards MMP-13 and the lack of inhibitory activities against other MMPs . CL-82198 is a pharmacologic treatment for preventing osteoarthritis (OA) progression .
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6
6 Cited Publications
Cat. No.: HY-141539A
Purity:  99.77%
Research Areas:  

Cancer

SETDB1-TTD-IN-1 TFA is a potent, selective and endogenous binder competitive ligand of SET domain bifurcated protein 1 tandem tudor domain (SETDB1-TTD) that binds to TTD, with a Kd of 88 nM. SETDB1-TTD-IN-1 TFA increases SETDB1 methyltransferase activity. SETDB1-TTD-IN-1 TFA can be used for the research of biological functions and disease associations of SETDB1-TTD .
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5
5 Cited Publications
Cat. No.: HY-N3584
CAS No.: 68124-04-9
Synonyms: Chonglou Saponin VII
Paris saponin VII (Chonglou Saponin VII) is a steroidal saponin isolated from the roots and rhizomes of Trillium tschonoskii. Paris saponin VII-induced apoptosis in K562/ADR cells is associated with Akt/MAPK and the inhibition of P-gp. Paris saponin VII attenuates mitochondrial membrane potential, increases the expression of apoptosis-related proteins, such as Bax and cytochrome c, and decreases the protein expression levels of Bcl-2, caspase-9, caspase-3, PARP-1, and p-Akt. Paris saponin VII induces a robust autophagy in K562/ADR cells and provides a biochemical basis in the treatment of leukemia .
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4
4 Cited Publications
Cat. No.: HY-16478
CAS No.: 733030-01-8
Synonyms: TAS-102; FTD/TPI
Trifluridine/tipiracil hydrochloride mixture (TAS-102) is a potent and orally active nucleoside antitumor agent. The composition of Trifluridine/tipiracil hydrochloride mixture (TAS-102) is a 1:0.5 mixture (on a molar basis) of alpha,alpha,alpha-tri-fluorothymidine (FTD) and thymidine phosphorylase inhibitor (TPI). Trifluridine/tipiracil hydrochloride mixture (TAS-102) shows the antitumor activity mainly via the inhibition of thymidylate synthase (TS) and incorporation into DNA .
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2
2 Cited Publications
Cat. No.: HY-132222
CAS No.: 2313525-20-9
Purity:  99.78%
Target:  

TRP Channel

Research Areas:  

Cancer

SET2 is a selective TRPV2 antagonist (IC50=0.46 μM). SET2 blocks the TRP channel and suppresses prostate cancer cells migration. SET2 reduces the lysophosphatidic acid (LPA, a TRPV2 activator)-induced cytoplasmic calcium increases .
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2
2 Cited Publications
Cat. No.: HY-P74394
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: VTCN1; V‑set Domain Containing T Cell Activation Inhibitor 1; B7‑H4; B7H4; B7h.5; B7S1; B7x; V‑set Domain‑Containing T‑Cell Activation Inhibitor 1; Immune Costimulatory Protein B7‑H4; B7 Superfamily Member 1; B7 Family Member, H4; B7 Homolog 4; FLJ22418;
Species:  
Mouse
Source:  
HEK293
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1
1 Cited Publications
Cat. No.: HY-154812
CAS No.: 2604513-16-6
Purity:  99.81%
Synonyms: KTX-1001
Research Areas:  

Cancer

Gintemetostat (KTX-1001) is an orally active, highly specific NSD2/MMSET histone methyltransferase inhibitor with human NSD2 IC50 values ranging 0.460-2.17 nM and NSD2 SET domain IC50 of 2.32 nM and Kd values ranging 6.3-70.4 nM .Gintemetostat reduces H3K36me2 levels, impairs multiple myeloma cell adhesion and colony formation, enhances cytotoxicity, boosts T-cell activation, and sensitizes resistant multiple myeloma cells to other agents .Gintemetostat can be used for the research of multiple myeloma and relapsed and refractory multiple myeloma .
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1
1 Cited Publications
Cat. No.: HY-138283
CAS No.: 1210906-48-1
Purity:  99.82%
Research Areas:  

