Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C62H88N13O14P.Co.ClH.HO |
| Molecular Weight | 1382.816 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 13 / 14 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[OH-].Cl.[Co+3].C[C@H](CNC(=O)CC[C@]1(C)[C@@H](CC(N)=O)C2[N-]C1=C(C)C3=NC(=CC4=NC(=C(C)C5=N[C@]2(C)[C@@](C)(CC(N)=O)[C@@H]5CCC(N)=O)[C@@](C)(CC(N)=O)[C@@H]4CCC(N)=O)C(C)(C)[C@@H]3CCC(N)=O)OP([O-])(=O)O[C@@H]6[C@@H](CO)O[C@@H]([C@@H]6O)N7C=NC8=C7C=C(C)C(C)=C8
InChI
InChIKey=KEHNCSYXYMMUCO-FBTIOKFQSA-K
InChI=1S/C62H90N13O14P.ClH.Co.H2O/c1-29-20-39-40(21-30(29)2)75(28-70-39)57-52(84)53(41(27-76)87-57)89-90(85,86)88-31(3)26-69-49(83)18-19-59(8)37(22-46(66)80)56-62(11)61(10,25-48(68)82)36(14-17-45(65)79)51(74-62)33(5)55-60(9,24-47(67)81)34(12-15-43(63)77)38(71-55)23-42-58(6,7)35(13-16-44(64)78)50(72-42)32(4)54(59)73-56;;;/h20-21,23,28,31,34-37,41,52-53,56-57,76,84H,12-19,22,24-27H2,1-11H3,(H15,63,64,65,66,67,68,69,71,72,73,74,77,78,79,80,81,82,83,85,86);1H;;1H2/q;;+3;/p-3/t31-,34-,35-,36-,37+,41-,52-,53-,56?,57+,59-,60+,61+,62+;;;/m1.../s1
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | Co |
| Molecular Weight | 58.9332 |
| Charge | 3 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | HO |
| Molecular Weight | 17.0073 |
| Charge | -1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C62H88N13O14P |
| Molecular Weight | 1270.4146 |
| Charge | -2 |
| Count |
|
| Stereochemistry | EPIMERIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 13 / 14 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:15:47 UTC 2023
by
admin
on
Fri Dec 15 15:15:47 UTC 2023
|
| Record UNII |
B2B1VB7X21
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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Common Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Code System | Code | Type | Description | ||
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B2B1VB7X21
Created by
admin on Fri Dec 15 15:15:47 UTC 2023 , Edited by admin on Fri Dec 15 15:15:47 UTC 2023
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1947247
Created by
admin on Fri Dec 15 15:15:47 UTC 2023 , Edited by admin on Fri Dec 15 15:15:47 UTC 2023
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100000092184
Created by
admin on Fri Dec 15 15:15:47 UTC 2023 , Edited by admin on Fri Dec 15 15:15:47 UTC 2023
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1324319
Created by
admin on Fri Dec 15 15:15:47 UTC 2023 , Edited by admin on Fri Dec 15 15:15:47 UTC 2023
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121494087
Created by
admin on Fri Dec 15 15:15:47 UTC 2023 , Edited by admin on Fri Dec 15 15:15:47 UTC 2023
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59461-30-2
Created by
admin on Fri Dec 15 15:15:47 UTC 2023 , Edited by admin on Fri Dec 15 15:15:47 UTC 2023
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HYDROXOCOBALAMIN HYDROCHLORIDE
Created by
admin on Fri Dec 15 15:15:47 UTC 2023 , Edited by admin on Fri Dec 15 15:15:47 UTC 2023
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PRIMARY | Description: Dark red crystals or a red, crystalline powder; odourless. Solubility: Soluble in water. Category: Antianaemia drug. Storage: Hydroxocobalamin chloride or sulfate should be kept in a tightly closed container, protected from light, and stored at a temperature between 2? and 8?C. Labeling: The designation on the container should state whether the substance is the chloride or the sulfate salt. Additional information: Even in the absence of light, Hydroxocobalamin chloride and Hydroxocobalamin sulfate are gradually degraded on exposure to a humid atmosphere, the decomposition being faster at higher temperatures.Definition: Hydroxocobalamin chloride contains not less than 96.0% and not more than 102.0% of C62H90ClCoN13O15P, calculated with reference to the dried substance; Hydroxocobalamin sulfate contains not less than 96.0% and not more than 102.0% of C124H180Co2N26O34P2S, calculated with reference to the dried substance. | ||
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SUB12054MIG
Created by
admin on Fri Dec 15 15:15:47 UTC 2023 , Edited by admin on Fri Dec 15 15:15:47 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |