Jump to main content Jump to site nav

Visit the new version of ChemSpider

blastmycin

Molecular FormulaC₂₆H₃₆N₂O₉
Average mass520.572 Da
Monoisotopic mass520.242065 Da
ChemSpider ID215110

- 5 of 5 defined stereocentres

More details:

Featured data source

Names and Synonyms
Database ID(s)

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

(2R,3S,6S,7R,8R)-8-Butyl-3-[(3-formamido-2-hydroxybenzoyl)amino]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl 3-methylbutanoate [ACD/IUPAC Name]

(2R,3S,6S,7R,8R)-8-Butyl-3-[(3-formamido-2-hydroxybenzoyl)amino]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl-3-methylbutanoat [German] [ACD/IUPAC Name]

(2R,3S,6S,7R,8R)-8-butyl-3-{[3-(formylamino)-2-hydroxybenzoyl]amino}-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl 3-methylbutanoate (non-preferred name)

[2R-(2R*,3S*,6S*,7R*,8R*)]-3-Methylbutanoic Acid 8-Butyl-3-[[3-(formylamino)-2-hydroxybenzoyl]amino]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl Ester

116095-17-1 [RN]

208-335-6 [EINECS]

3-Méthylbutanoate de (2R,3S,6S,7R,8R)-8-butyl-3-[(3-formamido-2-hydroxybenzoyl)amino]-2,6-diméthyl-4,9-dioxo-1,5-dioxonan-7-yle [French] [ACD/IUPAC Name]

522-70-3 [RN]

antimycin A3

antimycin A3b

More...

blastmycin

Isovaleric Acid 8-Ester with N-(7-butyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-3-formamidosalicylamide

(+)-antimycin A3b

(2R,3S,6S,7R,8R)-8-butyl-3-(3-formamido-2-hydroxybenzamido)-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl 3-methylbutanoate

(2R,3S,6S,7R,8R)-8-butyl-3-[(3-formamido-2-hydroxybenzene)amido]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl 3-methylbutanoate

[(2R,3S,6S,7R,8R)-3-[(3-Formamido-2-hydroxybenzoyl)amino]-8-heptyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] (2R)-2-methylbutanoate

[(2R,3S,6S,7R,8R)-3-[(3-formamido-2-hydroxybenzoyl)amino]-8-hexyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] 2-methylpropanoate

[(2R,3S,6S,7R,8R)-3-[(3-formamido-2-hydroxy-benzoyl)amino]-8-hexyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] 2-methylpropanoate

[(2R,3S,6S,7R,8R)-3-[(3-formamido-2-hydroxy-phenyl)carbonylamino]-8-hexyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] 2-methylpropanoate

[(2R,3S,6S,7R,8R)-8-butyl-3-[(3-formamido-2-hydroxybenzoyl)amino]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] 3-methylbutanoate

[(2R,3S,6S,7R,8R)-8-butyl-3-[(3-formamido-2-hydroxy-benzoyl)amino]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] 3-methylbutanoate

[(2R,3S,6S,7R,8R)-8-butyl-3-[(3-formamido-2-hydroxy-phenyl)carbonylamino]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] 3-methylbutanoate

1397-94-0 [RN]

2(or 3)-methyl-butanoic acid, (2R,3S,6S,7R,8R)-3-[[3-(formylamino)-2-hydroxybenzoyl]amino]-8-butyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl ester

20734-66-1 [RN]

2-methylpropanoic acid [(2R,3S,6S,7R,8R)-3-[[(3-formamido-2-hydroxyphenyl)-oxomethyl]amino]-8-hexyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] ester

2-methylpropionic acid [(2R,3S,6S,7R,8R)-3-[(3-formamido-2-hydroxy-benzoyl)amino]-8-hexyl-4,9-diketo-2,6-dimethyl-1,5-dioxonan-7-yl] ester

3-methylbutanoic acid [(2R,3S,6S,7R,8R)-8-butyl-3-[[(3-formamido-2-hydroxyphenyl)-oxomethyl]amino]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl] ester

3-Methyl-butyric acid (2R,3S,6S,7R,8R)-8-butyl-3-(3-formylamino-2-hydroxy-benzoylamino)-2,6-dimethyl-4,9-dioxo-[1,5]dioxonan-7-yl ester

3-Methyl-butyric acid (2R,3S,6S,7R,8R)-8-butyl-3-{[1-(3-formylamino-2-hydroxy-phenyl)-methanoyl]-amino}-2,6-dimethyl-4,9-dioxo-[1,5]dioxonan-7-yl ester

