ChemicalBook > CAS DataBase List > (±)16-HETE

(±)16-HETE

Product Name
(±)16-HETE
CAS No.
128914-46-5
Chemical Name
(±)16-HETE
Synonyms
(±)16-HETE;JEKNPVYFNMZRJG-UFINWASNSA-N;16-hydroxy-5(Z),8(Z),11(Z),14(Z)-eicosatetraenoic acid;5,8,11,14-Eicosatetraenoic acid, 16-hydroxy-, (5Z,8Z,11Z,14Z)-
CBNumber
CB02589794
Molecular Formula
C20H32O3
Formula Weight
320.47
MOL File
128914-46-5.mol
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(±)16-HETE Property

storage temp. 
Store at -20°C
solubility 
0.1 M Na2CO3: 2 mg/ml; DMF: Miscible; DMSO: Miscible; Ethanol: Miscible; PBS (pH 7.2): 0.8 mg/ml
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
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N-Bromosuccinimide Price

Cayman Chemical
Product number
10010635
Product name
(±)16-HETE
Purity
≥98%
Packaging
25μg
Price
$146
Updated
2024/03/01
Cayman Chemical
Product number
10010635
Product name
(±)16-HETE
Purity
≥98%
Packaging
50μg
Price
$278
Updated
2024/03/01
Cayman Chemical
Product number
10010635
Product name
(±)16-HETE
Purity
≥98%
Packaging
100μg
Price
$525
Updated
2024/03/01
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(±)16-HETE Chemical Properties,Usage,Production

Description

Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. (±)16-HETE is the racemic version of a minor CYP450 metabolite of arachidonic acid released by the kidney upon angiotensin II stimulation. The biological activity of 16-HETE is stereospecific. 16(R)-HETE dose-dependently stimulates vasodilation of the rabbit kidney, however 16(S)-HETE does not affect perfusion pressure. At a concentration of 2 μM the (S)-enantiomer of 16-HETE inhibits proximal tubule ATPase activity by as much as 60%, whereas the (R)-isomer has negligible effects on ATPase activity.

Definition

ChEBI: A HETE that consists of arachidonic acid bearing an additional hydroxy substituent at position 16.

(±)16-HETE Preparation Products And Raw materials

Raw materials

Preparation Products

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(±)16-HETE Suppliers

Yichang Zhongyitai Trading Co., Ltd.
Tel
0717-6449896 13886658719
Fax
0717-6558598
Email
root@zhongyitai.com
Country
China
ProdList
1977
Advantage
58
Alfa Chemistry
Tel
1-516-6625404
Fax
1-516-927-0118
Email
support@alfa-chemistry.com
Country
United States
ProdList
9171
Advantage
60
Shanghai Hongye Biotechnology Co. Ltd
Tel
400-9205774
Email
sales@glpbio.cn
Country
China
ProdList
6870
Advantage
58
Alfa Chemistry
Tel
+1-5166625404
Fax
1-516-927-0118
Email
Info@alfa-chemistry.com
Country
United States
ProdList
21317
Advantage
58
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11289
Advantage
58
MedBioPharmaceutical Technology Inc
Tel
021-69568360 18916172912
Email
order@med-bio.cn
Country
China
ProdList
8141
Advantage
58
amyjetsci
Tel
027-59626688 18771149750
Email
sales@amyjet.com
Country
China
ProdList
3004
Advantage
58
Shanghai Yifei Biotechnology Co. , Ltd.
Tel
021-65675885 18964387627
Email
customer_service@efebio.com
Country
China
ProdList
8740
Advantage
58
Shanghai Aladdin Biochemical Technology Co.,Ltd.
Tel
+86-18521732826
Email
market@aladdin-e.com
Country
China
ProdList
48467
Advantage
58
TargetMol Chemicals Inc.
Tel
15002134094
Email
marketing@targetmol.com
Country
China
ProdList
24246
Advantage
58

128914-46-5, (±)16-HETERelated Search:


  • (±)16-HETE
  • JEKNPVYFNMZRJG-UFINWASNSA-N
  • 5,8,11,14-Eicosatetraenoic acid, 16-hydroxy-, (5Z,8Z,11Z,14Z)-
  • 16-hydroxy-5(Z),8(Z),11(Z),14(Z)-eicosatetraenoic acid
  • 128914-46-5