Others
others
Research Areas
- Actin(12)
- Inhibitory Antibodies(192)
- Adenylate cyclase(30)
- AhR(13)
- Aldose reductase(27)
- Arginase(15)
- AT Receptors(1)
- Autotaxin(4)
- ATP citrate lyase (10)
- BCRP(16)
- ROR/RAR/RXR(95)
- Caged Compounds(3)
- Calmodulin protein kinase II(1)
- CaM kinase II(9)
- Carbonic Anhydrase(30)
- Cell Penetrating Peptide(2)
- Ceramidases(4)
- CERK(1)
- Collagen proline hydroxylase(1)
- COMT(12)
- Cytokine(4)
- dCTP Pyrophosphatase(1)
- DHODH(1)
- Diacylglycerol Kinase(1)
- DNA Stain(17)
- eIF2a(2)
- Endopeptidase(3)
- Enzyme Substrates / Activators(69)
- ES-FLI1/RHA(2)
- Farnesyl Diphosphate Synthase(1)
- FBPase(5)
- FLAP(10)
- Fluorescent Probes(305)
- GLI(4)
- Glycoprotein(5)
- Glycosylase(5)
- Saccharides and Glycosides(17)
- Glyoxalase I(1)
- GSNOR(2)
- Guanylate Cyclase (32)
- Guanylyl Cyclase(7)
- Gutathione S-transferase(12)
- Heme oxygenase(10)
- Hexokinase(6)
- Hydroxylases(10)
- IL Receptor(1)
- Imidazoline Receptors(20)
- IMPDH(1)
- Inositol Phosphatases(4)
- Lp-PLA2(1)
- LpxC(1)
- Matrix Metalloprotease(1)
- MDR multidrug resistance(44)
- Menin-MLL(5)
- MGMT(1)
- Mineralocorticoid Receptor(24)
- Miscellaneous Compounds(9)
- MyD88(12)
- Myosin(29)
- NAE(2)
- NADPH Oxidase(18)
- Nampt(29)
- Natriuretic Peptide Receptors(4)
- Nitric Oxide(74)
- Nuclear Receptors(13)
- Oxygenases/Oxidases(5)
- PDHK(10)
- PGC-1α(6)
- Pregnane X Receptors(2)
- Reductases(6)
- Renin(12)
- Retinoid X Receptors(11)
- Squalene epoxidase(4)
- SGK(12)
- sFRP-1(3)
- SPHK(18)
- Synthases/Synthetases(12)
- Tachykinin(6)
- Thrombopoietin Receptor(9)
- Thymidine phosphorylase(4)
- Transcription Factors(118)
- Transketolase(3)
- β(1,3)-D-Glucan Synthase(2)
- β-Lactamase(3)
- XAO(4)
- Others(1570)
- BMI-1(1)
- SOD(9)
- Homodimerizers(2)
- Renal Diseases(9)
- FAS(24)
- calmodulin(4)
- Protein synthesis(4)
- Epac(1)
- MAGL(19)
- exocytosis(1)
- peroxiredoxins(1)
- Glucosidase(47)
- Estrogen Receptor/ERR(199)
- Progesterone Receptor(40)
- Cyclase(6)
- Environmental Toxicology(241)
- Glycerolipid Lipases(15)
- Lipases(26)
- Multidrug-Resistance Proteins(8)
- Negative Controls(9)
- Nucleic Acid Turnover/Signaling(56)
- Organ- & System-Specific Toxicity(157)
- Pesticides(102)
- Pharmaceutical Impurities(35)
- Sulfotransferases(4)
- Tec(3)
- Toxicology(161)
- Xenobiotic Sensing(23)
- UDP Glucuronosyltransferases(46)
- Amino Acid Derivatives(50)
- Drug Intermediate(265)
- Drug Isomer(60)
- Insecticide(19)
- MOFs(329)
- Phytohormone(8)
- SHMT(4)
- Phosphoramidites(28)
Products Related to Others(4271)
- GC70983THR-β agonist 5CAS: 2542029-74-1Purity: >99.00%
THR-β agonist 5 (compound 54) is a potent THR-β agonist, with an EC50 of <50 nM.
- GC71007(S)-RetosibanCAS: 2994298-20-1Purity: >99.00%
(S)-Retosiban is the isomer of Retosiban , and can be used as an experimental control.
- GC71029UCK2 Inhibitor-1CAS: 902289-98-9Purity: >96.00%
UCK2 Inhibitor-1 (Compound 20874830-2) is a non-competitive UCK2 inhibitor with an IC50 of 4.7 µM.
- GC71051OsivelotorCAS: 2417955-18-9Purity: >99.00%
Osivelotor is an allosteric modulator of haemoglobin S (HbS).
- GC71062Puromycin-bis(PEG2-amide)-BiotinCAS: 2379889-82-2Purity: >99.00%
Puromycin-bis(PEG2-amide)-Biotin is used for single-cell translatome sequencing.
- GC71065Allylic-SAMCAS: 875155-64-9
Allylic-SAM is an S-adenosyl methionine (SAM) analog for the enrichment and detection of methyltransferase target sites in RNA.
- GC71081Lobeglitazone sulfateCAS: 763108-62-9Purity: >99.00%
Lobeglitazone sulfate is a new type of thiazolidinedione.
- GC71108Nurr1 agonist 4CAS: 87645-58-7Purity: >98.00%
Nurr1 agonist 4 (compound 8) is a high-affinity Nurr1 agonist with EC50 of 2.1 μM.
- GC71193SRD5A1-IN-1CAS: 2279077-93-7Purity: >99.00%
SRD5A1-IN-1 (Compound 4) is a competitive and covalent steroid 5α-reductase type 1 (SRD5A1) inhibitor with an IC50 of 1.44 µM.
