Anhydroophiobolin A

Modify Date: 2025-08-25 12:47:39

Anhydroophiobolin A Structure
Anhydroophiobolin A structure
Common Name Anhydroophiobolin A
CAS Number 6026-65-9 Molecular Weight 382.53600
Density N/A Boiling Point N/A
Molecular Formula C25H34O3 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Anhydroophiobolin A


Anhydroophiobolin A is a potent inhibitor of photosynthesis with IC50s of 77 and 14 mM in the photosynthesis of chlorella and spinach, respectively. Anhydroophiobolin A is an analog of Ophiobolin A[1].

 Names

Name 3-Anhydrocochliobolin
Synonym More Synonyms

 Anhydroophiobolin A Biological Activity

Description Anhydroophiobolin A is a potent inhibitor of photosynthesis with IC50s of 77 and 14 mM in the photosynthesis of chlorella and spinach, respectively. Anhydroophiobolin A is an analog of Ophiobolin A[1].
Related Catalog
References

[1]. Jin-Myeon KIM, et al. Isolation of Ophiobolin A and Its Analogs as Inhibitors to Photosynthesis.

 Chemical & Physical Properties

Molecular Formula C25H34O3
Molecular Weight 382.53600
Exact Mass 382.25100
PSA 43.37000
LogP 5.21320

 Synonyms

3-anhydroophiobolin a (14,17-epoxy-5-oxo-3,7,18-ophiobolatrien-21-al)
anhydroophiobolin a
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here


Get all suppliers and price by the below link:

Anhydroophiobolin A suppliers

Anhydroophiobolin A price

Related Compounds: More...
actinoplanone A
115655-86-2
Thapsuine A
76429-00-0
Apocynol A
358721-33-2
(2S)-N-[(2S,5S,8S,11R,12S,15S,18S,21R)-5-[(3-bromo-4-methoxyphenyl)methyl]-2-[(2S)-butan-2-yl]-15-[3-(carbamoylamino)propyl]-21-hydroxy-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-8-propan-2-yl-10-oxa-1,4,7,14,17-pentazabicyclo[16.3.1]docosan-12-yl]-2-(butanoyla
1007391-44-7
Pseudoanguillosporin A
1159392-22-9
Digitoside A
140208-79-3
Tirandamycin A
34429-70-4
Blattellastanoside A
149864-63-1
amaronol a
226560-96-9
(2S,4S)-1-{2-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-1,3-thiazole-5-carbonyl}-4-hydroxypyrrolidine-2-carboxylic acid
2171160-07-7
2-({5-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-1,3-oxazol-4-yl}formamido)-3-hydroxy-2-methylpropanoic acid
2171925-84-9
3-(N-ethyl-1-{2-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-1,3-thiazol-5-yl}formamido)butanoic acid
2172081-93-3
3-[(2S,3S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylpentanoyl]-3-azabicyclo[4.1.0]heptane-7-carboxylic acid
2171323-04-7
(2R)-1-[(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-(methylsulfanyl)butanoyl]-2-methylpyrrolidine-2-carboxylic acid
2171155-54-5
1-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylbutanoyl]-4,4-dimethylpyrrolidine-3-carboxylic acid
2171638-43-8
2-[(1RS,3SR)-3-[(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]cyclopentyl]acetic acid
2227685-77-8
3-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2,4-trimethylpentanamido]-3-methylbutanoic acid
2172020-98-1
(2S)-2-({3-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]cyclohexyl}formamido)-3-methylbutanoic acid
2648916-53-2
(2S,4R)-1-{5-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]oxolane-3-carbonyl}-4-hydroxypyrrolidine-2-carboxylic acid
2648930-01-0