
Aristolochic acid D
CAS No. 17413-38-6
Aristolochic acid D( —— )
Catalog No. M23786 CAS No. 17413-38-6
Aristolochic acid D is an aristolochic acid derivative isolated from stems of Aristolochia indica. Aristolochic acid is nephrotoxin and carcinogen.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 288 | In Stock |
![]() ![]() |
10MG | 529 | In Stock |
![]() ![]() |
25MG | 863 | In Stock |
![]() ![]() |
50MG | 1152 | In Stock |
![]() ![]() |
100MG | Get Quote | In Stock |
![]() ![]() |
200MG | Get Quote | In Stock |
![]() ![]() |
500MG | Get Quote | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameAristolochic acid D
-
NoteResearch use only, not for human use.
-
Brief DescriptionAristolochic acid D is an aristolochic acid derivative isolated from stems of Aristolochia indica. Aristolochic acid is nephrotoxin and carcinogen.
-
DescriptionAristolochic acid D is an aristolochic acid derivative isolated from stems of Aristolochia indica. Aristolochic acid is nephrotoxin and carcinogen.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number17413-38-6
-
Formula Weight357.27
-
Molecular FormulaC17H11NO8
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 25 mg/mL (69.98 mM)
-
SMILESO=C(C1=C2C([N+]([O-])=O)=CC3=C(OC)C=C(O)C=C3C2=C(OCO4)C4=C1)O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog



related products
-
Substance P
Substance P (SP) is an undecapeptide (a peptide composed of a chain of 11 amino acid residues) member of the tachykinin neuropeptide family.
-
C-Reactive Protein (...
C-Reactive Protein (CRP) 201-206 is the 201-206 fragment of C-Reactive Protein.?C-Reactive Protein (CRP), the prototypic marker of inflammation, is a cardiovascular risk marker and may promote atherogenesis.
-
Denosumab
Denosumab is a monoclonal antibody given subcutaneously that inhibits osteoclast activity by targeting the RANK ligand.