PBI-51
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MedKoo CAT#: 525972

CAS#: 130694-74-5

Description: PBI-51 is a competitive Inhibitor of Abscisic Acid-Regulated Gene Expression.


Chemical Structure

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PBI-51
CAS# 130694-74-5

Theoretical Analysis

MedKoo Cat#: 525972
Name: PBI-51
CAS#: 130694-74-5
Chemical Formula: C15H22O3
Exact Mass: 250.16
Molecular Weight: 250.338
Elemental Analysis: C, 71.97; H, 8.86; O, 19.17

Price and Availability

Size Price Availability Quantity
2.5mg USD 500
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Synonym: PBI-51

IUPAC/Chemical Name: (4S,5R)-4-hydroxy-4-((Z)-5-hydroxy-3-methylpent-3-en-1-ynyl)-3,3,5-trimethylcyclohexanone

InChi Key: WORLVFQFRWYCAV-CWJQNXGWSA-N

InChi Code: InChI=1S/C15H22O3/c1-11(6-8-16)5-7-15(18)12(2)9-13(17)10-14(15,3)4/h6,12,16,18H,8-10H2,1-4H3/b11-6-/t12-,15+/m1/s1

SMILES Code: O=C1CC(C)(C)[C@@](C#C/C(C)=C\CO)(O)[C@H](C)C1

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Product Data:
Biological target: PBI-51 is a competitive Inhibitor of Abscisic Acid-Regulated Gene Expression.
In vitro activity: PBI-51 displayed a reversible antagonistic effect with ABA, shifting the typical ABA dose-response curve by a factor of 4 to 5. This antagonism was noted for the expression of two ABA-sensitive genes, napin and oleosin. To test whether this antagonism was at the level of ABA recognition or uptake, ABA uptake was monitored in the presence of PBI-51 or PBI-63. Neither compound decreased ABA uptake. Treatments with either PBI-51 or PBI-63 showed an effect on endogenous ABA pools by permitting increases of 5- to 7-fold. Reference: Plant Physiol. 1993 Feb;101(2):469-476. https://pubmed.ncbi.nlm.nih.gov/12231700/
In vivo activity: TBD

Preparing Stock Solutions

The following data is based on the product molecular weight 250.34 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol: 1. Yamazaki D, Yoshida S, Asami T, Kuchitsu K. Visualization of abscisic acid-perception sites on the plasma membrane of stomatal guard cells. Plant J. 2003 Jul;35(1):129-39. doi: 10.1046/j.1365-313x.2003.01782.x. PMID: 12834408. 2. Wilen RW, Hays DB, Mandel RM, Abrams SR, Moloney MM. Competitive Inhibition of Abscisic Acid-Regulated Gene Expression by Stereoisomeric Acetylenic Analogs of Abscisic Acid. Plant Physiol. 1993 Feb;101(2):469-476. doi: 10.1104/pp.101.2.469. PMID: 12231700; PMCID: PMC160593.
In vitro protocol: 1. Yamazaki D, Yoshida S, Asami T, Kuchitsu K. Visualization of abscisic acid-perception sites on the plasma membrane of stomatal guard cells. Plant J. 2003 Jul;35(1):129-39. doi: 10.1046/j.1365-313x.2003.01782.x. PMID: 12834408. 2. Wilen RW, Hays DB, Mandel RM, Abrams SR, Moloney MM. Competitive Inhibition of Abscisic Acid-Regulated Gene Expression by Stereoisomeric Acetylenic Analogs of Abscisic Acid. Plant Physiol. 1993 Feb;101(2):469-476. doi: 10.1104/pp.101.2.469. PMID: 12231700; PMCID: PMC160593.
In vivo protocol: TBD

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1: Yamazaki D, Yoshida S, Asami T, Kuchitsu K. Visualization of abscisic acid-perception sites on the plasma membrane of stomatal guard cells. Plant J. 2003 Jul;35(1):129-39. PubMed PMID: 12834408.

2: Wilen RW, Hays DB, Mandel RM, Abrams SR, Moloney MM. Competitive Inhibition of Abscisic Acid-Regulated Gene Expression by Stereoisomeric Acetylenic Analogs of Abscisic Acid. Plant Physiol. 1993 Feb;101(2):469-476. PubMed PMID: 12231700; PubMed Central PMCID: PMC160593.