Fatty acid conjugates
Positional and geometric isomers of fatty acids with conjugated double bonds; implies four consecutive unsaturated links, and results in a delocalization of electrons along the double-bonded carbons; available in carbon chains of varying length.
Quantity
- (1)
- (1)
- (14)
- (184)
- (31)
- (2)
- (10)
- (1)
- (46)
- (6)
- (4)
- (14)
- (3)
- (1)
- (127)
- (20)
- (37)
- (11)
- (3)
- (1)
- (8)
- (1)
- (1)
- (2)
- (2)
- (5)
- (2)
- (1)
- (2)
- (3)
- (22)
- (1)
- (4)
- (2)
- (1)
- (2)
- (6)
- (2)
- (266)
- (5)
- (35)
- (11)
- (54)
- (5)
- (25)
- (10)
- (3)
- (2)
- (3)
- (3)
- (3)
- (261)
- (16)
- (19)
- (6)
- (1)
- (32)
- (6)
- (14)
- (121)
- (28)
- (12)
- (7)
- (1)
- (1)
- (1)
Molecular Weight (g/mol)
- (2)
- (8)
- (22)
- (2)
- (1)
- (2)
- (3)
- (1)
- (2)
- (7)
- (27)
- (1)
- (1)
- (7)
- (1)
- (8)
- (10)
- (18)
- (2)
- (20)
- (22)
- (3)
- (2)
- (8)
- (4)
- (1)
- (2)
- (9)
- (4)
- (2)
- (1)
- (1)
- (1)
- (6)
- (1)
- (5)
- (6)
- (1)
- (4)
- (7)
- (7)
- (3)
- (2)
- (1)
- (5)
- (10)
- (4)
- (12)
- (5)
- (8)
- (2)
- (2)
- (2)
- (2)
- (2)
- (5)
- (2)
- (2)
- (1)
- (4)
- (6)
- (2)
- (1)
- (1)
- (1)
- (1)
- (5)
- (5)
- (2)
- (18)
- (5)
- (18)
- (2)
- (5)
- (1)
- (3)
- (3)
- (7)
- (6)
- (2)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (2)
- (1)
- (3)
- (9)
- (3)
- (2)
- (10)
- (6)
- (1)
- (4)
- (1)
- (5)
- (2)
- (18)
- (5)
- (4)
- (1)
- (5)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (3)
- (7)
- (14)
- (1)
- (2)
- (6)
- (2)
- (5)
- (2)
- (2)
- (6)
- (2)
- (2)
- (1)
- (4)
- (13)
- (1)
- (2)
- (1)
- (1)
- (9)
- (8)
- (1)
- (3)
- (4)
- (6)
- (2)
- (1)
- (1)
- (2)
- (5)
- (9)
- (3)
- (3)
- (4)
- (5)
- (3)
- (6)
- (2)
- (4)
- (2)
- (1)
- (2)
- (2)
- (4)
- (3)
- (9)
- (3)
- (3)
- (1)
- (6)
- (1)
- (1)
- (5)
- (11)
- (3)
- (2)
- (15)
- (3)
- (1)
- (3)
- (5)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (4)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (3)
- (1)
- (2)
- (2)
- (2)
- (5)
- (2)
- (4)
- (3)
- (3)
- (1)
- (1)
- (6)
- (7)
- (1)
- (1)
- (1)
- (9)
- (3)
- (6)
- (4)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (4)
- (2)
- (3)
- (6)
- (4)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (2)
- (4)
- (1)
- (2)
- (4)
- (9)
- (2)
- (1)
- (1)
- (1)
- (4)
- (23)
- (4)
- (1)
- (2)
- (4)
- (4)
- (1)
- (2)
- (2)
- (1)
- (1)
- (3)
- (9)
- (4)
- (1)
- (3)
- (8)
- (4)
- (3)
- (1)
- (4)
- (1)
- (7)
- (2)
- (2)
- (3)
- (2)
- (4)
- (5)
- (2)
- (9)
- (12)
- (3)
- (3)
- (2)
- (5)
- (26)
- (28)
- (4)
- (2)
- (4)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
- (1)
- (2)
- (6)
- (2)
- (2)
- (1)
- (22)
- (8)
- (2)
- (2)
- (1)
- (3)
- (1)
- (4)
- (3)
- (3)
- (9)
- (3)
- (1)
- (1)
- (2)
- (1)
- (1)
- (4)
- (8)
- (3)
- (1)
- (3)
- (7)
- (3)
- (2)
- (2)
- (5)
- (3)
- (2)
- (4)
- (4)
- (2)
- (1)
- (1)
- (5)
- (2)
- (10)
- (2)
- (6)
- (1)
- (1)
- (3)
- (5)
- (2)
- (2)
- (3)
- (4)
- (1)
- (2)
- (1)
- (1)
- (3)
- (3)
- (2)
- (1)
- (2)
- (5)
- (1)
- (6)
- (1)
- (2)
- (2)
- (2)
- (3)
- (2)
- (2)
- (6)
- (4)
- (10)
- (2)
- (2)
- (7)
- (3)
- (1)
- (1)
- (2)
- (5)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (1)
- (2)
- (4)
- (2)
- (2)
- (2)
- (1)
