Pyrimidiner og derivater
Filtrerede søgeresultater
PROTAC BET Degrader-1, MedChemExpress
MedChemExpress PROTAC BET Degrader-1 is a PROTAC connected by ligands for Cereblon and BET, decreasing BRD2, BRD3, and BRD4 protein levels at low concentration.
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| Kemisk navn eller materiale | PROTAC BET Degrader-1 |
|---|---|
| Formel vægt | 871.9 |
| Opløselighedsinformation | DMSO : ≥ 50 mg/mL (57.35 mM) |
| Procent renhed | 98.01% |
| Fysisk form | Solid |
| Farve | Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 871.9 |
| CAS | 2093386-22-0 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | CCN1C(NC2=C3C4=CC(OC)=C(C(C(C)=NO5)=C5C)C=C4NC3=NC(C(NCCCCNC(COC6=C(C(N7C(CCC8=O)C(N8)=O)=O)C(C7=O)=CC=C6)=O)=O)=N2)=CC(C9CC9)=N1 |
| Renhedsgrad noter | Research |
| Molekylær formel | C44H45N11O9 |
| Til brug med (applikation) | Cancer-programmed cell death |
AF64394, MedChemExpress
MedChemExpress AF64394 is a GPR3 inverse agonist, with a pIC50 of 7.3.
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| Kemisk navn eller materiale | AF64394 |
|---|---|
| Sundhedsfare 1 | H302 |
| Formel vægt | 393.87 |
| Opløselighedsinformation | DMSO : ≥ 125 mg/mL (317.36 mM) |
| Procent renhed | 98.02% |
| Fysisk form | Solid |
| Farve | White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 393.87 |
| CAS | 1637300-25-4 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | ClC1=CC(OC(C)C)=C(CNC2=CC(C3=CC=CC=C3)=NC4=NC=NN42)C=C1 |
| Renhedsgrad noter | Research |
| Molekylær formel | C21H20ClN5O |
WAY-600, MedChemExpress
MedChemExpress WAY-600 is a potent, ATP-competitive, and selective mTOR inhibitor with an IC50 of 9 nM for recombinant mTOR enzyme. WAY-600 blocks mTOR complex 1/2 (mTORC1/2) assemble and activation.
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| Kemisk navn eller materiale | WAY-600 |
|---|---|
| Formel vægt | 494.59 |
| Opløselighedsinformation | DMSO : 50 mg/mL (101.09 mM; Need ultrasonic) |
| Procent renhed | 95.12% |
| Fysisk form | Solid |
| Farve | White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 494.59 |
| CAS | 1062159-35-6 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | C1(C=CN2)=C2C=CC(C3=NC(N(C4CCN(CC5=CC=CN=C5)CC4)N=C6)=C6C(N7CCOCC7)=N3)=C1 |
| Renhedsgrad noter | Research |
| Molekylær formel | C28H30N8O |
| Til brug med (applikation) | Cancer-Kinase/protease |
PRT-060318, MedChemExpress
MedChemExpress PRT-060318 (PRT318) is a novel selective inhibitor of the tyrosine kinase Syk with an IC50 of 4 nM.
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| Kemisk navn eller materiale | PRT-060318 |
|---|---|
| Formel vægt | 340.42 |
| Opløselighedsinformation | H2O : 5.6 mg/mL (16.45 mM; Need ultrasonic and warming) |
| Procent renhed | 99.04% |
| Fysisk form | Solid |
| Farve | Earth Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 340.42 |
| CAS | 1194961-19-7 |
| Synonym | PRT318 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(C1=CN=C(N[C@H]2[C@@H](N)CCCC2)N=C1NC3=CC=CC(C)=C3)N |
| Renhedsgrad noter | Research |
| Molekylær formel | C18H24N6O |
| Til brug med (applikation) | Cancer-Kinase/protease |
EED226, MedChemExpress
MedChemExpress EED226 is a polycomb repressive complex 2 (PRC2) inhibitor, which binds to the K27me3-pocket on embryonic ectoderm development (EED) and shows strong antitumor activity in xenograft mice model. EED226 is a potent, selective, and orally bioavailable EED inhibitor. EED226 inhibits PRC2 with an IC50 of 23.4 nM when the H3K27me0 peptide is used as a substrate in the in vitro enzymatic assays.
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| Kemisk navn eller materiale | EED226 |
|---|---|
| Formel vægt | 369.4 |
| Opløselighedsinformation | DMSO : ≥ 29 mg/mL (78.51 mM) |
| Procent renhed | 98.61% |
| Fysisk form | Solid |
| Farve | Off-White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 369.4 |
| CAS | 2083627-02-3 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=S(C1=CC=C(C2=CN=C(NCC3=CC=CO3)N4C2=NN=C4)C=C1)(C)=O |
| Renhedsgrad noter | Research |
| Molekylær formel | C17H15N5O3S |
| Til brug med (applikation) | Cancer-programmed cell death |
GSK2334470, MedChemExpress
MedChemExpress GSK2334470 is a highly specific and potent inhibitor of PDK1 with an IC50 of 10 nM.
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| Kemisk navn eller materiale | GSK2334470 |
|---|---|
| Sundhedsfare 1 | H302 |
| Formel vægt | 462.59 |
| Opløselighedsinformation | DMSO : ≥ 50 mg/mL (108.09 mM) |
| Procent renhed | 95.73% |
| Fysisk form | Solid |
| Farve | Light Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 462.59 |
| CAS | 1227911-45-6 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C([C@@H]1CN(C2=NC(NC)=NC(C3=CC4=C(C=C3)C(N)=NN4)=C2)[C@H](C)CC1)NC5CCCCC5 |
| Renhedsgrad noter | Research |
| Molekylær formel | C25H34N8O |
| Til brug med (applikation) | Cancer-Kinase/protease |
AZ20, MedChemExpress
MedChemExpress AZ20 is a potent and selective inhibitor of ATR with an IC50 of 5 nM, and has 8-fold selectivity against mTOR (IC50=38 nM).
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| Kemisk navn eller materiale | AZ20 |
|---|---|
| Formel vægt | 412.51 |
| Opløselighedsinformation | DMSO : ≥ 100 mg/mL (242.42 mM) |
| Procent renhed | 98.92% |
| Fysisk form | Solid |
| Farve | Off-White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 412.51 |
| CAS | 1233339-22-4 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=S(C1(C2=CC(N3[C@H](C)COCC3)=NC(C4=CC=CC5=C4C=CN5)=N2)CC1)(C)=O |
| Renhedsgrad noter | Research |
| Molekylær formel | C21H24N4O3S |
| Til brug med (applikation) | Cancer-Kinase/protease |
HJB97, MedChemExpress
MedChemExpress HJB97 is a high-affinity BET inhibitor with Kis of 0.9 nM (BRD2 BD1), 0.27 nM (BRD2 BD2), 0.18 nM (BRD3 BD1), 0.21 nM (BRD3 BD2), 0.5 nM (BRD4 BD1), 1.0 nM (BRD4 BD2), respectively. HJB97 is employed for the design of potential PROTAC BET degrader and has antitumor activity.
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| Kemisk navn eller materiale | HJB97 |
|---|---|
| Formel vægt | 500.55 |
| Opløselighedsinformation | DMSO : 30 mg/mL (59.93 mM; Need ultrasonic) |
| Procent renhed | 98.24% |
| Fysisk form | Solid |
| Farve | Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 500.55 |
| CAS | 2093391-24-1 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(C1=NC(NC2=CC(C3CC3)=NN2CC)=C4C(NC5=C4C=C(OC)C(C6=C(C)ON=C6C)=C5)=N1)NC |
| Renhedsgrad noter | Research |
| Molekylær formel | C26H28N8O3 |
| Til brug med (applikation) | Cancer-programmed cell death |
PF-06928215, MedChemExpress
MedChemExpress PF-06928215 is a cGAS (cyclic GMP-AMP Synthase) inhibitor with an IC50 of 4.9 μμ. PF-06928215 has a high binding affinity of 0.2 μM (Kd).
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VUF10460, MedChemExpress
MedChemExpress VUF10460 is a non-imidazole histamine H4 receptor agonist; binds to rat H4 receptor with a pKi of 7.46.
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| Kemisk navn eller materiale | VUF10460 |
|---|---|
| Formel vægt | 269.34 |
| Opløselighedsinformation | DMSO : 50 mg/mL (185.64 mM; Need ultrasonic) |
| Procent renhed | 98.0% |
| Fysisk form | Solid |
| Farve | Light Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 269.34 |
| CAS | 1028327-66-3 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | NC1=NC(C2=CC=CC=C2)=CC(N3CCN(C)CC3)=N1 |
| Renhedsgrad noter | Research |
| Molekylær formel | C15H19N5 |
| Til brug med (applikation) | COVID-19-immunoregulation |
ML347, MedChemExpress
MedChemExpress ML347 (LDN193719) is a highly selective ALK1/ALK2 inhibitor. ML347 has IC50 values of 46 and 32 nM against ALK1 and ALK2, respectively, >300-fold selective over ALK3. ML347 block the phosphorylation of Smad1/5 by TGF-β1.
