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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
128 Results for "
Less-active
" in MedChemExpress (MCE) Product Catalog:
Products (128)
128 Results for "Less-active" in MCE Product Catalog:
38
38 Publications Verification
Synonyms: Chidamide; HBI-8000; CS 055
Tucidinostat (Chidamide) is a potent and orally bioavailable HDAC enzymes class I (HDAC1/2/3) and class IIb (HDAC10) inhibitor, with IC50s of 95, 160, 67 and 78 nM, less active on HDAC8 and HDAC11 (IC50s, 733 nM, 432 nM, respectively), and shows no effect on HDAC4/5/6/7/9 .
12
12 Cited Publications
Synonyms: PF-04965842
Target:
Áreas de investigación:
Abrocitinib (PF-04965842) is a potent, orally active and selective JAK1 inhibitor, with IC50s of 29 and 803 nM for JAK1 and JAK2, respectively. Abrocitinib (PF-04965842) exhibits less active effect on TYK2 (IC50, 1.253 μM), and inhibits phosphorylation of STAT1, STAT3 and STAT5 after stimulation. Effective in autoimmune disease .
3
3 Cited Publications
Synonyms: R 55667
Áreas de investigación:
Ritanserin (R 55667) is a highly potent, relatively selective, orally active, long acting antagonist of 5-HT2 receptor, with an IC50 of 0.9 nM, less active on Histamine H1, Dopamine D2, Adrenergic α1, Adrenergic α2 receptors .
3
3 Cited Publications
Referencia número: HY-18018
No. CAS: 1242156-23-5
Target:
Áreas de investigación:
RN486 is a potent, selective and orally active Btk inhibitor with an IC50 of 4.0 nM and a Kd of 0.31 nM. RN486 is less active for other kinases. RN486 can be used for rheumatoid arthritis and systemic lupus erythematosus research .
2
2 Cited Publications
Synonyms: SU3327
Target:
Áreas de investigación:
Halicin (SU3327) is a potent, selective and substrate-competitive JNK inhibitor with an IC50 of 0.7 μM. Halicin also inhibits protein-protein interactions between JNK and JNK Interacting Protein (JIP) with an IC50 of 239 nM. Halicin shows less active against p38α and Akt kinase .
2
2 Cited Publications
Synonyms: (S)-TR 700; (S)-DA 7157
Target:
Áreas de investigación:
(S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens. (S)-Tedizolid is the less active isomer.
1
1 Cited Publications
Referencia número: HY-A0295
No. CAS: 13071-11-9
Target:
Áreas de investigación:
(R)-Propranolol hydrochloride is a less active enantiomer of the β-adrenoceptor antagonist propranolol (HY-B0573). Propranolol is a nonselective β-adrenergic receptor (βAR) antagonist, has high affinity for the β1AR and β2AR with Ki values of 1.8 nM and 0.8 nM, respectively .
1
1 Cited Publications
Synonyms: KPT-8602 (Z-isomer)
Eltanexor Z-isomer (KPT-8602 Z-isomer) is the less active isomer of KPT-8602.
1
1 Cited Publications
Target:
Áreas de investigación:
GSK9311, a less active analogue of GSK6853, can be used as a negative control. GSK9311 inhibits BRPF bromodomain with pIC50 values of 6.0 and 4.3 for BRPF1 and BRPF2, respectively .
1
1 Cited Publications
Target:
Áreas de investigación:
DCLX069 is a selective protein arginine methyltransferase 1 (PRMT1) inhibitor with an IC50 value of 17.9 µM. DCLX069 shows less active against PRMT4 and PRMT6. DCLX069 has anticancer effects .
1
1 Cited Publications
Referencia número: HY-N1778A
No. CAS: 14737-89-4
Synonyms: (E)-O-Methylferulic acid
1
1
1 Cited Publications
Target:
Áreas de investigación:
(S)-TXNIP-IN-1 is the less active S-enantiomer of TXNIP-IN-1 (HY-115688). TXNIP-IN-1 is a TXNIP-TRX complex inhibitor which can be used in the research of TXNIP-TRX complex associated metabolic disorder (diabetes), cardiovascular disease, or inflammatory disease
1
1 Cited Publications
Referencia número: HY-19908B
No. CAS: 2446175-39-7
Target:
Áreas de investigación:
(R)-BAY-85-8501 is the less active Enantiomer of BAY-85-8501. BAY-85-8501 is a selective and potent inhibitor of Human Neutrophil Elastase (HNE), with an IC50 of 65 pM .
Synonyms: ONO-6818; ONO-PO-736
Target:
Áreas de investigación:
Freselestat (ONO-6818) is a potent and orally active neutrophil elastase inhibitor with a Ki of 12.2 nM. Freselestat is >100-fold less-active against other proteases such as trypsin, protein-ase 3, pancreatic elastase, plasmin, thrombin, collagenase, cathepsin G, and murine macrophage elastase. Freselestat has a potent anti-inflammatory activity .
Synonyms: (-)-MK-801 maleate
Target:
Áreas de investigación:
(-)-Dizocilpine maleate ((-)-MK-801 maleate) is a less active (-)-enantiomer of Dizocilpine. (-)-Dizocilpine maleate is a selective and non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist with a Ki of 211.7 nM. (-)-Dizocilpine maleate has antidepressant effects .
Referencia número: HY-W074930
No. CAS: 147127-19-3
Synonyms: (S)-GS 1278; (S)-PMPA; (S)-TDF
(S)-Tenofovir is the less active S-enantiomer of Tenofovir (HY-13910). Tenofovir is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B (HBV). (S)-Tenofovir has low activity to Orf virus. (S)-Tenofovir can be used for research on contagious pustular dermatitis .
Referencia número: HY-17044A
No. CAS: 1261590-48-0
Synonyms: IPI-145 R enantiomer; INK1197 R enantiomer
Duvelisib R enantiomer is a PI3K inhibitor, which is the less active enantiomer of Duvelisib.
Referencia número: HY-16950B
No. CAS: 174592-47-3
Synonyms: (E)-Afimoxifene
Target:
Áreas de investigación:
(E)-4-Hydroxytamoxifen ((E)-Afimoxifene), the less active isomer of (Z)-4-hydroxytamoxifen, is an estrogen receptor modulator.
Referencia número: HY-40354D
No. CAS: 1092578-46-5
Target:
Áreas de investigación:
(3R,4S)-Tofacitinib is an less active enantiomer of Tofacitinib. Tofacitinib inhibits JAK3 with IC50 of 1 nM.
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