- (1)
- (3)
- (3)
- (3)
- (1)
- (3)
- (2)
- (3)
- (5)
- (3)
- (3)
- (1)
- (1)
- (1)
- (2)
- (2)
- (10)
- (1)
- (13)
- (1)
- (2)
- (1)
- (1)
- (1)
- (2)
- (4)
- (3)
Percent Purity
- (2)
- (1)
- (8)
- (8)
- (2)
- (2)
- (4)
- (1)
- (15)
- (2)
- (2)
- (2)
- (1)
- (1)
- (2)
- (14)
- (13)
- (24)
- (2)
- (4)
- (11)
- (3)
- (4)
- (39)
- (2)
- (30)
- (1)
- (39)
- (25)
- (126)
- (2)
- (2)
- (28)
- (2)
- (92)
- (4)
- (4)
- (17)
- (3)
- (6)
- (1)
- (10)
- (2)
- (25)
- (1)
- (13)
- (1)
- (3)
- (4)
- (3)
- (1)
- (5)
- (8)
- (3)
- (1)
- (3)
- (3)
- (4)
- (2)
- (2)
- (1)
- (3)
- (9)
- (8)
- (3)
- (75)
- (3)
- (2)
- (1)
- (27)
- (4)
- (6)
- (133)
- (6)
- (1)
- (198)
- (2)
- (2)
- (8)
- (4)
- (133)
- (17)
- (9)
- (3)
- (2)
- (2)
- (1)
Physical Form
- (9)
- (3)
- (3)
- (4)
- (3)
- (27)
- (3)
- (367)
- (3)
- (8)
- (7)
- (64)
- (2)
- (5)
- (12)
- (7)
- (3)
- (2)
- (4)
- (1)
- (3)
- (3)
- (4)
- (285)
- (2)
- (6)
- (3)
- (2)
- (6)
- (2)
- (3)
- (3)
- (101)
- (2)
- (5)
- (4)
- (2)
- (1)
- (4)
- (1)
- (6)
- (5)
- (24)
- (1)
- (20)
- (1)
Boiling Point
- (1)
- (1)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (6)
- (3)
- (2)
- (1)
- (3)
- (3)
- (3)
- (4)
- (2)
- (6)
- (2)
- (3)
- (3)
- (3)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (4)
- (2)
- (2)
- (3)
- (2)
- (1)
- (1)
- (2)
- (3)
- (3)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (5)
- (6)
- (2)
- (2)
- (2)
- (2)
- (4)
- (2)
- (2)
- (6)
- (2)
- (3)
- (3)
- (4)
- (3)
- (2)
- (2)
- (6)
- (3)
- (3)
- (2)
- (2)
- (2)
- (2)
- (3)
- (3)
- (3)
- (2)
- (1)
- (1)
- (1)
- (3)
- (2)
- (2)
- (6)
- (3)
- (2)
- (4)
- (1)
- (6)
- (1)
- (1)
- (2)
- (1)
- (5)
- (3)
- (2)
- (2)
- (3)
- (2)
- (3)
- (2)
- (2)
- (2)
- (1)
- (2)
- (2)
- (3)
- (3)
- (1)
- (4)
- (1)
- (3)
- (3)
- (2)
- (4)
- (5)
- (2)
- (2)
- (5)
- (2)
- (1)
- (2)
- (1)
- (4)
- (2)
- (1)
- (3)
- (2)
- (3)
- (3)
- (4)
- (1)
- (4)
- (1)
- (3)
- (3)
- (2)
- (2)
- (2)
- (3)
- (2)
- (3)
- (5)
- (2)
- (8)
- (4)
- (5)
- (4)
- (2)
- (5)
- (5)
- (3)
- (3)
- (1)
- (5)
- (2)
- (3)
- (1)
- (1)
- (4)
- (2)
- (2)
- (3)
- (4)
- (3)
- (4)
- (4)
- (3)
- (5)
- (4)
- (2)
- (3)
- (3)
- (2)
- (2)
- (2)
- (4)
- (4)
- (3)
- (1)
- (2)
- (6)
- (1)
- (2)
- (2)
- (3)
- (6)
- (3)
- (2)
- (1)
- (2)
- (3)
- (2)
- (3)
- (4)
- (3)
- (5)
- (4)
- (2)
- (1)
- (2)
- (2)
- (5)
- (4)
- (1)
- (2)
- (4)
- (2)
- (2)
- (3)
- (2)
- (5)
- (4)
- (2)
- (1)
- (5)
- (3)
- (4)
- (3)
- (8)
- (8)
- (4)
- (3)
- (9)
- (3)
- (5)
- (3)
- (3)
- (2)
- (2)
- (2)
- (3)
- (2)
- (2)
- (3)
- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (3)
- (2)
- (2)
- (2)
- (5)
- (3)
- (1)
- (2)
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1,036
Medchemexpress LLC 10-Undecenoic acid | 112-38-9 | MFCD00004442 | 97.3% | 100 MG
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10-Undecenoic acid (Undecylenic acid) is an antifungal agent. It inhibits Aβ oligomerization, scavenges ROS, and inhibits μ-calpain activity. It has neuroprotective and anticancer effects on various tumors. Additionally, it inhibits C. albicans biofilm formation and MRSA infection, and suppresses quorum sensing signals of Bacillus subtilis and Pseudomonas aeruginosa.
