ATB 346 - 10mM in DMSO , CAS No.1226895-20-0

CAS: 1226895-20-0 Cat. No.: A420974 Summenformel: C₂₁H₁₉NO₃S Molekulargewicht: 365.45

GRADE & PURITY 10mM in DMSO

Synonyms

1226895-20-0|ATB-346|ATB 346|Otenaproxesul|4-carbamothioylphenyl 2-(6-methoxynaphthalen-2-yl)propanoate|(S)-atb-346|2-Naphthaleneacetic acid, 6-methoxy-alpha-methyl-, 4-(aminothioxomethyl)phenyl ester|3096O7WP53|(4-carbamothioylphenyl) 2-(6-methoxynaphtha

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

Information

ATB 346 ATB 346, a novel hydrogen sulphide-releasing derivative of naproxen with remarkably reduced toxicity, inhibits COX activity. ATB 346 is an anti-inflammatory agent that induces apoptosis of human melanoma cells.

Targets

COX

Specifications

Synonyme

1226895-20-0 | ATB-346 | ATB 346 | Otenaproxesul | 4-carbamothioylphenyl 2-(6-methoxynaphthalen-2-yl)propanoate | (S)-atb-346 | 2-Naphthaleneacetic acid, 6-methoxy-alpha-methyl-, 4-(aminothioxomethyl)phenyl ester | 3096O7WP53 | (4-carbamothioylphenyl) 2-(6-methoxynaphtha

Spezifikationen & Reinheit

10mM in DMSO

Biochemische und physiologische Mechanismen

ATB 346, a novel hydrogen sulphide-releasing derivative of naproxen with remarkably reduced toxicity, inhibits COX activity. ATB 346 is an anti-inflammatory agent that induces apoptosis of human melanoma cells.

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Aktionsart

INHIBITOR

Produkteigenschaften

• ALogP: 4.521
• hba_count: 3
• HBD-Zahl: 1
• Rotationsfähige Bindung: 6

Namen und Kennungen

• Pubchem Sid: 528763168
• Kanonisches Lächeln: CC(C1=CC2=C(C=C1)C=C(C=C2)OC)C(=O)OC3=CC=C(C=C3)C(=S)N
• IUPAC Name: (4-carbamothioylphenyl) 2-(6-methoxynaphthalen-2-yl)propanoate
• InChIKey: YCNMAPLPQYQJFC-UHFFFAOYSA-N
• INCHI: 1S/C21H19NO3S/c1-13(21(23)25-18-8-5-14(6-9-18)20(22)26)15-3-4-17-12-19(24-2)10-7-16(17)11-15/h3-13H,1-2H3,(H2,22,26)
• Isomere SMILES: CC(C1=CC2=C(C=C1)C=C(C=C2)OC)C(=O)OC3=CC=C(C=C3)C(=S)N
• Molekulargewicht: 365.45
• Reaxy-Rn: 12656874
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=12656874&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Naphthalenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Naphthalenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Naphthalenes
• Alternative Parents: Phenol esters Phenoxy compounds Anisoles Alkyl aryl ethers Thioamides Carboxylic acid esters Thiocarboxylic acid amides Monocarboxylic acids and derivatives Thiocarbonyl compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Phenol ester - Naphthalene - Phenoxy compound - Anisole - Alkyl aryl ether - Monocyclic benzene moiety - Thioamide - Carboxylic acid ester - Thiocarboxylic acid amide - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Thiocarbonyl group - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic homopolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
• External Descriptors: Not available

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

Zugehörige Ziele (menschlich)

HepG2 (196354 Activities)

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L02 (4864 Activities)

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Zugehörige Ziele (nicht menschlich)

Nos2 Nitric oxide synthase, inducible (3573 Activities)

Discover Target: Nos2

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Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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RAW264.7 (28094 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• DMSO (mg/ml) Maximale Löslichkeit: 73
• DMSO (mM) Maximale Löslichkeit: 199.753728280202
• Wasser (mg/ml) Maximale Löslichkeit: ＜1
• Molekulargewicht: 365.400 g/mol
• XLogP3: 4.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 365.109 Da
• Monoisotopic Mass: 365.109 Da
• Topological Polar Surface Area: 93.600 Ų
• Heavy Atom Count: 26
• Formal Charge: 0
• Complexity: 503.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1