74875-70-0
Chemical Structure
3-Hydroxyhexanoyl-CoA
Synonym(s): 3-Hydroxyhexanoyl-coenzyme A; [R,S]-Lactyl-CoA
- CAS No.: 74875-70-0
- Formula:C27H46N7O18P3S
- Molecular Weight:881.68
InChIKey: VAAHKRMGOFIORX-SNIDVWGTSA-N
SMILES: CC([C@H](C(NCCC(NCCSC(CC(O)CCC)=O)=O)=O)O)(C)COP(OP(OC[C@H]1O[C@@H](N2C3=NC=NC(N)=C3N=C2)[C@H](O)[C@@H]1OP(O)(O)=O)(O)=O)(O)=O
Biological Activity: 3-Hydroxyhexanoyl-CoA (3-Hydroxyhexanoyl-coenzyme A) is a derivative of coenzyme A, which is produced from hexanoic acid via β-oxidation[1][2][3][4][5].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
3-Hydroxyhexanoyl-CoA | 95.66% | 3-Hydroxyhexanoyl-CoA (3-Hydroxyhexanoyl-coenzyme A) is a derivative of coenzyme A, which is produced from hexanoic acid via β-oxidation. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
- [1]. Wang H, et al. Production of PHA copolymers consisting of 3‑hydroxybutyrate and 3‑hydroxyhexanoate (PHBHHx) by recombinant Halomonas bluephagenesis. Chemical Engineering Journal. 2023;466:143261.
- [2]. Jeon JM, et al. Biosynthesis of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (P(HB-co-HHx)) from butyrate using engineered Ralstonia eutropha. Applied microbiology and biotechnology. 2014 Jun;98(12):5461-9.
- [3]. Lim G, et al. Discovery of a High 3-Hydroxyhexanoate Containing Poly-3-hydroxybutyrate-co-3-hydroxyhexanoate Producer-, Cupriavidus sp. Oh_1 with Enhanced Fatty Acid Metabolism. Polymers (Basel). 2025 Jun 30;17(13):1824.
- [4]. PubChem Compound Summary for CID 146674183, 3‑hydroxyhexanoyl‑SCoA [Internet]. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information; 2020 Jul 13 [cited 2026 Aug 17].
- [5]. PubChem Compound Summary for CID 440609, S‑{1‑[(2R,3S,4R,5R)‑5‑(6‑Amino‑9H‑purin‑9‑yl)‑4‑hydroxy‑3‑(phosphonooxy)oxolan‑2‑yl]‑3,5,9‑trihydroxy‑8,8‑dimethyl‑3,5,10,14‑tetraoxo‑2,4,6‑trioxa‑11,15‑diaza‑3λ~5~,5λ~5~‑diphosphaheptadecan‑17‑yl} (3S)‑3‑hydroxyhexanethioate [Internet]. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information; 2004 Sep 16 [cited 2026 Aug 17].
Keywords