HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954186Generated: November 2, 2026
Potassium Chloride → HCID 178508912, compound
https://huagongshe.com/reaction/1954186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Chloride | HCID 4873 | — |
| Reactant | 5'-Atp | HCID 5957 | — |
| Reactant | Triethanolamine | HCID 7618 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Reactant | HCID 131722006 | HCID 131722006 | — |
| Reactant | HCID 137182957 | HCID 137182957 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178508912 | HCID 178508912 | — |
Reaction Steps
10-formyltetrahydrofolate-synthetase catalyzes the reaction, formate+THF+ATP→10-formyl-THF+ADP+Pi. A test tube containing 100 μL 1 M triethanolamine buffer (pH 7.5), 100 μL 1 M ammonium formate (pH 7.5), 100 μL 25 mM MgCl2, 100 μL 2 M KCl, 100 μL 10 mM THF, freshly made 100 μL 20 mM ATP, and 390 μL water was pre-incubated for 2 min at 30° C. A 10 μL aliquot of the extracted sample containing enzyme was added and incubated 15 min at 30° C. The reaction was terminated by adding 2 mL 0.36 N HCl. The 10-formyl-THF formed during the incubation period was converted to 5,10-methenyl-THF by the acid. The absorbency was measured at 350 nm against a water blank and the 5,10-methenyl-THF formed was determined by using an extinction coefficient of 24,900 M-1 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06121195 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-a6c17b6d46424c62a42bf7ac1568f471 |
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| Source note | uspto-grants-2000_09 |
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