Valinomycin
≥99.0% (TLC)
Manufacturer: Sigma Aldrich
CAS Number: 2001-95-8
Synonym(S): Cyclo(L-Val-D-HyIva-D-Val-L-Lac-)3: HyIva = α-Hydroxyisovaleric acid, Lac = Lactic acid
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 10 MG | 94675-10-MG | In Stock | ₹ 11,322.95 |
| 100 MG | 94675-100-MG | In Stock | ₹ 58,195.20 |
| 500 MG | 94675-500-MG | In Stock | ₹ 1,86,114.23 |
94675 - 10 MG
In Stock
Quantity
1
Base Price: ₹ 11,322.95
GST (18%): ₹ 2,038.131
Total Price: ₹ 13,361.081
Quality Level
200
Assay
≥99.0% (TLC)
form
powder
mp
187-190 °C
antibiotic activity spectrum
mycobacteria
Mode of action
cell membrane | interferes
storage temp.
2-8°C
SMILES string
CC(C)[C@@H]1NC(=O)[C@H](C)OC(=O)[C@@H](NC(=O)[C@H](OC(=O)[C@@H](NC(=O)[C@H](C)OC(=O)[C@H](NC(=O)[C@H](OC(=O)[C@@H](NC(=O)[C@H](C)OC(=O)[C@H](NC(=O)[C@H](OC1=O)C(C)C)C(C)C)C(C)C)C(C)C)C(C)C)C(C)C)C(C)C)C(C)C
InChI
1S/C54H90N6O18/c1-22(2)34-49(67)73-31(19)43(61)55-38(26(9)10)53(71)77-41(29(15)16)47(65)59-36(24(5)6)51(69)75-33(21)45(63)57-39(27(11)12)54(72)78-42(30(17)18)48(66)60-35(23(3)4)50(68)74-32(20)44(62)56-37(25(7)8)52(70)76-40(28(13)14)46(64)58-34/h22-42H,1-21H3,(H,55,61)(H,56,62)(H,57,63)(H,58,64)(H,59,65)(H,60,66)/t31-,32-,33-,34-,35+,36+,37-,38-,39-,40+,41+,42+/m0/s1
InChI key
FCFNRCROJUBPLU-RPUZOQEISA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Potassium ionophore I | Supelco | ₹ 64,148.95 | |
| | Valinomycin | Sigma Aldrich | ₹ 10,543.55 - ₹ 2,22,302.20 | |
| | Valinomycin | Sigma Aldrich | ₹ 9,948.18 |
Related Products
Description
- General description: Chemical structure: peptide
- Application: Valinomycin has been used as an internal standard in the cytotoxicity assay for the detection of cereulide produced by emetic Bacillus cereus.[4] It has also been used in the measurement of the electrogenicity of bile salt/H+ antiport in Escherichia coli.[5]
- Biochem/physiol Actions: K+-selective ionophoric cyclodepsipeptide; potassium ionophore which uncouples oxidative phosphorylation, induces apoptosis in murine thymocytes, inhibits NGF-induced neuronal differentiation and antagonizes ET-induced vasoconstriction.
- Other Notes: Review[7]
SAFETY INFORMATION
Pictograms
Signal Word
Danger
Hazard Statements
Precautionary Statements
P262 - P264 - P280 - P301 + P310 - P302 + P352 + P310 - P361 + P364
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 1 Oral
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
Quality Level: 200
Assay: ≥99.0% (TLC)
form: powder
mp: 187-190 °C
antibiotic activity spectrum: mycobacteria
Mode of action: cell membrane | interferes
storage temp.: 2-8°C
SMILES string: CC(C)[C@@H]1NC(=O)[C@H](C)OC(=O)[C@@H](NC(=O)[C@H](OC(=O)[C@@H](NC(=O)[C@H](C)OC(=O)[C@H](NC(=O)[C@H](OC(=O)[C@@H](NC(=O)[C@H](C)OC(=O)[C@H](NC(=O)[C@H](OC1=O)C(C)C)C(C)C)C(C)C)C(C)C)C(C)C)C(C)C)C(C)C)C(C)C
InChI: 1S/C54H90N6O18/c1-22(2)34-49(67)73-31(19)43(61)55-38(26(9)10)53(71)77-41(29(15)16)47(65)59-36(24(5)6)51(69)75-33(21)45(63)57-39(27(11)12)54(72)78-42(30(17)18)48(66)60-35(23(3)4)50(68)74-32(20)44(62)56-37(25(7)8)52(70)76-40(28(13)14)46(64)58-34/h22-42H,1-21H3,(H,55,61)(H,56,62)(H,57,63)(H,58,64)(H,59,65)(H,60,66)/t31-,32-,33-,34-,35+,36+,37-,38-,39-,40+,41+,42+/m0/s1
InChI key: FCFNRCROJUBPLU-RPUZOQEISA-N
Quality Level: 300
Assay: __
form: __
mp: 153-159 °C (lit.)
antibiotic activity spectrum: __
Mode of action: __
storage temp.: __
SMILES string: __
InChI: __
InChI key: __
Quality Level: 300
Assay: __
form: powder
mp: 107-109 °C (lit.)
antibiotic activity spectrum: __
Mode of action: __
storage temp.: __
SMILES string: COC(=O)c1cc(cc(c1)[N+]([O-])=O)[N+]([O-])=O
InChI: 1S/C8H6N2O6/c1-16-8(11)5-2-6(9(12)13)4-7(3-5)10(14)15/h2-4H,1H3
InChI key: __
