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IUPAC Name: 
propyl 2-acetamido-3-methylpentanoate
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Enamine MADE BBs
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1 g
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Zoom the structure CSCS00010556516 Add to cart
IUPAC Name: 
propyl 2-cyclopentyl-2-acetamidoacetate
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Enamine MADE BBs
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Zoom the structure CSCS00038220232 Add to cart
IUPAC Name: 
propyl 2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-3-methylpentanoate
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Enamine MADE BBs
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Zoom the structure CSCS00135330516 Add to cart
IUPAC Name: 
(3S,6R,9R,13R)-9-benzyl-3-[(2R)-butan-2-yl]-13-[(2R)-hexan-2-yl]-6-methyl-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone
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Apollo Scientific
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1 g
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Description: CAS: 221111-70-2
Apollo Scientific USA
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1 g
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Description: CAS: 221111-70-2
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Zoom the structure CSCS21176532961 Add to cart
IUPAC Name: 
(3R,6S,9S)-6-benzyl-3-[(2S)-butan-2-yl]-13-(hexan-2-yl)-9-[(1H-indol-3-yl)methyl]-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone
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MedChemExpress
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1 mg
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Description: Names: Beauverolide Ja; Product Description: Beauverolide Ja, a cyclotetradepsipeptide, is a potent calmodulin (CaM) inhibitor with a Kd of 0.078 μM and a Ki of 0.39 μM for Ca2 -CaM. Beauverolide Ja is a secondary metabolite of Isaria fumosorosea; Target: Calmodulin;Endogenous Metabolite; CAS: 76265-41-3
MedChemExpress EU
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Description: Names: Beauverolide Ja; Product Description: Beauverolide Ja, a cyclotetradepsipeptide, is a potent calmodulin (CaM) inhibitor with a Kd of 0.078 μM and a Ki of 0.39 μM for Ca2 -CaM. Beauverolide Ja is a secondary metabolite of Isaria fumosorosea; Target: Calmodulin;Endogenous Metabolite; CAS: 76265-41-3
Targetmol Chemicals Inc
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1 mg
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Description: Beauverolide Ja, a cyclotetradepsipeptide and secondary metabolite of Isaria fumosorosea [1], functions as a potent inhibitor of calmodulin (CaM), exhibiting a dissociation constant (Kd) of 0.078 μM and an inhibition constant (Ki) of 0.39 μM for Ca2 -CaM.; CAS: 76265-41-3
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Zoom the structure CSCS06744597639 Add to cart
IUPAC Name: 
({4-[2-(2-amino-3-hydroxypropanamido)-4-carbamoylbutanamido]-5-{[2-(2-amino-3-methylpentanamido)-3-methylpentanoyl]oxy}-5-oxopentanoyl}oxy)phosphonic acid
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10X CHEM
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1 g
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Description: Alphostatin; CAS: 90119-88-3
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Zoom the structure CSCS21298300029 Add to cart
IUPAC Name: 
(3R,6S,9S,13S)-6-benzyl-3-[(2S)-butan-2-yl]-9-[(1H-indol-3-yl)methyl]-13-[(2S)-octan-2-yl]-1-oxa-4,7,10-triazacyclotridecane-2,5,8,11-tetrone
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MedChemExpress
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1 mg
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Description: Names: Beauverolide Ka; Product Description: Beauverolide Ka, a cyclotetradepsipeptide, is a metabolite of Beauveria bassiana fungus. Beauverolide Ka stimulates glucose uptake in cultured rat L6 myoblasts at 50 μM. Beauverolide Ka exhibits protecting effects on HEI-OC1 cells at 10 μM and shows dose-dependent activity in both L6 myoblasts and myotubes; Target: Endogenous Metabolite; CAS: 76265-42-4
MedChemExpress EU
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Description: Names: Beauverolide Ka; Product Description: Beauverolide Ka, a cyclotetradepsipeptide, is a metabolite of Beauveria bassiana fungus. Beauverolide Ka stimulates glucose uptake in cultured rat L6 myoblasts at 50 μM. Beauverolide Ka exhibits protecting effects on HEI-OC1 cells at 10 μM and shows dose-dependent activity in both L6 myoblasts and myotubes; Target: Endogenous Metabolite; CAS: 76265-42-4
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Zoom the structure CSCS06744597640 Add to cart
CAS: 19914-20-6
IUPAC Name: 
(3S,6R,9S,12R,15S,18R)-3-[(2S)-butan-2-yl]-4,10,16-trimethyl-6,9,12,15,18-pentakis(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone
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Key Organics Limited (BIONET)
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10 days 310.20
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Advanced ChemBlock Inc
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10 days 475.00
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Description: Enniatin B1; CAS: 19914-20-6
MedChemExpress
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30 days 681.00
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Description: Names: Enniatin B1; Product Description: Enniatin B1 is a Fusarium mycotoxin. Enniatin B1 inhibits acyl-CoA: cholesterol acyltransferase (ACAT) activity with an IC50 of 73 μM in an enzyme assay using rat liver microsomes Enniatin B1 crosss the blood-brain barrier Enniatin B1 decreases the activation of ERK (p44/p42). Enniatin B1 inhibits moderately TNF-α-induced NF-κB activation; Target: Acyltransferase;ERK;NF-κB; CAS: 19914-20-6
MedChemExpress EU
