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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
20594JTE-1511404380-58-098% Min.
20534JNJ-541754461627902-21-998% Min.
JNJ-54175446 is a potent and selective P2X7 Receptor Antagonist. JNJ-54175446 is pote
20495JC1241638611-48-998% Min.
JC124 is a NLRP3 Inflammasome Inhibitor.
20479JTE-607 HCl188791-09-598% Min.
JTE-607, also known as TO-207, is a cytokine production inhibitor potentially for the
20458JTE-0511309784-09-598% Min.
JTE-051 is a novel inhibitor of interleukin-2-inducible T cell kinase (ITK), suppress
20285JQKD822410512-38-698% Min.
JQKD82 is a cell-permeable and selective KDM5 inhibitor (MM.1S cells, IC50 = 0.42 uM)
21250JNJ-635762532110426-27-098% Min.
TRC253, also known as JNJ63576253, is a potent and orally active androgen receptor an
21247JUN901522098890-15-298% Min.
JUN90152, also known as SMS2-IN-1, is a potent and highly selective sphingomyelin syn
2091904JND32292260886-64-298% Min.
JND3229 is a New EGFRC797S Mutant Inhibitor with In Vivo Monodrug Efficacy (IC50 = 5.
2071624JMS-17-21380392-05-198% Min.
JMS-17-2 is a potent and selective antagonist of CX3CR1.
2071551JAK3-IN-21443235-95-798% Min.
JAK3-IN-2 is a potent and highly selective JAK3 inhibitor.
2071526JI0512234281-75-398% Min.
JI051 is an inhibitor of the cancer-associated transcription factor Hes1 via the PHB2
2071507JNJ-6321572510-42-998% Min.
JNJ-632 is a potent HVV capsid assembly modulator and HBV replication inhibitor with
2061305JNK-IN-71408064-71-098% Min.
JNK-IN-7 is a relatively selective JNKs inhibitor(IC50= 1.54/1.99/0.75 for JNK1/2/3);
2061305JNK-IN-71408064-71-098% Min.
204307JNJ-38877618943540-74-798% Min.
JNJ-38877618 is a hepatocyte growth factor receptor (HGFR; MET; c-Met) inhibitor pote
193292JNJ-646191782086772-26-9>98%
JNJ-64619178 is an anticancer drug candidate.
193201JNJ0966315705-75-0>98%
JNJ0966 is a highly selective allosteric inhibitor of matrix metalloproteinase-9 (MMP
184313JTE-013383150-41-2>98%
TE-013 is a potent, selective sphingosine-1-phosphate 2 (S1P2) receptor antagonist th
18381JPH203 HCl ( Nanvuranlat )1597402-27-1≧95.0%
JPH203, also known as KYT-0353, is a potent and selective LAT1 selective ( L-type ami
1711221JNJ-403465271142363-52-7>98%
JNJ-40346527 is a small molecule and orally available inhibitor of colony-stimulating
1791311JNJ-421536051254977-87-198.0%
JNJ-42153605 is a potent and selective mGlu2 receptor PAM with an acceptable pharmaco
1783012JNJ-42165279(2HCl salt)1346528-51-598.0%
JNJ-42165279 exhibited excellent ADME and pharmacodynamic properties as evidenced by
1783011JNJ-42165279(mono HCl salt)1346528-52-698.0%
JNJ-42165279 is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor. J
2017871JQ-EZ-051913252-04-698.0% 
JQ-EZ-05, also known as JQEZ5, is a bio active chemical. 
16123027JNK-IN-81410880-22-698% 
JNK-IN-8, also known as JNK Inhibitor XVI, is a selective JNK inhibitor that inhibits
16123026JNJ 635330541802326-66-498% 
JNJ 63533054 is a potent and selective GPR139 agonist (EC50 = 16 nM) that is brain an
16123025JNJ-421652791346528-50-498% 
JNJ-42165279 is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor. J
16122823JI-101900573-88-898% 
JI-101 is an orally active inhibitor of vascular endothelial growth factor receptor 2
6112701JPH203 ( KYT-0353 )1037592-40-7≧98.0%
JPH203(also known as KYT-0353) is a potent and selective LAT1 selective ( L-type amin