Cancer

MR837 is an inhibitor of NSD2-PWWP1. MR837 can bind with human nuclear receptor binding SET domain protein 2 (PWWP domain) .
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1
1 Cited Publications
Cat. No.: HY-P76079
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: SMYD2; Histone Methyltransferase SMYD2; set And MYND Domain Containing 2; ZMYND14; HSKM-B; Lysine N-Methyltransferase 3C; KMT3C; [Histone H3]-Lysine(4) N-Trimethyltransferase; set And MYND Domain-Containing Protein 2; Zinc Finger, MYND Domain Containing 1
Species:  
Human
Source:  
Sf9 insect cells
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1
1 Cited Publications
Cat. No.: HY-P72428
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: VSIR; V‑set Immunoregulatory Receptor; C10orf54; SISP1; VISTA; B7‑H5; PD‑1H; Dies1; GI24; B7H5; V‑Type Immunoglobulin Domain‑Containing Suppressor Of T‑Cell Activation; V‑set Domain‑Containing Immunoregulatory Receptor; V‑Domain Ig Suppressor Of T Cell Ac
Species:  
Mouse
Source:  
HEK293
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1
1 Cited Publications
Cat. No.: HY-P74395
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: VTCN1; V‑set Domain Containing T Cell Activation Inhibitor 1; B7‑H4; B7H4; B7h.5; B7S1; B7x; V‑set Domain‑Containing T‑Cell Activation Inhibitor 1; Immune Costimulatory Protein B7‑H4; B7 Superfamily Member 1; B7 Family Member, H4; B7 Homolog 4; FLJ22418;
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-Y1220D
CAS No.: 584-08-7
Anhydrous potassium carbonate, 99.995% metals basis is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-139452
CAS No.: 209540-62-5
Purity:  99.96%
Target:  

Glycosidase

Research Areas:  

Others

PFB-FDGlu is a selective lysosomal Glucocerebrosidase (GCase) substrate, which is metabolised by GCase to yield fluorescein. PFB-FDGlu is cell permeable and can be used with a flow cytometer to measure GCase activity in living cells on a single-cell basis .
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Cat. No.: HY-ER013B
CAS No.: 497-19-8
Synonyms: Calcined soda 99.999% trace metals basis
Sodium carbonate anhydrous, 99.999% trace metals basis is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-W011517
CAS No.: 146-78-1
Synonyms: 2FA
2-Fluoroadenosine (2FA) is a nucleoside analogue. 2-Fluoroadenosine has antiparasite activity with EC50 value of 0.842 mM for Cryptosporidium parvum. 2-Fluoroadenosine has a highly specific structural basis for MtADK. 2-Fluoroadenosine is commonly used in the study of parasitic conditions .
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Cat. No.: HY-W003969
CAS No.: 695-34-1
Synonyms: Ascensil; 2-Amino-4-methylpyridine
Target:  

NO Synthase

Research Areas:  

Inflammation/Immunology

Aminopicoline (Ascensil) is a potent and non-selective inhibitor of nitric oxide synthase (NOS) isoenzymes (iNOS, nNOS, eNOS). Aminopicoline competes with arginine at the substrate-binding site of nitric oxide synthase, reduces cellular nitric oxide production, inhibits the elevation of plasma nitrate, increases mean arterial pressure at high doses, and also serves as a basis for radiolabeled ligands to localize nitric oxide synthase binding sites. Aminopicoline can be used in the research of diseases associated with septic shock, joint inflammation, intestinal inflammation, and CNS inflammation .
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Cat. No.: HY-B1817A
CAS No.: 557-34-6
Synonyms: Zinc(II) acetate, 99.99% trace metals basis
Zinc (Zinc (II)) acetate, 99.99% trace metals basis is a heme oxygenase 1 (HO-1) activator and apoptosis inducer with cytotoxic and anticancer activities. Zinc acetate, 99.99% trace metals basis enhances HO-1 expression, alters the microRNA profile, and increases the level of caspase-cleaved cytokeratin 18. Zinc acetate, 99.99% trace metals basis also regulates the expression of Cdk2/cyclin E and interferes with cell cycle progression. Zinc acetate, 99.99% trace metals basis effectively inhibits cancer cell proliferation and induces their rapid death, with no significant cytotoxicity to non-tumor tissues. Zinc acetate, 99.99% trace metals basis has been widely used in studies related to hepatocellular carcinoma, prostate cancer, and other conditions .
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Cat. No.: HY-Y0537C
CAS No.: 7447-40-7
Synonyms: Potassium chloride, suitable for the extraction and solubilization of proteins
Potassium chloride, ≥99.99% trace metals basis (Potassium chloride, suitable for the extraction and solubilization of proteins), is an inorganic salt used in the preparation of phosphate buffers. With very low metal impurity content, it is suitable for protein extraction and dissolution.
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