Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C35H60N2O4 |
Molecular Weight | 572.8619 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 10 / 10 |
E/Z Centers | 0 |
Charge | 2 |
SHOW SMILES / InChI
SMILES
[H][C@@]12C[C@@H]([C@H](OC(C)=O)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CC[C@@]4([H])C[C@H](OC(C)=O)[C@H](C[C@]34C)[N+]5(C)CCCCC5)[N+]6(C)CCCCC6
InChI
InChIKey=GVEAYVLWDAFXET-XGHATYIMSA-N
InChI=1S/C35H60N2O4/c1-24(38)40-32-21-26-13-14-27-28(35(26,4)23-31(32)37(6)19-11-8-12-20-37)15-16-34(3)29(27)22-30(33(34)41-25(2)39)36(5)17-9-7-10-18-36/h26-33H,7-23H2,1-6H3/q+2/t26-,27+,28-,29-,30-,31-,32-,33-,34-,35-/m0/s1
Molecular Formula | C35H60N2O4 |
Molecular Weight | 572.8619 |
Charge | 2 |
Count |
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Stereochemistry | MIXED |
Additional Stereochemistry | No |
Defined Stereocenters | 10 / 10 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:28:14 UTC 2023
by
admin
on
Fri Dec 15 15:28:14 UTC 2023
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Record UNII |
J76UF062FS
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Record Status |
Validated (UNII)
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Record Version |
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-
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Name | Type | Language | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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WHO-VATC |
QM03AC01
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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WHO-ATC |
M03AC01
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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NDF-RT |
N0000175720
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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NCI_THESAURUS |
C29696
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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NDF-RT |
N0000175732
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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Code System | Code | Type | Description | ||
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SUB03618MIG
Created by
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PRIMARY | |||
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7907
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PRIMARY | |||
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DTXSID7048405
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PRIMARY | |||
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100000085535
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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C61876
Created by
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PRIMARY | |||
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4001
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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Pancuronium
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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16974-53-1
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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DB01337
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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J76UF062FS
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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2052
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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J76UF062FS
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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441289
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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Pancuronium
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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D010197
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | |||
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7883
Created by
admin on Fri Dec 15 15:28:14 UTC 2023 , Edited by admin on Fri Dec 15 15:28:14 UTC 2023
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PRIMARY | RxNorm |
Related Record | Type | Details | ||
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BINDER->LIGAND |
BINDING
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Related Record | Type | Details | ||
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METABOLITE LESS ACTIVE -> PARENT |
In bile too; Pancuronium is 50 times more potent than this metabolite
PLASMA; URINE
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METABOLITE LESS ACTIVE -> PARENT |
In bile too; Pancuronium is 2 times more potent than this metabolite
PLASMA; URINE
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METABOLITE LESS ACTIVE -> PARENT |
In bile too; Pancuronium is 54 times more potent than this metabolite
PLASMA; URINE
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Related Record | Type | Details | ||
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PARENT -> IMPURITY |
any spot due to impurity B is not more intense than the spot in the chromatogram obtained with reference solution (b)
CHROMATOGRAPHIC PURITY (TLC)
EP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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Biological Half-life | PHARMACOKINETIC |
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