Ferroptosis
Ferroptosis is a unique iron-dependent form of nonapoptotic cell death. It is triggered by oncogenic RAS-selective lethal small molecule erastin. Acitvation of ferroptosis lead to nonapoptotic destruction of cancer cells.
Products Related to Ferroptosis(211)
- GC47123Coumarin-Quinone ConjugateCAS: 2741190-31-6Purity: >95.00%
A fluorescent substrate for NADH:ubiquinone oxidoreductases
- GC47870Pantothenate Kinase InhibitorCAS: 902614-04-4Purity: >95.00%
A reversible inhibitor of pantothenate kinase
- GC48059Rosiglitazone-d3CAS: 1132641-22-5Purity: >99.00%
An internal standard for the quantification of rosiglitazone
- GC49058Pentetic acid (DTPA)CAS: 67-43-6Purity: >98.00%
Pentetic acid (DTPA)은 강력한 아미노폴리카복실산 킬레이트제로 EDTA와 유사한 구조를 가지고 있다.
- GC49308UngeremineCAS: 2121-12-2Purity: >98.00%
A betaine-type alkaloid with diverse biological activities
- GC497301-Stearoyl-2-15(S)-HETE-sn-glycero-3-PE-d11Purity: >99.00%
An internal standard for the quantification of 1-stearoyl-2-15(S)-HETE- sn -glycero-3-PE
- GC50345Liproxstatin-1 hydrochlorideCAS: 2250025-95-5Purity: >98%
Liproxstatin-1 염산염은 강력한 ferroptosis 억제제이며 ferroptosis 세포 사멸을 억제합니다(IC50=22nM).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC45793 | IM-93 | 1173657-73-2 | >98.00% | |
IM-93은 세포 사멸 억제에 대해 0.45μM의 IC50으로 ferroptosis와 NETosis를 억제합니다. | ||||
| GC45820 | Balsalazide-d4 | - | >99.00% | |
Balsalazide-d4는 Balsalazide로 표시된 중수소입니다. | ||||
| GC45928 | iFSP1 | 150651-39-1 | >99.50% | |
iFSP1은 글루타티온 비의존 철사 억제 단백질1(FSP1)의 강력한 억제제로 EC 50 값이 103nM이다. | ||||
| GC45995 | DO264 | 2301866-59-9 | >98.50% | |
An ABHD12 inhibitor | ||||
| GC46352 | (S)-DO271 | 2301865-01-8 | >98.00% | |
An inactive control for DO264 | ||||
| GC47065 | CAY10773 | 1648546-79-5 | >98.00% | |
A derivative of sorafenib | ||||
| GC47123 | Coumarin-Quinone Conjugate | 2741190-31-6 | >95.00% | |
A fluorescent substrate for NADH:ubiquinone oxidoreductases | ||||
| GC47477 | JKE-1674 | 2421119-60-8 | >98.00% | |
JKE-1674는 경구 활성 글루타티온 퍼옥시다제 4(GPX4) 억제제이자 GPX4 억제제 ML-210의 활성 대사 산물입니다. JKE-1674, 니트로이속사졸 고리가 α-니트로케톡심으로 대체된 ML-210의 유사체. JKE-1674는 니트릴 산화물 JKE-1777로 변환할 수 있습니다. JKE-1674는 ML-210과 동일한 방식으로 LOX-IMVI 세포를 죽이고 ferroptosis 억제제에 의해 완전히 구제됩니다. | ||||
| GC47478 | JKE-1716 | 2421118-05-8 | >98.00% | |
JKE-1716은 강력하고 선택적인 니트로산 함유 GPX4 억제제입니다. | ||||
| GC47870 | Pantothenate Kinase Inhibitor | 902614-04-4 | >95.00% | |
A reversible inhibitor of pantothenate kinase | ||||
| GC48029 | RC363 | 2584411-86-7 | >98.00% | |
An inhibitor of ferroptosis | ||||
| GC48030 | RC574 | 2584411-87-8 | >98.00% | |
An inhibitor of ferroptosis | ||||
| GC48059 | Rosiglitazone-d3 | 1132641-22-5 | >99.00% | |
An internal standard for the quantification of rosiglitazone | ||||
| GC48650 | DTUN | - | >95.00% | |
A lipophilic hyponitrite radical initiator | ||||
| GC48954 | CP21 | 30652-12-1 | >98.00% | |
An iron chelator | ||||
| GC49034 | 1(R)-(Trifluoromethyl)oleyl alcohol | 2644636-20-2 | >95.00% | |
An oleic acid analog | ||||
| GC49058 | Pentetic acid (DTPA) | 67-43-6 | >98.00% | |
Pentetic acid (DTPA)은 강력한 아미노폴리카복실산 킬레이트제로 EDTA와 유사한 구조를 가지고 있다. | ||||
| GC49308 | Ungeremine | 2121-12-2 | >98.00% | |
A betaine-type alkaloid with diverse biological activities | ||||
| GC49454 | Complex 3 | 2480150-28-3 | >90.00% | |
A fluorescent copper complex with anticancer activity | ||||
| GC49560 | L6H21 | 24533-47-9 | >98.00% | |
Chalcone 유도체인 L6H21은 경구 활성, 강력하고 특이적인 골수 분화 2(MD-2) 억제제입니다. | ||||
| GC49691 | PSP | 3030735-86-2 | >98.00% | |
A two-photon fluorescent probe for H 2 S n | ||||
| GC49730 | 1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PE-d11 | - | >99.00% | |
An internal standard for the quantification of 1-stearoyl-2-15(S)-HETE- sn -glycero-3-PE | ||||
| GC49868 | D-α-Tocopheryl Quinone | 7559-04-8 | >98.00% | |
An oxidative metabolite of vitamin E | ||||
| GC50345 | Liproxstatin-1 hydrochloride | 2250025-95-5 | >98% | |
Liproxstatin-1 염산염은 강력한 ferroptosis 억제제이며 ferroptosis 세포 사멸을 억제합니다(IC50=22nM). | ||||
