Isotope Standards
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Filtered Search Results
MMAF-d8 hydrochloride, MedChemExpress
MedChemExpress D8-MMAF hydrochloride is a deuterated form of MMAF hydrochloride, which is a microtubule disrupting agent.
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Molecular Weight (g/mol) | 776.47 |
---|---|
Color | Off-White |
Physical Form | Solid |
Chemical Name or Material | MMAF-d8 hydrochloride |
Grade | Research |
SMILES | CC[C@H](C)[C@@H]([C@@H](CC(N1[C@@H](CCC1)[C@@H]([C@@H](C)C(N[C@H](C(O)=O)CC2=CC=CC=C2)=O)OC)=O)OC)N(C([C@@](C([2H])(C([2H])([2H])[2H])C([2H])([2H])[2H])([2H])NC([C@H](C(C)C)NC)=O)=O)C.Cl |
For Use With (Application) | Cancer-programmed cell death |
Percent Purity | 98.97% |
Solubility Information | DMSO : 100 mg/mL (128.79 mM; Need ultrasonic) |
Purity Grade Notes | Research |
Recommended Storage | 4°C, sealed storage, away from moisture∣The compound is unstable in solutions, freshly prepared is recommended. |
Shelf Life | 4°C, sealed storage, away from moisture∣The compound is unstable in solutions, freshly prepared is recommended. |
Molecular Formula | C39H58D8ClN5O8 |
Formula Weight | 776.47 |
Banoxantrone-d12 dihydrochloride, MedChemExpress
MedChemExpress Banoxantrone-d12 (AQ4N-d12) dihydrochloride is the deuterium labeled Banoxantrone dihydrochloride. Banoxantrone is a novel bioreductive agent that can be reduced to a stable, DNA-affinic compound AQ4, which is a potent topoisomerase II inhibitor.
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Molecular Weight (g/mol) | 529.48 |
---|---|
Color | Blue |
Physical Form | Solid |
Chemical Name or Material | Banoxantrone-d12 dihydrochloride |
Grade | Research |
SMILES | O=N(C([2H])([2H])[2H])(C([2H])([2H])[2H])CCNC1=CC=C(NCCN(C([2H])([2H])[2H])(C([2H])([2H])[2H])=O)C(C(C2=C(O)C=CC(O)=C23)=O)=C1C3=O.Cl.Cl |
For Use With (Application) | Cancer-programmed cell death |
Percent Purity | 98.02% |
CAS | 1562066-98-1 |
Synonym | AQ4N-d12 dihydrochloride |
Purity Grade Notes | Research |
Recommended Storage | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
Shelf Life | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
Molecular Formula | C22H18D12Cl2N4O6 |
Formula Weight | 529.48 |
VD3-d6, MedChemExpress
MedChemExpress VD3-d6 (Vitamin D3-26,26,26,27,27,27-d6) is the deuterium labeled Vitamin D3; tools for determination of Vitamin D3 metabolites in human serum.
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Molecular Weight (g/mol) | 390.67 |
---|---|
Color | Light Yellow |
Physical Form | Solid |
Chemical Name or Material | VD3-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])C)([H])[C@]3(C)CCC\2 |
For Use With (Application) | Neuroscience-Neuromodulation |
Percent Purity | 98.0% |
CAS | 118584-54-6 |
Solubility Information | DMSO : 100 mg/mL (255.97 mM; Need ultrasonic) |
Synonym | Vitamin D3-26,26,26,27,27,27-d6 |
Purity Grade Notes | Research |
Recommended Storage | -20°C, protect from light, stored under nitrogen∣The compound is unstable in solutions, freshly prepared is recommended. |
Shelf Life | -20°C, protect from light, stored under nitrogen∣The compound is unstable in solutions, freshly prepared is recommended. |
Molecular Formula | C27H38D6O |
Formula Weight | 390.67 |
Netupitant-d6, MedChemExpress
MedChemExpress Netupitant D6 is the deuterium labeled Netupitant (CID-6451149), which is a highly potent and selective, orally active neurokinin-1 (NK1) receptor antagonist.
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Mycophenolic acid-d3, MedChemExpress
MedChemExpress Mycophenolic acid D3 (Mycophenolate D3) is deuterium labeled Mycophenolic acid, which is an an immunosuppresant drug and has potent anti-proliferative activity.
