Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H6O10S2.2Na |
Molecular Weight | 396.258 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[Na+].CC1=CC(=O)OC2=C1C=C(OS([O-])(=O)=O)C(OS([O-])(=O)=O)=C2
InChI
InChIKey=YCZIKIZDMUKKPA-UHFFFAOYSA-L
InChI=1S/C10H8O10S2.2Na/c1-5-2-10(11)18-7-4-9(20-22(15,16)17)8(3-6(5)7)19-21(12,13)14;;/h2-4H,1H3,(H,12,13,14)(H,15,16,17);;/q;2*+1/p-2
Molecular Formula | C10H6O10S2 |
Molecular Weight | 350.279 |
Charge | -2 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Sulmarin is a water-soluble coumarin derivative with vitamin P activity. In preclinical models Sulmarin facilitates excitatory transmission from parasympathetic fibers to the gastric musculature, increasing acetylcholine release. Sulmarin reduced the tone of isolated calf coronary arteries and also inhibited the contractile response of the arteries to angiotensin II amide (Hypertensin).
Originator
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:05:27 GMT 2023
by
admin
on
Fri Dec 15 19:05:27 GMT 2023
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Record UNII |
719219P18R
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Record Status |
Validated (UNII)
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Record Version |
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-
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DTXSID60146211
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719219P18R
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13962
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100000085071
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1040-23-9
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SUB04642MIG
Created by
admin on Fri Dec 15 19:05:27 GMT 2023 , Edited by admin on Fri Dec 15 19:05:27 GMT 2023
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |