Grouped product items

SKU

Size

Availability

Price

Qty

A102331-5g

In stock

$14.90

A102331-25g

25g

In stock

$56.90

A102331-100g

100g

In stock

$201.90

A102331-500g

500g

Available within 4-8 weeks(?)

$908.90

Basic Description

Synonyms	2-(4-sulfamoylphenyl)ethylamine \| 2-(4-sulfamoyl-phenyl)-ethyl-amine \| 4-(2-amino ethyl)benzene sulfonamide \| 4-(2-Aminoethyl)benzenesulphonamide \| P-AMINOETHYL BENZENESULFONAMIDE \| SCHEMBL142107 \| TimTec1_004114 \| D70143 \| J-523914 \| 4-(2-AMINOETHYL)BENZ
Specifications & Purity	≥99%
Shipped In	Normal
Product Description	Product Introduction The human hepatocellular carcinoma (HCC) cells were treated with its inhibitor 4-(2-aminoethyl)benzenesulfonamide. Application 4-(2-Aminoethyl)benzenesulfonamide was used to develop a model system to study the implementation of a microfluid chip required for Fourier transform measurements of biochemical interactions.

Associated Targets(Human)

CA6 Tclin Carbonic anhydrase 6 (3 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA1 Tclin Carbonic anhydrase 1 (2 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA2 Tclin Carbonic anhydrase 2 (58 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA4 Tclin Carbonic anhydrase 4 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA12 Tclin Carbonic anhydrase 12 (4 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA9 Tclin Carbonic anhydrase 9 (12 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA7 Tclin Carbonic anhydrase 7 (2 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

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

CA3 Tclin Carbonic anhydrase III (753 Activities)

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

CA6 Tclin Carbonic anhydrase VI (993 Activities)

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

CA1 Tclin Carbonic anhydrase I (13240 Activities)

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

CA5B Tclin Carbonic anhydrase VB (957 Activities)

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

CA5A Tclin Carbonic anhydrase VA (1168 Activities)

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

CA14 Tclin Carbonic anhydrase XIV (1305 Activities)

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

CA12 Tclin Carbonic anhydrase XII (6231 Activities)

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

CA9 Tclin Carbonic anhydrase IX (8255 Activities)

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

HepG2 (196354 Activities)

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

GMNN Tbio Geminin (128009 Activities)

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

CA2 Tclin Carbonic anhydrases; II & IX (262 Activities)

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

Associated Targets(non-human)

Ca7 Carbonic anhydrase VII (3 Activities)

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

Ca13 Carbonic anhydrase XIII (322 Activities)

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

CA4 Carbonic anhydrase IV (1713 Activities)

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

Carbonic anhydrase (69 Activities)

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

cynT Carbonic anhydrase 1 (82 Activities)

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

rep Replicase polyprotein 1ab (378 Activities)

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

Ca15 Carbonic anhydrase 15 (173 Activities)

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

mtcA1 Uncharacterized protein Rv1284/MT1322 (182 Activities)

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

PROBABLE TRANSMEMBRANE CARBONIC ANHYDRASE (CARBONATE DEHYDRATASE) (CARBONIC DEHYDRATASE) (107 Activities)

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

Malassezia furfur (70 Activities)

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

TGR Thioredoxin glutathione reductase (28579 Activities)

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

CA Alpha carbonic anhydrase (93 Activities)

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

CAN2 Carbonic anhydrase 2 (140 Activities)

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

Astrosclerin-3 (80 Activities)

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

Malassezia pachydermatis (160 Activities)

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

ca1 Delta carbonic anhydrase (40 Activities)

Discover Target: ca1

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

1272966 AGAP002992-PA (40 Activities)

Discover Target: 1272966

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

Carbonic anhydrase, alpha family (44 Activities)

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

Carbonate dehydratase (40 Activities)

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

SARS-CoV-2 (38078 Activities)

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

Names and Identifiers

Pubchem Sid	488188431
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488188431
IUPAC Name	4-(2-aminoethyl)benzenesulfonamide
INCHI	InChI=1S/C8H12N2O2S/c9-6-5-7-1-3-8(4-2-7)13(10,11)12/h1-4H,5-6,9H2,(H2,10,11,12)
InChi Key	FXNSVEQMUYPYJS-UHFFFAOYSA-N
Canonical SMILES	C1=CC(=CC=C1CCN)S(=O)(=O)N
Isomeric SMILES	C1=CC(=CC=C1CCN)S(=O)(=O)N
WGK Germany	3
PubChem CID	169682
UN Number	3259
Packing Group	III
Molecular Weight	200.26
Beilstein	14(3)2234
Reaxy-Rn	880588

Certificates

Certificate of Analysis(COA)

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10 results found

Lot Number	Certificate Type	Date	Item
C2429080	Certificate of Analysis	Apr 15, 2024	A102331
C2024184	Certificate of Analysis	Jan 15, 2024	A102331
B2228027	Certificate of Analysis	Mar 03, 2022	A102331
B2209066	Certificate of Analysis	Jan 12, 2022	A102331
B2209079	Certificate of Analysis	Jan 12, 2022	A102331
B2209081	Certificate of Analysis	Jan 12, 2022	A102331
B2209083	Certificate of Analysis	Jan 12, 2022	A102331
B2322221	Certificate of Analysis	Jan 12, 2022	A102331
B2322272	Certificate of Analysis	Jan 12, 2022	A102331
B2322273	Certificate of Analysis	Jan 12, 2022	A102331

Chemical and Physical Properties

Sensitivity	Air sensitive
Melt Point(°C)	150-152°C

Safety and Hazards(GHS)

Pictogram(s)	GHS05, GHS07
Signal	Danger
Hazard Statements	H315:Causes skin irritation H319:Causes serious eye irritation H335:May cause respiratory irritation H314:Causes severe skin burns and eye damage H302:Harmful if swallowed
Precautionary Statements	P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P405:Store locked up. P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P260:Do not breathe dust/fume/gas/mist/vapors/spray. P271:Use only outdoors or in a well-ventilated area. P270:Do not eat, drink or smoke when using this product. P301+P330+P331:IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing. P363:Wash contaminated clothing before reuse. P403+P233:Store in a well-ventilated place. Keep container tightly closed. P362+P364:Take off contaminated clothing and wash it before reuse. P330:Rinse mouth. P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes. P301+P317:IF SWALLOWED: Get medical help. P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing. P337+P317:If eye irritation persists: Get medical help. P332+P317:If skin irritation occurs: Get medical help. P302+P361+P354:IF ON SKIN: Take off Immediately all contaminated clothing. Immediately rinse with water for several minutes. P316:Get emergency medical help immediately. P319:Get medical help if you feel unwell.
WGK Germany	3
Reaxy-Rn	880588
Class	8

Citations of This Product

1. Guorong Ma, Ruiqiang Xu, Wang Pei, Yang Zhang, Rui Ma, Rang Yang, Zhihao Zhao, Yating Li, Chenjie Feng, Dongwu Jin, Wei Ma, Yumei Ma, Zhongren Ma. (2024) Screening and validation of an alkaline-tolerant biomimetic affinity chromatography A5–87 resin for purification of discarded bovine serum Immunoglobulin G. JOURNAL OF CHROMATOGRAPHY A, 1714 (464580). [PMID:38154349]

References

1. C H Mastrangelo,L D Williams,T Ghosh. (2010-11-26) Probing protein binding spectra with Fourier microfluidics.. Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference, 2010 (5318-5321). [PMID:21096068]
2. Su-jong Yu,Jung-hwan Yoon,Jeong-hoon Lee,Sun-jung Myung,Eun-sun Jang,Min-sun Kwak,Eun-ju Cho,Ja-june Jang,Yoon-jun Kim,Hyo-suk Lee. (2011-06-15) Inhibition of hypoxia-inducible carbonic anhydrase-IX enhances hexokinase II inhibitor-induced hepatocellular carcinoma cell apoptosis.. Acta pharmacologica Sinica, 32 ((7)): (912-920). [PMID:21666701]
3. Shanshan Qin,Yiran Ren,Xu Fu,Jie Shen,Xin Chen,Quan Wang,Xin Bi,Wenjing Liu,Lixin Li,Guangxin Liang,Cheng Yang,Wenqing Shui. (2015-09-01) Multiple ligand detection and affinity measurement by ultrafiltration and mass spectrometry analysis applied to fragment mixture screening.. Analytica chimica acta, 886 (98-106). [PMID:26320641]
4. Gayan S Jayawickrama,Alireza Nematollahi,Guanchen Sun,William Bret Church. (2018-04-25) Improvement of kynurenine aminotransferase-II inhibitors guided by mimicking sulfate esters.. PloS one, 13 ((4)): (e0196404-e0196404). [PMID:29689093]
5. P Megyeri,K M Pabst,M J Pabst. (1995-12-01) Serine protease inhibitors block priming of monocytes for enhanced release of superoxide.. Immunology, 86 ((4)): (629-635). [PMID:8567031]
6. Layne D Williams,Tridib Ghosh,Carlos H Mastrangelo. (2010-06-24) Low noise detection of biomolecular interactions with signal-locking surface plasmon resonance.. Analytical chemistry, 82 ((14)): (6025-6031). [PMID:20568712]
7. Takuya Mizumura,Keita Kondo,Masatoshi Kurita,Yutaka Kofuku,Mei Natsume,Shunsuke Imai,Yutaro Shiraishi,Takumi Ueda,Ichio Shimada. (2020-03-25) Activation of adenosine A2A receptor by lipids from docosahexaenoic acid revealed by NMR.. Science advances, 6 ((12)): (eaay8544-eaay8544). [PMID:32206717]
8. Guorong Ma, Ruiqiang Xu, Wang Pei, Yang Zhang, Rui Ma, Rang Yang, Zhihao Zhao, Yating Li, Chenjie Feng, Dongwu Jin, Wei Ma, Yumei Ma, Zhongren Ma. (2024) Screening and validation of an alkaline-tolerant biomimetic affinity chromatography A5–87 resin for purification of discarded bovine serum Immunoglobulin G. JOURNAL OF CHROMATOGRAPHY A, 1714 (464580). [PMID:38154349]

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4-(2-Aminoethyl)benzenesulfonamide - 99%, high purity , CAS No.35303-76-5

Basic Description

Associated Targets(Human)

Associated Targets(non-human)

Names and Identifiers

Certificates

Certificate of Analysis(COA)

Chemical and Physical Properties

Safety and Hazards(GHS)

Related Documents

Citations of This Product

References

Solution Calculators

Molarity Calculator

Dilution Calculator

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