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OLEYLHYDROXAMIC ACID

Product Name
OLEYLHYDROXAMIC ACID
CAS No.
10335-69-0
Chemical Name
OLEYLHYDROXAMIC ACID
Synonyms
Einecs 233-728-4;N-hydroxyoleamide;N-Hydroxyoleylamide;N-Hydroxyoleic amide;OLEYLHYDROXAMIC ACID;Oleoylhydroxamic acid;N-Hydroxy-9-octadecenamide;(Z)-N-Hydroxy-9-octadecenamide;(9Z)-9-Octadecenehydroxamic acid;9-Octadecenamide, N-hydroxy-, (9Z)-
CBNumber
CB9421385
Molecular Formula
C18H35NO2
Formula Weight
297.48
MOL File
10335-69-0.mol
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OLEYLHYDROXAMIC ACID Property

Melting point:
61 °C
Density 
0.921±0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
≤50mg/ml in ethanol;50mg/ml in DMSO;50mg/ml in dimethyl formamide
form 
crystalline solid
pka
9.48±0.20(Predicted)
color 
White to off-white
InChI
1S/C18H35NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(20)19-21/h9-10,21H,2-8,11-17H2,1H3,(H,19,20)/b10-9-
InChIKey
LTXHELLMCCEDJG-KTKRTIGZSA-N
SMILES
N(O)C(=O)CCCCCCC\C=C/CCCCCCCC
EPA Substance Registry System
N-Hydroxyoleylamide (10335-69-0)
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Safety

WGK Germany 
WGK 1
TSCA 
TSCA listed
Storage Class
11 - Combustible Solids
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

H413May cause long lasting harmful effects to aquatic life

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P321Specific treatment (see … on this label).

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
444244
Product name
MMP-2 Inhibitor I
Purity
The MMP-2 Inhibitor I, also referenced under CAS 10335-69-0, controls the biological activity of MMP-2. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.
Packaging
10mg
Price
$130
Updated
2026/03/19
Cayman Chemical
Product number
19644
Product name
MMP-2 Inhibitor I
Purity
≥98%
Packaging
5mg
Price
$65
Updated
2024/03/01
Cayman Chemical
Product number
19644
Product name
MMP-2 Inhibitor I
Purity
≥98%
Packaging
10mg
Price
$96
Updated
2024/03/01
ApexBio Technology
Product number
C5615
Product name
MMP-2InhibitorI
Packaging
10mg
Price
$108
Updated
2021/12/16
ApexBio Technology
Product number
C5615
Product name
MMP-2InhibitorI
Packaging
5mg
Price
$71
Updated
2021/12/16
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OLEYLHYDROXAMIC ACID Chemical Properties,Usage,Production

Uses

MMP-2 Inhibitor I (OA-Hy) is a potent MMP-2 inhibitor with a Ki of 1.7 μM[1].

Biological Activity

mmp-2 inhibitor i, a hydroxamate-based, long-chain fatty acid, is a reversible inhibitor of matrix metalloproteinase (mmp)-2.matrix metalloproteinases (mmps) have been involved in the degradation of extracellular matrix. mmps contribute to long-term remodeling processes such as embryogenesis, tumor invasion, inflammation, angiogenesis, and wound healing. mmp-2, also known as gelatinase a or type iv collagenase, has been involved in regulating diverse cellular functions independent of its action on the extracellular matrix, including vascular tone, platelet aggregation, and mediation of the acute mechanical dysfunction of the heart immediately after ischemia and reperfusion [2]. up-regulation of mmp-2 has been associated with tumor invasion and metastasis [3].mmp-2 inhibitor i inhibited the activity of matrix metalloproteinase (mmp)-2 with the ki value of 1.6 μm [1]. mmp-2 inhibitor i attenuated cancer cell migration [3]. mmp-2 inhibitor i had also been used to preserve blood-brain barrier function in a wistar rat model of pneumococcal meningitis [4].

IC 50

MMP-2: 1.7 μM (Ki)

References

[1] berton a, rigot v, huet e, et al. involvement of fibronectin type ii repeats in the efficient inhibition of gelatinases a and b by long-chain unsaturated fatty acids[j]. journal of biological chemistry, 2001, 276(23): 20458-20465.
[2] wang w, schulze c j, suarez-pinzon w l, et al. intracellular action of matrix metalloproteinase-2 accounts for acute myocardial ischemia and reperfusion injury[j]. circulation, 2002, 106(12): 1543-1549.
[3] emmert-buck m r, roth m j, zhuang z, et al. increased gelatinase a (mmp-2) and cathepsin b activity in invasive tumor regions of human colon cancer samples[j]. the american journal of pathology, 1994, 145(6): 1285.
[4] barichello t, generoso j s, michelon c m, et al. inhibition of matrix metalloproteinases-2 and-9 prevents cognitive impairment induced by pneumococcal meningitis in wistar rats[j]. experimental biology and medicine, 2014, 239(2): 225-231.

OLEYLHYDROXAMIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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OLEYLHYDROXAMIC ACID Suppliers

SHANGHAI FORTUNE CHEMICAL TECHNOLOGY CO., LTD
Tel
13816107857
Fax
qq: 276312098
Email
sales@fortunechem-sh.com
Country
China
ProdList
984
Advantage
58
Changzhou Chenhong Biotechnology Co., Ltd.
Tel
+86-0519-85788828 +86-13775037613
Email
sales@chemrenpharm.com
Country
China
ProdList
4032
Advantage
58
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11218
Advantage
58
MedBioPharmaceutical Technology Inc
Tel
021-69568360 18916172912
Email
order@med-bio.cn
Country
China
ProdList
8140
Advantage
58
Tianmen Hengchang Chemical Co., Ltd
Tel
027-59322316 15172518801
Fax
027-59322316
Email
1018286633@qq.com
Country
China
ProdList
9531
Advantage
58
Hubei Qifei Pharmaceutical Chemical Co., Ltd
Tel
027-59322506 18071128681
Fax
027-59322506
Email
1438082200@qq.com
Country
China
ProdList
9601
Advantage
58
Shaanxi Dideu Newmaterial Co., Ltd.
Tel
029-029-63373950 17392216152
Email
1050@dideu.com
Country
China
ProdList
9998
Advantage
58
Shanghai Yifei Biotechnology Co. , Ltd.
Tel
021-65675885 18964387627
Email
customer_service@efebio.com
Country
China
ProdList
11972
Advantage
58
Cayman Chemical Company
Tel
800-364-9897
Email
sales@caymanchem.com
Country
China
ProdList
6838
Advantage
58
Merck KGaA
Tel
21-20338288
Email
ordercn@merckgroup.com
Country
China
ProdList
6038
Advantage
58

10335-69-0, OLEYLHYDROXAMIC ACIDRelated Search:


  • OLEYLHYDROXAMIC ACID
  • N-hydroxyoleamide
  • (9Z)-9-Octadecenehydroxamic acid
  • (Z)-N-Hydroxy-9-octadecenamide
  • Hydroxamate derivative of oleic acid
  • N-Hydroxyoleic amide
  • Oleoylhydroxamic acid
  • 9-Octadecenamide, N-hydroxy-, (9Z)-
  • Einecs 233-728-4
  • N-Hydroxy-9-octadecenamide
  • N-Hydroxyoleylamide
  • 10335-69-0