Shanghai Nianxing Industrial Co., Ltd
China
Product Name: Macamide B
Price:
Purity: 98.0%
Stocking Period: 10 Day
Contact: Yang

BioBioPha
China
Product Name: N-Benzylhexadecanamide
Price: ￥Inquiry/5mg
Purity: 95.0%
Stocking Period: 10 Day
Contact: Xueping-Zheng

Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: Hexadecanamide, N-(phenylmethyl)-
Price: $Inquiry/100g $Inquiry/1kg $Inquiry/100kg $Inquiry/1000kg
Purity: 98.0%
Stocking Period: Inquiry
Contact: Ms Wang

74058-71-2

74058-71-2 structure

Name: Macamide B
Chemical Name: N-benzylhexadecanamide
CAS Number: 74058-71-2
Molecular Formula: C₂₃H₃₉NO
Molecular Weight: 345.56200
Catalog: Natural product Alkaloid
Create Date: 2018-03-23 08:00:00
Modify Date: 2024-01-06 18:45:32
N-Benzylpalmitamide is a macamide isolated from Lepidium meyenii, acts as an inhibitor of fatty acid amide hydrolase (FAAH).

Name	N-benzylhexadecanamide
Synonyms	N-benzylpalmitamide N-Benzyl-palmitinamid N-benzyl-hexadecanamide N-hexadecanoyl benzylamine N-Benzyl-palmitamid N-benzylhexylhexadecanamide

Description	N-Benzylpalmitamide is a macamide isolated from Lepidium meyenii, acts as an inhibitor of fatty acid amide hydrolase (FAAH).
Related Catalog	Signaling Pathways >> Metabolic Enzyme/Protease >> FAAH Signaling Pathways >> Neuronal Signaling >> FAAH Natural Products >> Alkaloid Research Areas >> Others
Target	FAAH[1]
In Vitro	N-Benzylpalmitamide is an inhibitor of fatty acid amide hydrolase (FAAH), and shows 24.8% and 43.8% inhibition on FAAH at 10 μM and 500 μM, respectively[1].
References	[1]. Wu H, et al. Macamides and their synthetic analogs: evaluation of in vitro FAAH inhibition. Bioorg Med Chem. 2013 Sep 1;21(17):5188-97.

Melting Point	95-96℃
Molecular Formula	C₂₃H₃₉NO
Molecular Weight	345.56200
Exact Mass	345.30300
PSA	32.59000
LogP	7.62440

Hazard Codes	Xi

57-10-3

100-46-9

~89%

74058-71-2

Literature: Komura, Kenichi; Nakano, Yu; Koketsu, Mamoru Green Chemistry, 2011 , vol. 13, # 4 p. 828 - 831

544-63-8

100-46-9

~86%

74058-71-2

Literature: Wu, Hui; Kelley, Charles J.; Pino-Figueroa, Alejandro; Vu, Huyen D.; Maher, Timothy J. Bioorganic and Medicinal Chemistry, 2013 , vol. 21, # 17 p. 5188 - 5197

628-97-7

100-46-9

~88%

74058-71-2

Literature: Ranu, Brindaban C.; Dutta, Pinak Synthetic Communications, 2003 , vol. 33, # 2 p. 297 - 301

74058-64-3

100-46-9

~95%

74058-71-2

Literature: Nagao, Yoshimitsu; Seno, Kaoru; Kawabata, Kohji; Miyasaka, Tadayo; Takao, Sachiko; Fujita, Eiichi Tetrahedron Letters, 1980 , vol. 21, p. 841 - 844 Title/Abstract View citing articles Show Details Nagao, Yoshimitsu; Seno, Kaoru; Kawabata, Kohji; Miyasaka, Tadao; Takao, Sachiko; Fujita, Eiichi Chemical & Pharmaceutical Bulletin, 1984 , vol. 32, # 7 p. 2687 - 2699

555-44-2

100-46-9

~96%

74058-71-2

Literature: Feairheller, S. H.; Bistline, R. G.; Bilyk, A.; Dudley, R. L.; Kozempel, M. F.; Haas, M. J. Journal of the American Oil Chemists' Society, 1994 , vol. 71, # 8 p. 863 - 866

100663-86-3

100-46-9

~97%

74058-71-2

14178-31-5

Literature: Miyasaka, Tadayo; Noguchi, Shunsaku Chemistry Letters, 1985 , p. 701 - 704

57-10-3

74058-71-2

Literature: Nagao, Yoshimitsu; Seno, Kaoru; Kawabata, Kohji; Miyasaka, Tadayo; Takao, Sachiko; Fujita, Eiichi Tetrahedron Letters, 1980 , vol. 21, p. 841 - 844

112-67-4

74058-71-2

Literature: Miyasaka, Tadayo; Noguchi, Shunsaku Chemistry Letters, 1985 , p. 701 - 704

100-46-9

112-67-4

74058-71-2

Literature: Bowen; Smith Journal of the American Chemical Society, 1940 , vol. 62, p. 3522

Precursor 8
57-10-3 100-46-9 544-63-8 628-97-7
74058-64-3 555-44-2 100663-86-3 112-67-4
DownStream 0

74058-71-2	105708-64-3
125524-71-2	119509-26-1
145458-92-0	105650-11-1
132938-12-6	2552-06-9
588675-30-3	111278-00-3
2413869-20-0	1158522-08-7
940364-43-2	2114399-60-7
2357770-60-4	134104-43-1
131615-57-1	6906-52-1
2443867-36-3	930439-75-1