Research Chemicals - suppliers, manufacturers, exporters


Crenolanib(CP-868596) LAB GRADE 97%

Crenolanib(CP-868596) can inhibit PDGFR-alpha with IC50 of 10 nM. More information please visit the website:

Cys(Npys)-TAT (47-57) LAB GRADE 97%

This peptide corresponds to the protein transduction domain of the TAT protein and is synthesized with an activated cysteine residue C(Npys), wherein Npys is 3-Nitro-2-pyridinesulfenyl group and is used for activating S of cysteine and for rapid reaction when a thiol group is introduced. This kind of modification has been used to render this peptide as a cell penetrating and carrier peptide applicable in conjugation studies.

DCC-2036 (Rebastinib) LAB GRADE 97%

Creative Enzymes uses its expertise in enzyme manufacturing to supply customers enzymes using for life science research and production of medicines, food, alcohol, beer, fruit juice, fabric, paper, leather goods, etc. We provide DCC-2036 (Rebastinib). More information please visit the website:

Empagliflozin Enantiomer Impurity

Impurity in commercial preparation of Empagliflozin.

INDENO[1,2,3-CD]PYRENE (D12, 98%)

Name INDENO[1,2,3-CD]PYRENE (D12, 98%)
Cat# CPIL100189
Unlabeled CAS# 193-39-5
Labeled CAS# NA
Chemical Formula C22D12
Molecular Weight 288.42
Chemical Purity 0.99

LY315920(Varespladib) LAB GRADE 97%

LY315920(Varespladib) More information please visit the website:

Levocetirizine D4 Dihydrochloride

Molecular formula: C21H23D4Cl3N2O3
Molecular weight: 465.83

N-Desmethyl Nefopam Hydrochloride

Molecular Formula: C16H17NOHCl

O-β-D-Glucosylgentiopicroside, 6'-

?Product Name? O-?-D-Glucosylgentiopicroside, 6'- ?CAS Number? 115713-06-9 ?Synonyms? 6'-O-?-D-Glucopyranosylgentiopicroside ?Chemical Name? 1H,3H-Pyrano[3,4-c]pyran-1-one,5-ethenyl-6-[(6-O-?-D-glucopyranosyl-?-D-glucopyranosyl)oxy]-5,6-dihydro-,(5R,6S)- ?Chemical Formula? C22H30O14 ?Molecular Weight? 518.47 ?Chemotaxonomic Group? Terpenoids ?Product Number? PS0329-0020 ?Grade? ?98.5% (LC&T) ?Size? 20mg

PF-05212384 (PKI-587) LAB GRADE 97%

As an ATP-competitive inhibitor, PKI-587 can potently inhibited PI3K-alpha and mTOR with of 0.4 nM and 1 nM. More information please visit the website:

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