- Antifungal agent
- Inhibits Aβ oligomerization
- Scavenges reactive oxygen species (ROS)
- Inhibits μ-calpain activity
- Possesses neuroprotective effects
- Exhibits anticancer effects on various tumors
- Inhibits C. albicans biofilm formation and MRSA infection
- Inhibits quorum sensing signals of Bacillus subtilis and Pseudomonas aeruginosa
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1,037
Accela Chembio Inc Suberic Acid Monomethyl Ester | 100g | 3946-32-5 | MFCD00004427 | 97+% | D: 1.047 | Shelf Life: 540 Days | Regular
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Suberic Acid Monomethyl Ester | 100g | 3946-32-5 | MFCD00004427 | 97+% | D: 1.047 | Shelf Life: 540 Days | Regular
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1,038
Indofine Chemical ADENOSINE, Products for Life Science, 58-61-7, 0.99, 25 gm
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ADENOSINE, Products for Life Science, 58-61-7, 0.99, 25 gm
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1,039
Medchemexpress LLC (S)-4-Azido-2-hydroxybutanoate dicyclohexylamine | C16H30N4O3 | 25 MG
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(S)-N3-HABA (DCHA) is a click chemistry reagent designed for high-efficiency binding between nucleic acids, lipids, proteins, and other molecules. This reagent is highly valued in various research fields due to its high yield, high specificity, and simplicity in reactions. It features an azide group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) and ring strain-promoted alkyne-azide cycloaddition (SPAAC).
- Specifically designed for click chemistry applications.
- Characterized by high yield, high specificity, and simplicity in reactions.
- Capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) and ring strain-promoted alkyne-azide cycloaddition (SPAAC).
- Useful for binding nucleic acids, lipids, proteins, and other molecules in diverse research applications.
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1,040
Medchemexpress LLC L-allylglycine hydrochloride | 195316-72-4 | MFCD06797042 | 98.0% | 151.59 g/mol | C5H10ClNO2 | 1 G
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L-allylglycine hydrochloride is the hydrochloride salt of L-allylglycine, an amino acid derivative that functions as a glutamate decarboxylase (GAD) inhibitor. It reduces GABA biosynthesis and is used in neuroscience research to model GABAergic disruption and convulsant activity.
- Inhibits glutamate decarboxylase (GAD), decreasing GABA production.
- Useful as a research tool to study GABAergic pathways and seizure mechanisms.
- Provided as a hydrochloride salt for improved solubility in aqueous media.
- Available in small research-scale quantities suitable for experimental use.
- Characterized by formula C5H10ClNO2 and molecular weight 151.59 g/mol.
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1,041
Matrix Scientific BOC-L-ALLYLGLYCINE . DCHA-1G
Boc-L-allylglycine . DCHA, 1g,C22H40N2O4, MFCD01321013, mw 396.58, [143979-15-1]
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1,042
eMolecules EMOLECULES INC
5000472521 BOC-S-2-PROPARGYLGLYCINE 25G
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1,043
eMolecules EMOLECULES INC
5000472911 BOC-S-2-PROPARGYLGLYCINE 10G
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1,044
eMolecules EMOLECULES INC
5000472980 S-2-ALLYLGLYCINE 5G
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1,045
eMolecules EMOLECULES INC
5000473278 FMOC-L-PROPARGYLGLYCINE 10G
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1,046
eMolecules EMOLECULES INC
5000473590 L-ALLYLGLYCINE 1G
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1,047
eMolecules EMOLECULES INC
5000473594 L-ALLYLGLYCINE 0.25G
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1,048
eMolecules EMOLECULES INC
5000483375 FMOC-S-2-PROPARGYLGLYCINE 1G
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1,049
eMolecules EMOLECULES INC
5000491887 L-PROPARGYLGLYCINE 10G
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1,050
eMolecules EMOLECULES INC
5000492016 L-PROPARGYLGLYCINE 1G
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