Camalexin - ≥98% , CAS No.135531-86-1

CAS: 135531-86-1 Cat. No.: C412537 분자식: C11H8N2S 분자량: 200.26 EC 번호: 808-542-7
주문 가능
GRADE & PURITY ≥98%
Synonyms
AS-16652 | Q19903715 | 1H-indole, 3-(2-thiazolyl)- | QY3Z69LA99 | 3-thiazol-2'-yl-indole | 3-(thiazol-2-yl)indole | AKOS030257626 | 3-(Thiazol-2-yl)-1H-indole | SCHEMBL343413 | 2-(1H-indol-3-yl)-1,3-thiazole | 3-(2-Thiazolyl)-1H-indole | HY-119502 | Camal
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
★
Size
USA
독일 (EU)*
Price
Qty
5mg
C412537-5mg
3 재고 있음
—

US$28.90

US$43.90
저장 US$15.00 (34.17%)
25mg
C412537-25mg
2 재고 있음
—

US$105.90

US$158.90
저장 US$53.00 (33.35%)
100mg
C412537-100mg
2 재고 있음
—

US$282.90

US$424.90
저장 US$142.00 (33.42%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

개요

Camalexin is a phytoalexin isolated from Camelina sativa (Cruciferae) with antibacterial, antifungal, antiproliferative and anticancer activities. Camalexin can induce reactive oxygen species (ROS) production。

Information

Camalexin Camalexin, a phytoalexin isolated from Camelina sativa and Arabidopsis (Cruciferae), can induce reactive oxygen species (ROS) production. Camalexin has antibacterial, antifungal, antiproliferative and anticancer activities.

Specifications

동의어
AS-16652 | Q19903715 | 1H-indole, 3-(2-thiazolyl)- | QY3Z69LA99 | 3-thiazol-2'-yl-indole | 3-(thiazol-2-yl)indole | AKOS030257626 | 3-(Thiazol-2-yl)-1H-indole | SCHEMBL343413 | 2-(1H-indol-3-yl)-1,3-thiazole | 3-(2-Thiazolyl)-1H-indole | HY-119502 | Camal
사양 및 순도
≥98%
생화학 및 생리적 메커니즘
Camalexin, a phytoalexin isolated from Camelina sativa and Arabidopsis (Cruciferae), can induce reactive oxygen species (ROS) production. Camalexin has antibacterial, antifungal, antiproliferative and anticancer activities.
보관 조건
Store at -20°C
배송
Ice chest + Ice pads
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순수함
≥98%
이름과 식별자
Pubchem Sid528772256
정식 스마일C1=CC=C2C(=C1)C(=CN2)C3=NC=CS3
IUPAC Name2-(1H-indol-3-yl)-1,3-thiazole
InChIKeyIYODIJVWGPRBGQ-UHFFFAOYSA-N
INCHI1S/C11H8N2S/c1-2-4-10-8(3-1)9(7-13-10)11-12-5-6-14-11/h1-7,13H
이성체 SMILES C1=CC=C2C(=C1)C(=CN2)C3=NC=CS3
WGK 독일 3
분자량 200.26
Reaxy-Rn 4310041
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4310041&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
분류Indoles and derivatives
SubclassIndoles
Intermediate Tree Nodes Not available
Direct ParentIndoles
Alternative Parents Substituted pyrroles  Benzenoids  Thiazoles  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indole - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Thiazole - Pyrrole - Azole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
설명This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
External Descriptors an indole-phytolexin
3D 구조
상호 작용 화학 구조 모델





관련 대상(비인간)
Plenodomus lingam (178 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
작용 메커니즘
인증서(CoA, COO, BSE/TSE 및 분석 차트)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate Type날짜항목
L2321077Certificate of AnalysisSep 21, 2026 C412537
L2321079Certificate of AnalysisSep 21, 2026 C412537
L2321161Certificate of AnalysisSep 21, 2026 C412537
L2321163Certificate of AnalysisSep 21, 2026 C412537
L2321076Certificate of AnalysisDec 11, 2023 C412537
화학 및 물리적 특성
용해성Solubility (25°C) In vitro Ethanol: mg/mL    
분자량200.260 g/mol
XLogP32.700
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass200.041 Da
Monoisotopic Mass200.041 Da
Topological Polar Surface Area56.900 Ų
Heavy Atom Count14
Formal Charge0
Complexity209.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
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