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| Kemisk navn eller materiale | ML347 |
|---|---|
| Formel vægt | 352.39 |
| Opløselighedsinformation | DMSO : 10 mg/mL (28.38 mM; Need ultrasonic) |
| Procent renhed | 99.85% |
| Fysisk form | Solid |
| Farve | Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 352.39 |
| CAS | 1062368-49-3 |
| Synonym | LDN 193719 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | COC1=CC=C(C2=CN3C(N=C2)=C(C4=C5C=CC=NC5=CC=C4)C=N3)C=C1 |
| Renhedsgrad noter | Research |
| Molekylær formel | C22H16N4O |
| Til brug med (applikation) | Cancer-Kinase/protease |
G-749, MedChemExpress
MedChemExpress G-749 is a potent, oral active and ATP competitive FLT3 inhibitor, with IC50s of 0.4 nM and 0.6 nM for FLT3 wild type and FLT3-D835Y, respectively. G-749 can be used for the research of drug resistance for acute myeloid leukemia (AML).
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| Kemisk navn eller materiale | G-749 |
|---|---|
| Formel vægt | 521.41 |
| Opløselighedsinformation | DMSO : 25 mg/mL (47.95 mM; Need ultrasonic) |
| Procent renhed | 98.0% |
| Fysisk form | Solid |
| Farve | Off-White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 521.41 |
| CAS | 1457983-28-6 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C1C2=C(N=C(NC3CCN(C)CC3)N=C2NC4=CC=C(OC5=CC=CC=C5)C=C4)C(Br)=CN1 |
| Renhedsgrad noter | Research |
| Molekylær formel | C25H25BrN6O2 |
| Til brug med (applikation) | Cancer-Kinase/protease |
BMS-833923, MedChemExpress
MedChemExpress BMS-833923 (XL-139) is an orally bioavailable small-molecule inhibitor of Smoothened with potential antineoplastic activity; inhibits BODIPY cyclopamine binding to SMO in a dose-dependent manner with an IC50 of 21 nM.
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| Kemisk navn eller materiale | BMS-833923 |
|---|---|
| Sundhedsfare 1 | H302 |
| Formel vægt | 473.57 |
| Opløselighedsinformation | DMSO : 50 mg/mL (105.58 mM; Need ultrasonic) |
| Procent renhed | 98.21% |
| Fysisk form | Solid |
| Farve | Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 473.57 |
| CAS | 1059734-66-5 |
| Synonym | XL-139 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(NC1=CC(CNC)=CC=C1C)C2=CC=C(NC3=NC(C4=CC=CC=C4)=C5C=CC=CC5=N3)C=C2 |
| Renhedsgrad noter | Research |
| Molekylær formel | C30H27N5O |
| Til brug med (applikation) | Cancer-programmed cell death |
LDC000067, MedChemExpress
MedChemExpress LDC000067 is a highly specific CDK9 inhibitor with an IC50 value of 44±10 nM in vitro.
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| Kemisk navn eller materiale | LDC000067 |
|---|---|
| Formel vægt | 370.43 |
| Opløselighedsinformation | DMSO : ≥ 47 mg/mL (126.88 mM) |
| Procent renhed | 98.58% |
| Fysisk form | Solid |
| Farve | Off-White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 370.43 |
| CAS | 1073485-20-7 |
| Synonym | LDC067 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=S(CC1=CC=CC(NC2=NC=NC(C3=CC=CC=C3OC)=C2)=C1)(N)=O |
| Renhedsgrad noter | Research |
| Molekylær formel | C18H18N4O3S |
| Til brug med (applikation) | Cancer-Kinase/protease |
MK-8617, MedChemExpress
MedChemExpress MK-8617 is an orally active pan-inhibitor of hypoxia-inducible factor prolyl hydroxylase 1-3 (HIF PHD1-3) with an IC50 of 1 nM for PHD2.
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| Kemisk navn eller materiale | MK-8617 |
|---|---|
| Formel vægt | 443.45 |
| Opløselighedsinformation | DMSO : 6 mg/mL (13.53 mM; Need ultrasonic) |
| Procent renhed | 98.02% |
| Fysisk form | Solid |
| Farve | White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 443.45 |
| CAS | 1187990-87-9 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(C1=CN=C(C2=NN=CC=C2)N=C1O)NC(C3=CC=C(OC)C=C3)C4=CC=C(OC)C=C4 |
| Renhedsgrad noter | Research |
| Molekylær formel | C24H21N5O4 |
| Til brug med (applikation) | COVID-19-immunoregulation |