- GC71205(Rac)-ReparixinCAS: 957407-64-6Purity: >99.00%
(Rac)-Reparixin is the isomer of Reparixin , and can be used as an experimental control.
- GC71211ELOVL6-IN-4CAS: 1170321-92-2Purity: >98.00%
ELOVL6-IN-4 is a potent, selective, and orally active long chain fatty acid elongase 6 (ELOVL6) inhibitor with IC50s of 79 nM and 94 nM for human and mouse ELOVL6, respectively.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC70981 | PAL-4 | 2609594-35-4 | - | |
PAL-4 (compound 4) is a potent, selective and reversible Lysophospholipase-like 1 (LYPLAL1) activator with EC50 value of 0.39 μM and 0.49 μM for mice LYPLAL1 and huamn LYPLAL1, respectively. | ||||
| GC70983 | THR-β agonist 5 | 2542029-74-1 | >99.00% | |
THR-β agonist 5 (compound 54) is a potent THR-β agonist, with an EC50 of <50 nM. | ||||
| GC70984 | PKRA83 | 1233926-87-8 | >98.00% | |
PKRA83 (PKRA7) is a potent prokineticin (PK2) antagonist, which can compete for the binding of PK2 to its receptors PKR1 and PKR2. | ||||
| GC70997 | RAGE 229 | 2143072-85-7 | >99.00% | |
RAGE 229 is an orally active ctRAGE-DIAPH1 inhibitor. | ||||
| GC71007 | (S)-Retosiban | 2994298-20-1 | >99.00% | |
(S)-Retosiban is the isomer of Retosiban , and can be used as an experimental control. | ||||
| GC71012 | Epocholeone | 162922-31-8 | >98.00% | |
Epocholeone is a growth regulator. | ||||
| GC71020 | PG 34 | 1681056-62-1 | >98.00% | |
PG 34 is a weak O-GlcNAc transferase (OGT) inhibitor (IC50=68 μM), and a close structural analog of OSMI-1 . | ||||
| GC71025 | 20-5,14-HEDGE | 1092380-14-7 | >98.00% | |
20-5,14-HEDGE is a 20-HETE analog. | ||||
| GC71029 | UCK2 Inhibitor-1 | 902289-98-9 | >96.00% | |
UCK2 Inhibitor-1 (Compound 20874830-2) is a non-competitive UCK2 inhibitor with an IC50 of 4.7 µM. | ||||
| GC71037 | MC-PEG2-Boc | 640267-55-6 | - | |
MC-PEG2-Boc (compound 3b) is a Boc-protected Maleimide. | ||||
| GC71046 | LU-005i | 1620107-33-6 | >97.00% | |
LU-005i is a potent inhibitor of β5i subunit of immunoproteasomes (IC50 = 6.6 nM), selective over β5c subunit (IC50 = 287 nM). | ||||
| GC71048 | PTC258 | 2476724-74-8 | >98.00% | |
PTC258 is a specific and orally active splicing modulator of Elongator complex protein 1 gene (ELP1). | ||||
| GC71051 | Osivelotor | 2417955-18-9 | >99.00% | |
Osivelotor is an allosteric modulator of haemoglobin S (HbS). | ||||
| GC71062 | Puromycin-bis(PEG2-amide)-Biotin | 2379889-82-2 | >99.00% | |
Puromycin-bis(PEG2-amide)-Biotin is used for single-cell translatome sequencing. | ||||
| GC71065 | Allylic-SAM | 875155-64-9 | - | |
Allylic-SAM is an S-adenosyl methionine (SAM) analog for the enrichment and detection of methyltransferase target sites in RNA. | ||||
| GC71081 | Lobeglitazone sulfate | 763108-62-9 | >99.00% | |
Lobeglitazone sulfate is a new type of thiazolidinedione. | ||||
| GC71096 | IRF5-IN-1 | 689270-18-6 | >99.00% | |
IRF5-IN-1 (compound C5) is an IRF5 pathway-specific inhibitor. | ||||
| GC71108 | Nurr1 agonist 4 | 87645-58-7 | >98.00% | |
Nurr1 agonist 4 (compound 8) is a high-affinity Nurr1 agonist with EC50 of 2.1 μM. | ||||
| GC71145 | JNJ-1289 | 792898-18-1 | >98.00% | |
JNJ-1289 is a potent, selective, competitive and allosteric human spermine oxidase (hSMOX) inhibitor (IC50: 50 nM). | ||||
| GC71151 | LANA-DNA-IN-1 | 2512847-06-0 | >99.00% | |
LANA-DNA-IN-1 is a potent LANA-DNA inhibitor. | ||||
| GC71184 | ATF3 inducer 1 | 3038756-30-5 | >98.00% | |
ATF3 inducer 1 is a potent ATF3 inducer. | ||||
| GC71193 | SRD5A1-IN-1 | 2279077-93-7 | >99.00% | |
SRD5A1-IN-1 (Compound 4) is a competitive and covalent steroid 5α-reductase type 1 (SRD5A1) inhibitor with an IC50 of 1.44 µM. | ||||
| GC71205 | (Rac)-Reparixin | 957407-64-6 | >99.00% | |
(Rac)-Reparixin is the isomer of Reparixin , and can be used as an experimental control. | ||||
| GC71211 | ELOVL6-IN-4 | 1170321-92-2 | >98.00% | |
ELOVL6-IN-4 is a potent, selective, and orally active long chain fatty acid elongase 6 (ELOVL6) inhibitor with IC50s of 79 nM and 94 nM for human and mouse ELOVL6, respectively. | ||||