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Filtered Search Results
Eldecalcitol-d6, MedChemExpress
MedChemExpress Eldecalcitol-d6 is the deuterium labeled Eldecalcitol. Eldecalcitol is an orally active analogue of active vitamin D used in the treatment of osteoporosis.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Fexofenadine-d6, MedChemExpress
MedChemExpress Fexofenadine D6 (MDL-16455 D6) is deuterium labeled is Fexofenadine, which is an antihistamine pharmaceutical agent.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Molecular Weight (g/mol) | 507.69 |
---|---|
Color | White |
Physical Form | Powder |
Chemical Name or Material | Fexofenadine-d6 |
Grade | Research |
SMILES | OC(C1=CC=CC=C1)(C2=CC=CC=C2)C3CCN(CCCC(C4=CC=C(C(C(O)=O)(C([2H])([2H])[2H])C([2H])([2H])[2H])C=C4)O)CC3 |
For Use With (Application) | Neuroscience-Neuromodulation |
Percent Purity | 98.0% |
CAS | 548783-71-7 |
Synonym | MDL-16455-d6 Terfenadine carboxylate-d6 |
Purity Grade Notes | Research |
Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
Molecular Formula | C32H33D6NO4 |
Formula Weight | 507.69 |
Azilsartan-d5, MedChemExpress
MedChemExpress Azilsartan D5 (TAK-536 D5) is the deuterium labeled Azilsartan(TAK-536), which is a specific and potent angiotensin II type 1 receptor antagonist.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Molecular Weight (g/mol) | 461.48 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | Azilsartan-d5 |
Grade | Research |
SMILES | OC(C1=CC=CC2=C1N(C(OC(C([2H])([2H])[2H])([2H])[2H])=N2)CC(C=C3)=CC=C3C4=CC=CC=C4C5=NC(ON5)=O)=O |
Percent Purity | 98.0% |
CAS | 1346599-45-8 |
Synonym | TAK-536-d5 |
Purity Grade Notes | Research |
Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
Molecular Formula | C25H15D5N4O5 |
Formula Weight | 461.48 |
Sofosbuvir-d6, MedChemExpress
MedChemExpress Sofosbuvir D6 (PSI-7977 D6) is the deuterium labeled Sofosbuvir. Sofosbuvir (PSI-7977) is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Molecular Weight (g/mol) | 535.49 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | Sofosbuvir-d6 |
Grade | Research |
SMILES | O=C1N([C@H]2[C@]([C@H](O)[C@@H](CO[P@](OC3=CC=CC=C3)(N[C@@H](C)C(OC(C([2H])([2H])[2H])C([2H])([2H])[2H])=O)=O)O2)(C)F)C=CC(N1)=O |
Percent Purity | 95.0% |
CAS | 1868135-06-1 |
Synonym | PSI-7977-d6 GS-7977-d6 |
Purity Grade Notes | Research |
Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
Molecular Formula | C22H23D6FN3O9P |
Formula Weight | 535.49 |
MMAD-d8, MedChemExpress
MedChemExpress D8-MMAD is a deuterated form of MMAD, which is a microtubule disrupting agent.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Molecular Weight (g/mol) | 779.11 |
---|---|
Color | Off-White |
Physical Form | Solid |
Chemical Name or Material | MMAD-d8 |
Grade | Research |
SMILES | O=C(N[C@H](C1=NC=CS1)CC2=CC=CC=C2)[C@H](C)[C@@H](OC)[C@H]3N(C(C[C@@H](OC)[C@H]([C@@H](C)CC)N(C([C@@](C([2H])(C([2H])([2H])[2H])C([2H])([2H])[2H])([2H])NC([C@H](C(C)C)NC)=O)=O)C)=O)CCC3 |
For Use With (Application) | Cancer-programmed cell death |
Percent Purity | 99.12% |
Solubility Information | DMSO : ≥ 100 mg/mL (128.35 mM) |
Synonym | Demethyldolastatin 10-d8 Monomethylauristatin D-d8 Monomethyl Dolastatin 10-d8 |
Purity Grade Notes | Research |
Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣The compound is unstable in solutions, freshly prepared is recommended. |
Shelf Life | Powder -20°C 3 years, 4°C 2 years∣The compound is unstable in solutions, freshly prepared is recommended. |
Molecular Formula | C41H58D8N6O6S |
Formula Weight | 779.11 |
(±)-Levomepromazine-d6, MedChemExpress
MedChemExpress (±)-Levomepromazine D6 ((±)-Methotrimeprazine D6) is the deuterium labeled Methotrimeprazine, which is a D3 dopamine and Histamine H1 receptor antagonist.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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25-Hydroxy VD2-d6, MedChemExpress
