Brassinazole - 10mM in DMSO , CAS No.224047-41-0

CAS: 224047-41-0 Cat. No.: B422692 Molecular Weight: 327.81 EC Number: 678-200-8

GRADE & PURITY 10mM in DMSO

Synonyms

BRZ | A816179 | CHEBI:73177 | AKOS027320938 | 2,3-cs/ex-PinD | DTXSID1043708 | Sodium tetraborate (Na2B4O7) | 4-(4-chlorophenyl)-2-phenyl-3-(1,2,4-triazol-1-yl)-2-butanol | BCP31880 | Q27140358 | SCHEMBL17275511 | (Rac)-Brassinazole | B2829 | s6781 | SCHE

Storage

Store at -80°C

Shipped In

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Overview

Brassinazole has been used in phenotype analyses to detect morphological changes in G-protein β subunit agb1 mutants.

Specifications

Synonyms

BRZ | A816179 | CHEBI:73177 | AKOS027320938 | 2, 3-cs/ex-PinD | DTXSID1043708 | Sodium tetraborate (Na2B4O7) | 4-(4-chlorophenyl)-2-phenyl-3-(1, 2, 4-triazol-1-yl)-2-butanol | BCP31880 | Q27140358 | SCHEMBL17275511 | (Rac)-Brassinazole | B2829 | s6781 | SCHE

Specifications & Purity

10mM in DMSO

Biochemical and Physiological Mechanisms

Brassinazole can induce dwarfing and morphological changes in Arabidopsis thaliana, which results in similarity with brassinol-deficient mutants. These changes were neutralized by brassinolide treatment, suggesting that brassinazole was responsible for br

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

This product requires cold chain shipping. Ground and other economy services are not available.

Names and Identifiers

• Canonical Smiles: CC(C1=CC=CC=C1)(C(CC2=CC=C(C=C2)Cl)N3C=NC=N3)O
• IUPAC Name: 4-(4-chlorophenyl)-2-phenyl-3-(1,2,4-triazol-1-yl)butan-2-ol
• InChIKey: YULDTPKHZNKFEY-UHFFFAOYSA-N
• INCHI: 1S/C18H18ClN3O/c1-18(23,15-5-3-2-4-6-15)17(22-13-20-12-21-22)11-14-7-9-16(19)10-8-14/h2-10,12-13,17,23H,11H2,1H3
• Isomeric SMILES: CC(C1=CC=CC=C1)(C(CC2=CC=C(C=C2)Cl)N3C=NC=N3)O
• Molecular Weight: 327.81
• Reaxy-Rn: 8267246
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8267246&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Phenylpropanoids and polyketides
    • Class Linear 1,3-diarylpropanoids

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Class: Linear 1,3-diarylpropanoids
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Linear 1,3-diarylpropanoids
• Alternative Parents: Amphetamines and derivatives Chlorobenzenes Aryl chlorides Triazoles Tertiary alcohols Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organochlorides Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Linear 1,3-diarylpropanoid - Amphetamine or derivatives - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Azole - Heteroaromatic compound - 1,2,4-triazole - Tertiary alcohol - Azacycle - Organoheterocyclic compound - Organochloride - Organohalogen compound - Aromatic alcohol - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as linear 1,3-diarylpropanoids. These are organic compounds with a structure based on a C6-C3-C6 skeleton, where the two benzene rings are not linked together.
• External Descriptors: tertiary alcohol - monochlorobenzenes - triazoles

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Oryza sativa (2923 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Molecular Weight: 327.800 g/mol
• XLogP3: 3.600
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 327.114 Da
• Monoisotopic Mass: 327.114 Da
• Topological Polar Surface Area: 50.900 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 369.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 2
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Xiao Shenghua, Hu Qin, Zhang Xiaojun, Si Huan, Liu Shiming, Chen Lin, Chen Kun, Berne Sabina, Yuan Daojun, Lindsey Keith, Zhang Xianlong, Zhu Longfu.  (2021)  Orchestration of plant development and defense by indirect crosstalk of salicylic acid and brassinosteorid signaling via transcription factor GhTINY2.  JOURNAL OF EXPERIMENTAL BOTANY,  72  (13): (4721-4743).  [PMID:33928361] [10.1093/jxb/erab186]

2. Hou Yuzhuo, Xu Mingzhi, Zhou Qinying, Yuan Feng, Yan Jianping, Liu Yanrong, Zhang Wanjun.  (2026)  MsRH53 is involved in brassinolide biosynthesis and positively regulates the salt tolerance in alfalfa.  PLANT SCIENCE,      [PMID:] [10.1016/j.plantsci.2026.113212]