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Details

Stereochemistry ABSOLUTE
Molecular Formula C19H21O6.K
Molecular Weight 384.4647
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of POTASSIUM GIBBERELLATE

SMILES

[K+].[H][C@@]12CC[C@]3(O)C[C@]1(CC3=C)[C@@H](C([O-])=O)[C@]4([H])[C@@]5(C)[C@@H](O)C=C[C@@]24OC5=O

InChI

InChIKey=BGJIAUDTIACQSC-GLDAWBHVSA-M
InChI=1S/C19H22O6.K/c1-9-7-17-8-18(9,24)5-3-10(17)19-6-4-11(20)16(2,15(23)25-19)13(19)12(17)14(21)22;/h4,6,10-13,20,24H,1,3,5,7-8H2,2H3,(H,21,22);/q;+1/p-1/t10-,11+,12-,13-,16-,17+,18+,19-;/m1./s1

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including http://www.rarexoticseeds.com/en/gibberellic-acid-powder-ga3-90.html http://www.lifesciencesite.com/lsj/life0803/060_6326life0803_373_383.pdf

Gibberellic acid was first discovered in Japan in 1935 as a result of the study of a condition common in rice plants called "foolish seedling" disease, which caused the plants to grow much taller than normal. The effects of gibberellins weren't widely understood until years later. Gibberellic acid, GA3 is a naturally occurring plant hormone that regulates the growth of plants, including triggering seed germination. Gibberellic Acid is not manufactured; it's a natural product extracted from the Gibberella fujikuroi fungus. There are over 100 known forms of gibberellic acid; GA3 is the most effective. Gibberellic acid (GA3) is used extensively in Egypt and other countries, to increase the growth of many fruits (such as strawberries and grapes) and vegetables (such as tomatoes, cabbages and cauliflower). Carcinogenic effect of Gibberellic acid has being demonstrated in several studies. Gibberellic acid increased the activity of testicular 3β-HSD and 17β-HSD and elevated testosterone content in rats, acting as an agonist of steroidogenesis in male rats. Gibberellic acid has being suggested to promote ulcer-healing, healing of surgical wounds or open fractures and treatment of bronchitis or thrombophlebitis in animals including humans.

CNS Activity

Curator's Comment: shown in rats

Originator

Curator's Comment: Gibberellic acid was first discovered in Japan in 1935

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown

Sample Use Guides

In Vivo Use Guide
Rats:100 - 200 ppm of Gibberellic acid daily in drinking tap water for eight weeks, Gibberellic acid amount of each rat was about 3± 0.3mg - 6± 0.6 mg per
Route of Administration: Oral
150 ug of gibberellic acid increased the levels of StAR protein and ABP in the rat testis
Name Type Language
POTASSIUM GIBBERELLATE
FCC  
Common Name English
K-GA
Common Name English
GIBB-3-ENE-1,10-DICARBOXYLIC ACID, 2,4A,7-TRIHYDROXY-1-METHYL-8-METHYLENE-, 1,4A-LACTONE, MONOPOTASSIUM SALT, (1.ALPHA.,2.BETA.,4A.ALPHA.,4B.BETA.,10.BETA.)-
Common Name English
GIBBERELLIC ACID, MONOPOTASSIUM SALT
Common Name English
GIBBERELLIC ACID, POTASSIUM SALT
Common Name English
POTASSIUM GIBBERELLATE [FCC]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 172.725
Created by admin on Sat Dec 16 04:48:04 GMT 2023 , Edited by admin on Sat Dec 16 04:48:04 GMT 2023
EPA PESTICIDE CODE 43802
Created by admin on Sat Dec 16 04:48:04 GMT 2023 , Edited by admin on Sat Dec 16 04:48:04 GMT 2023
Code System Code Type Description
MESH
C007842
Created by admin on Sat Dec 16 04:48:04 GMT 2023 , Edited by admin on Sat Dec 16 04:48:04 GMT 2023
PRIMARY
CAS
125-67-7
Created by admin on Sat Dec 16 04:48:04 GMT 2023 , Edited by admin on Sat Dec 16 04:48:04 GMT 2023
PRIMARY
FDA UNII
H52L7VZB7S
Created by admin on Sat Dec 16 04:48:04 GMT 2023 , Edited by admin on Sat Dec 16 04:48:04 GMT 2023
PRIMARY
ALANWOOD
potassium gibberellate
Created by admin on Sat Dec 16 04:48:04 GMT 2023 , Edited by admin on Sat Dec 16 04:48:04 GMT 2023
PRIMARY
EPA CompTox
DTXSID6035605
Created by admin on Sat Dec 16 04:48:04 GMT 2023 , Edited by admin on Sat Dec 16 04:48:04 GMT 2023
PRIMARY
PUBCHEM
71299661
Created by admin on Sat Dec 16 04:48:04 GMT 2023 , Edited by admin on Sat Dec 16 04:48:04 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-749-6
Created by admin on Sat Dec 16 04:48:04 GMT 2023 , Edited by admin on Sat Dec 16 04:48:04 GMT 2023
PRIMARY