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30 days 681.00
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Description: Names: Enniatin B1; Product Description: Enniatin B1 is a Fusarium mycotoxin. Enniatin B1 inhibits acyl-CoA: cholesterol acyltransferase (ACAT) activity with an IC50 of 73 μM in an enzyme assay using rat liver microsomes Enniatin B1 crosss the blood-brain barrier Enniatin B1 decreases the activation of ERK (p44/p42). Enniatin B1 inhibits moderately TNF-α-induced NF-κB activation; Target: Acyltransferase;ERK;NF-κB; CAS: 19914-20-6
Targetmol Chemicals Inc
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30 days
718.00
1 mg
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Description: Enniatin B1, a Fusarium mycotoxin, crosses the blood-brain barrier, decreases the activation of ERK (p44/p42), and inhibits moderately TNF-α-induced NF-κB activation. Furthermore, it inhibits acyl-CoA: cholesterol acyltransferase (ACAT) activity, exhibiting an IC50 of 73 μM in rat liver microsome enzyme assays.; CAS: 19914-20-6
Alfa Chemistry Analytical Products
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7 days
POA
1 g
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Description: CAS: 19914-20-6
Aldlab Chemicals LLC
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POA
1 g
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Description: CAS: 19914-20-6
Crysdot LLC
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1 g
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Description: CAS: 19914-20-6
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Zoom the structure CSCS00161002230 Add to cart
IUPAC Name: 
(3R,6S,9R,12S,15R,18S)-3-[(2R)-butan-2-yl]-4,10,16-trimethyl-6,9,12,15,18-pentakis(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone
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Apollo Scientific
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1 g
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Description: CAS: 19914-20-6
Apollo Scientific USA
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1 g
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Description: CAS: 19914-20-6
BioBioPha Co., Ltd.
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1 g
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Description: CAS: 19914-20-6
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Zoom the structure CSCS21176529479 Add to cart
IUPAC Name: 
(3S,6R,9S,12R,15S,18R)-3,9-bis[(2S)-butan-2-yl]-4,10,16-trimethyl-6,12,15,18-tetrakis(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone
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Key Organics Limited (BIONET)
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10 days 474.10
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Targetmol Chemicals Inc
Ships from: United States
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30 days
718.00
1 mg
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Description: Enniatin A1, a cyclic hexadepsipeptide composed of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids isolated from Fusarium mycotoxins, exhibits anticarcinogenic effects through the induction of apoptosis and disruption of the ERK signaling pathway. It also inhibits ACAT in rat liver microsomes with an IC50 of 49 μM.; CAS: 4530-21-6
Alfa Chemistry Analytical Products
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7 days
POA
1 g
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Description: CAS: 4530-21-6
BOC Sciences
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POA
1 g
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Description: CAS: 4530-21-6
Zerenex Molecular Ltd
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1 g
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Description: CAS: 4530-21-6
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Zoom the structure CSCS00116208316 Add to cart
IUPAC Name: 
(3S,6R,12R,15S,18R)-3,9-bis[(2S)-butan-2-yl]-4,10,16-trimethyl-6,12,15,18-tetrakis(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone
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MedChemExpress
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30 days
389.00
1 mg
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Description: Names: Enniatin A1; Product Description: Enniatin A1 isolated from Fusarium mycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids. Enniatin A1 possesses anticarcinogenic properties by induction of apoptosis and disruption of ERK signalling pathway. Enniatin A1 inhibits ACAT with an IC50 of 49 μM in rat liver microsomes; Target: Apoptosis;ERK; CAS: 4530-21-6
MedChemExpress EU
Ships from: Sweden
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30 days
389.00
1 mg
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Description: Names: Enniatin A1; Product Description: Enniatin A1 isolated from Fusarium mycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids. Enniatin A1 possesses anticarcinogenic properties by induction of apoptosis and disruption of ERK signalling pathway. Enniatin A1 inhibits ACAT with an IC50 of 49 μM in rat liver microsomes; Target: Apoptosis;ERK; CAS: 4530-21-6
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Zoom the structure CSCS02495325221 Add to cart
IUPAC Name: 
(3S,6R,9S,12R,15S,18R)-3,9-bis(butan-2-yl)-4,10,16-trimethyl-6,12,15,18-tetrakis(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone
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Apollo Scientific
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1 g
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Description: CAS: 4530-21-6
Apollo Scientific USA
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1 g
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Description: CAS: 4530-21-6
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Zoom the structure CSCS06645152087 Add to cart
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