3-methylbutyric acid [(2R,3S,6S,7R,8R)-8-butyl-3-[(3-formamido-2-hydroxy-benzoyl)amino]-4,9-diketo-2,6-dimethyl-1,5-dioxonan-7-yl] ester

3-Methyl-butyric acid 8-butyl-3-(3-formylamino-2-hydroxy-benzoylamino)-2,6-dimethyl-4,9-dioxo-[1,5]dioxonan-7-yl ester

58239-09-1 [RN]

A 80021F34

A1-Purothionin

A-3

Antimycin A

Blastomycin

Butanoic acid, 3-methyl-, 8-butyl-3-[[3- (formylamino)-2-hydroxybenzoyl]amino]-2, 6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl ester, [2R-(2R*,3S*,6S*, 7R*,8R*)]-

Butanoic acid, 3-methyl-, 8-butyl-3-[[3-(formylamino)-2-hydroxybenzoyl]amino]-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl ester, [2R-(2R*,3S*,6S*,7R*,8R*)]-

CHEMBL436605

https://www.ebi.ac.uk/chembl/compound_reportcard/CHEMBL436605/

Isovaleric acid, N-ester with N- (7-butyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1, 5-dioxonan-3-yl)-3-formamidosalicylamide, stereoisomer

Isovaleric acid, N-ester with N-(7-butyl-8-hydroxy-4,9-dimethyl-2,6-dioxo-1,5-dioxonan-3-yl)-3-formamidosalicylamide, stereoisomer

MFCD00869273

Peptide SP2

Purothionin AII

Threonine, N-(3-formamidosalicyloyl)-, 2-(1, 2-dihydroxypropyl)hexanoate, 7-lactone, isovalerate

Threonine, N-(3-formamidosalicyloyl)-, 2-(1,2-dihydroxypropyl)hexanoate, 7-lactone, isovalerate

UNII-7JMI3P2Y5R

UNII-8S75R39Y6J

WLN: T9OV EOVTJ CMVR CQ DMVH& D1 G4 HOVX1&1&1 I1

Less...

Validated by Experts, Validated by Users, Non-Validated, Removed by Users

97YBD5W80B [DBID]

AIDS012099 [DBID]

AIDS-012099 [DBID]

nchembio.94-comp32 [DBID]

NCI60_004417 [DBID]

NSC 58239 [DBID]

NSC58239 [DBID]

UNII:97YBD5W80B [DBID]

UNII-97YBD5W80B [DBID]

Experimental data
Predicted - ACD/Labs
Predicted - ChemAxon

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

Density:	1.3±0.1 g/cm³
Boiling Point:	745.5±60.0 °C at 760 mmHg
Vapour Pressure:	0.0±2.6 mmHg at 25°C
Enthalpy of Vaporization:	112.5±3.0 kJ/mol
Flash Point:	404.7±32.9 °C
Index of Refraction:	1.549
Molar Refractivity:	132.0±0.4 cm³
#H bond acceptors:	11
#H bond donors:	3
#Freely Rotating Bonds:	10
#Rule of 5 Violations:	2

ACD/LogP:	3.62
ACD/LogD (pH 5.5):	3.58
ACD/BCF (pH 5.5):	306.02
ACD/KOC (pH 5.5):	2087.26
ACD/LogD (pH 7.4):	3.31
ACD/BCF (pH 7.4):	167.05
ACD/KOC (pH 7.4):	1139.41
Polar Surface Area:	157 Å²
Polarizability:	52.3±0.5 10^-24cm³
Surface Tension:	53.8±5.0 dyne/cm
Molar Volume:	415.0±5.0 cm³

Click to predict properties on the Chemicalize site

Patents	Personal Collections
Publication or Magazine Article	Web-based Article (blog or commentary)
Available Chemicals Databases	Biological Properties
Chemical Reactions	Chemical Safety Data
Drugs or Compounds in Development	Imaging Agents
Information Aggregators	Journal Publishers via MeSH
Ligand/binding/crystal Structure Databases	Metabolic Pathways
Molecular Libraries Screening Center Network	Natural Products
NIH Substance Repository	Physical Properties (including SAR/QSAR databases)
Protein 3D Structures	Spectroscopy Databases
Substance Vendors	Theoretical Properties
Toxicology/Environmental Databases	Virtual Library

blastmycin

More details:

Search ChemSpider:

Search Google: