Fasnall - ≥99% , CAS No.929978-58-5

CAS: 929978-58-5 Cat. No.: F413416 Summenformel: C19H22N4S Molekulargewicht: 338.47
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GRADE & PURITY ≥99%
Synonyms
Thieno[2,​3-​d]​pyrimidin-​4-​amine,5,​6-​dimethyl-​N-​[1-​(phenylmethyl)​-​3-​pyrrolidinyl]​-
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
★
Size
Deutschland (EU)
USA*
Price
Qty
1mg
F413416-1mg
—
3 Auf Lager
69,33€
5mg
F413416-5mg
—
3 Auf Lager
220,32€
10mg
F413416-10mg
—
3 Auf Lager
352,22€
25mg
F413416-25mg
—
3 Auf Lager
704,52€
50mg
F413416-50mg
—
2 Auf Lager
1.129,71€
100mg
F413416-100mg
—
1 Auf Lager
1.818,69€
Enter a quantity for the sizes you want to add.
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Why this grade

≥99% 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Information

Fasnall Fasnall, a thiophenopyrimidine, is a selective fatty acid synthase (FASN) inhibitor that shows potent anti-tumor activity.


Targets

FASN

Specifications

Synonyme
Thieno[2,​3-​d]​pyrimidin-​4-​amine,5,​6-​dimethyl-​N-​[1-​(phenylmethyl)​-​3-​pyrrolidinyl]​-
Spezifikationen & Reinheit
≥99%
Biochemische und physiologische Mechanismen
Fasnall, a thiophenopyrimidine, is a selective fatty acid synthase (FASN) inhibitor that shows potent anti-tumor activity.
Storage
Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Aktionsart
INHIBITOR
Reinheit
≥99%
Namen und Kennungen
Pubchem Sid528764500
Kanonisches LächelnCC1=C(SC2=NC=NC(=C12)NC3CCN(C3)CC4=CC=CC=C4)C
IUPAC NameN-(1-benzylpyrrolidin-3-yl)-5,6-dimethylthieno[2,3-d]pyrimidin-4-amine
InChIKeyVSXRMURGJRAOCU-UHFFFAOYSA-N
INCHI1S/C19H22N4S/c1-13-14(2)24-19-17(13)18(20-12-21-19)22-16-8-9-23(11-16)10-15-6-4-3-5-7-15/h3-7,12,16H,8-11H2,1-2H3,(H,20,21,22)
Isomere SMILES CC1=C(SC2=NC=NC(=C12)NC3CCN(C3)CC4=CC=CC=C4)C
Molekulargewicht 338.47
Reaxy-Rn 31884835
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=31884835&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
KlasseThienopyrimidines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentThienopyrimidines
Alternative Parents Phenylmethylamines  Benzylamines  Secondary alkylarylamines  Aralkylamines  Aminopyrimidines and derivatives  N-alkylpyrrolidines  Imidolactams  Thiophenes  Heteroaromatic compounds  Trialkylamines  Azacyclic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Thienopyrimidine - Phenylmethylamine - Benzylamine - Aralkylamine - Secondary aliphatic/aromatic amine - Aminopyrimidine - Imidolactam - Benzenoid - N-alkylpyrrolidine - Pyrimidine - Monocyclic benzene moiety - Heteroaromatic compound - Thiophene - Pyrrolidine - Tertiary aliphatic amine - Tertiary amine - Azacycle - Secondary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as thienopyrimidines. These are heterocyclic compounds containing a thiophene ring fused to a pyrimidine ring. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

11 results found

Lot NumberCertificate TypeDatumArtikel
B2402623Certificate of AnalysisDec 28, 2023 F413416
B2402624Certificate of AnalysisDec 28, 2023 F413416
B2402625Certificate of AnalysisDec 28, 2023 F413416
B2402628Certificate of AnalysisDec 28, 2023 F413416
B2402629Certificate of AnalysisDec 28, 2023 F413416
B2402630Certificate of AnalysisDec 28, 2023 F413416
B2402631Certificate of AnalysisDec 28, 2023 F413416
B2402632Certificate of AnalysisDec 28, 2023 F413416
B2402633Certificate of AnalysisDec 28, 2023 F413416
B2402634Certificate of AnalysisDec 28, 2023 F413416
B2402635Certificate of AnalysisDec 28, 2023 F413416

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Chemische und physikalische Eigenschaften
LöslichkeitSolubility (25°C) In vitro Ethanol: 25 mg/mL (73.86 mM); DMSO: 13 mg/mL (38.4 mM); Water: Insoluble;
Molekulargewicht338.500 g/mol
XLogP34.400
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass338.157 Da
Monoisotopic Mass338.157 Da
Topological Polar Surface Area69.300 Ų
Heavy Atom Count24
Formal Charge0
Complexity414.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQs und Artikel
Citations of This Product
Referenzen
1. Chen Zixiang, Niu Kaifeng, Li Mengge, Deng Yuchun, Zhang Ji, Wei Di, Wang Jiaqi, Zhao Yongliang.  (2025)  GCLC desuccinylation regulated by oxidative stress protects human cancer cells from ferroptosis.  CELL DEATH AND DIFFERENTIATION,      [PMID:40188196] [10.1038/s41418-025-01505-8]
Lösungsrechner
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