MedChemExpress 25-Hydroxy VD2-d6 is the deuterium labeled 25-Hydroxy VD2.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Molecular Weight (g/mol) | 418.68 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | 25-Hydroxy VD2-d6 |
Grade | Research |
SMILES | O[C@@H](CCC/1=C)CC1=C\C=C2[C@@](CC[C@@H]3[C@@H](/C=C/[C@H](C)C(C([2H])([2H])[2H])(C([2H])([2H])[2H])O)C)([H])[C@]3(C)CCC\2 |
Percent Purity | 98.96% |
CAS | 1262843-46-8 |
Solubility Information | DMSO : 100 mg/mL (238.85 mM; Need ultrasonic) |
Purity Grade Notes | Research |
Recommended Storage | 4°C, protect from light, stored under nitrogen∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light, stored under nitrogen) |
Shelf Life | 4°C, protect from light, stored under nitrogen∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light, stored under nitrogen) |
Molecular Formula | C28H38D6O2 |
Formula Weight | 418.68 |
1alpha, 25-Dihydroxy VD2-d6, MedChemExpress
MedChemExpress 1alpha, 25-Dihydroxy VD2-D6 is a deuterated form of vitamin D.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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CAS | 216244-04-1 |
---|---|
Molecular Weight (g/mol) | 434.68 |
Chemical Name or Material | 1alpha, 25-Dihydroxy VD2-d6 |
Grade | Research |
SMILES | O[C@H](C/1=C)C[C@H](O)CC1=C\C=C2[C@@](CC[C@@H]3[C@@H](/C=C/[C@H](C)C(C([2H])([2H])[2H])(C([2H])([2H])[2H])O)C)([H])[C@]3(C)CCC\2 |
Purity Grade Notes | Research |
Recommended Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Shelf Life | Please store the product under the recommended conditions in the Certificate of Analysis. |
For Use With (Application) | Metabolism-sugar/lipid metabolism |
Molecular Formula | C28H38D6O3 |
Formula Weight | 434.68 |
Calcifediol-d6, MedChemExpress
MedChemExpress Calcifediol-d6 is the deuterium labeled Calcifediol. Calcifediol, a major circulating metabolite of vitamin D3, is a potent VDR inhibitor.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Molecular Weight (g/mol) | 406.67 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | Calcifediol-d6 |
Grade | Research |
SMILES | O[C@@H](CCC/1=C)CC1=C\C=C2[C@@](CC[C@@H]3[C@@H](CCCC(C([2H])([2H])[2H])(C([2H])([2H])[2H])O)C)([H])[C@]3(C)CCC\2 |
For Use With (Application) | Metabolism-sugar/lipid metabolism |
Percent Purity | 98.0% |
CAS | 78782-98-6 |
Purity Grade Notes | Research |
Recommended Storage | -20°C, protect from light, stored under nitrogen∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light, stored under nitrogen) |
Shelf Life | -20°C, protect from light, stored under nitrogen∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light, stored under nitrogen) |
Molecular Formula | C27H38D6O2 |
Formula Weight | 406.67 |
Cycloguanil-d6, MedChemExpress
MedChemExpress Cycloguanil D6 is the deuterium labeled Cycloguanil, which is a dihydrofolate reductase inhibitor.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Irbesartan-d4, MedChemExpress
MedChemExpress Irbesartan D4 is the deuterium labeled Irbesartan, which is a highly potent and specific angiotensin II type 1 (AT1) receptor antagonist.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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VX-984, MedChemExpress
MedChemExpress VX-984 (M9831) is an orally active, potent, selective and BBB-penetrated DNA-PK inhibitor. VX-984 efficiently inhibits NHEJ (non-homologous end joining) and increases DSBs (DNA double-strand breaks). VX-984 can be used for glioblastomas (GBM) and non-small cell lung cancer (NSCLC) research.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Molecular Weight (g/mol) | 415.49 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | VX-984 |
Grade | Research |
SMILES | O=C(C1=CC=NC2=C([C@H](C)CNC3=CC(C4=C([2H])N=C(C)N=C4[2H])=NC=N3)C=CC=C12)NC |
For Use With (Application) | Cancer-Kinase/protease |
Percent Purity | 98.34% |
CAS | 1476074-39-1 |
Solubility Information | DMSO : 10 mg/mL (24.07 mM; Need ultrasonic) |
Synonym | M9831 |
Purity Grade Notes | Research |
Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
Molecular Formula | C23H21D2N7O |
Formula Weight | 415.49 |