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Molecular Weight (g/mol) | 323.36 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | Mycophenolic acid-d3 |
Grade | Research |
SMILES | O=C(OC1)C2=C1C(C)=C(OC([2H])([2H])[2H])C(C/C=C(C)/CCC(O)=O)=C2O |
Percent Purity | 98.0% |
CAS | 1185242-90-3 |
Synonym | Mycophenolate-d3 |
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 | C17H17D3O6 |
Formula Weight | 323.36 |
Calcitriol-d6, MedChemExpress
MedChemExpress Calcitriol-d6 is the deuterium labeled Calcitriol. Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
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Nitazoxanide-d4, MedChemExpress
MedChemExpress Nitazoxanide D4 (NTZ D4) is the deuterium labeled Nitazoxanide, which is an antiprotozoal agent.
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Molecular Weight (g/mol) | 311.31 |
---|---|
Color | Off-White |
Physical Form | Solid |
Chemical Name or Material | Nitazoxanide-d4 |
Grade | Research |
SMILES | O=C(NC1=NC=C([N+]([O-])=O)S1)C2=C(OC(C)=O)C([2H])=C([2H])C([2H])=C2[2H] |
Percent Purity | 98.0% |
CAS | 1246819-17-9 |
Synonym | NTZ-d4 NSC-697855-d4 |
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 | C12H5D4N3O5S |
Formula Weight | 311.31 |
Pyridostigmine-d6 bromide, MedChemExpress
MedChemExpress Pyridostigmine D6 bromide is the deuterium labeled Pyridostigmine, which is a parasympathomimetic and a reversible cholinesterase inhibitor.
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Molecular Weight (g/mol) | 267.15 |
---|---|
Color | White |
Physical Form | Solid |
Chemical Name or Material | Pyridostigmine-d6 bromide |
Grade | Research |
SMILES | O=C(N(C([2H])([2H])[2H])C([2H])([2H])[2H])OC1=CC=C[N+](C)=C1.[Br-] |
Percent Purity | 98.0% |
CAS | 2375858-08-3 |
Solubility Information | DMSO : 50 mg/mL (187.16 mM; Need ultrasonic) |
Purity Grade Notes | Research |
Recommended Storage | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
Shelf Life | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
Molecular Formula | C9H7D6BrN2O2 |
Formula Weight | 267.15 |
PSI-6206 13C,d3, MedChemExpress
MedChemExpress PSI-6206 13CD3 is the deuterium labeled PSI-6206. PSI-6206 is the deaminated derivative of PSI-6130, which is a potent and selective inhibitor of HCV NS5B polymerase. PSI-6206 low potently inhibits HCV replicon with EC90 of >100 μM.
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Molecular Weight (g/mol) | 264.23 |
---|---|
Color | Light Yellow |
Physical Form | Solid |
Chemical Name or Material | PSI-6206 13C,d3 |
Grade | Research |
SMILES | OC[C@@H]1[C@H]([C@@]([13C]([2H])([2H])[2H])(F)[C@H](N2C(NC(C=C2)=O)=O)O1)O |
Percent Purity | 98.0% |
CAS | 1256490-42-2 |
Synonym | RO-2433 13C,d3 GS-331007 13C,d3 Sofosbuvir metabolite GS-331007 13C,d3 |
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 | C9 13CH10D3FN2O5 |
Formula Weight | 264.23 |
Omeprazole-d3, MedChemExpress
MedChemExpress Omeprazole-d3 (H 16868-d3) is deuterium labeled Omeprazole. Omeprazole, a proton pump inhibitor (PPI), is available for treatment of acid-related gastrointestinal disorders. Omeprazole shows competitive inhibition of CYP2C19 activity with a Ki of 2 to 6 μM. Omeprazole also inhibits growth of Gram-positive and Gram-negative bacteria.
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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.
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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 |
(±)-Levomepromazine-d6, MedChemExpress
MedChemExpress (±)-Levomepromazine D6 ((±)-Methotrimeprazine D6) is the deuterium labeled Methotrimeprazine, which is a D3 dopamine and Histamine H1 receptor antagonist.
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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.
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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 |