DS18561882 - 10mM in DMSO , CAS No.2227149-22-4

CAS: 2227149-22-4 Cat. No.: D655105 분자식: C28H31F3N4O6S 분자량: 608.63 PubChem CID: 139486677
주문 가능
GRADE & PURITY 10mM in DMSO
Storage
Argon charged,Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
USA
독일 (EU)*
Price
Qty
1ml
D655105-1ml
주문제작 · 8~12주
US$992.90
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Store at -80°C Ships Dry ice packs + Cold packs 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

DS18561882 is a highly potent, isozyme-selective methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) inhibitor with an IC 50 value of 0.0063 μM. DS18561882 also has inhibitory effect on MTHFD1 ( IC 50 =0.57 μM). DS18561882 exhibits a good oral pharmacokinetic profile

In Vitro

DS18561882 (0-150 nM) gives the lowest GI 50 value (140 nM) against the MDA-MB-231 cell line. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

DS18561882 (oral administration; 30, 100 or 300 mg/kg; twice daily) inhibits tumor growth inhibition with a dose-dependent manner, the tumor is completely inhibited (TGI: 67%) at the dose of 300 mg/kg in mice . DS18561882 (oral administration; 10, 30, 100, or 300 mg/kg) has a good oral pharmacokinetic profile, including ACU (64.6, 264, 726 μg.h/ml ); C max (11.4, 56.5, 90.1 μg/ml); t 1/2 (2.21, 2.16, 2.32 hours) for 30 mg/kg; 100mg/kg; 200 mg/kg, respectively . DS18561882 is suspended in a 0.5% (w/v) methyl cellulose 400 solution in this article . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Five week old female BALB/cAJcl-nu/nu mice with MDA-MB-231 luc tumor cells (4 × 10 6 cells/mouse) Dosage: 30, 100 or 300 mg/kg Administration: Oral administration; 30, 100 or 300 mg/kg; twice daily; until day 11 Result: Suppressed tumor growth in a dose-dependent manner.

IC50& Target:IC50: 0.0063 μM (MTHFD2),0.57 μM (MTHFD1)

Specifications

사양 및 순도
10mM in DMSO
생화학 및 생리적 메커니즘
DS18561882 is a highly potent, isozyme-selective methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) inhibitor with an IC 50 value of 0.0063 μM. DS18561882 also has inhibitory effect on MTHFD1 ( IC 50 =0.57 μM). DS18561882 exhibits a good oral pharmacokine
보관 조건
Argon charged,Store at -80°C
배송
Dry ice packs + Cold packs
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이름과 식별자
이성체 SMILES C[C@H]1CN(CCN1C)C2=C(C3=C(C=C2)C4=C(CN(CC4)C(=O)C5=CC(=C(C=C5)NS(=O)(=O)C)OC(F)(F)F)C(=O)O3)C
PubChem CID 139486677
분자량 608.63

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

관련 대상(인간)
MTHFD1 Tchem C-1-tetrahydrofolate synthase, cytoplasmic (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MTHFD2 Tchem Bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
인증서(CoA, COO, BSE/TSE 및 분석 차트)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
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