当前位置：易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型：会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累，可浏览访问
(41-90)良好信誉积累，可接洽商谈
(91+ )优质信誉积累，可持续信赖
易推广会员：5年
工商认证 【已认证】
最后认证时间：
注册号： 【已认证】
法人代表： 【已认证】
企业类型：生产商 【已认证】
注册资金：人民币万 【已认证】
产品数：86101
参观次数：3714153
自主品牌
已选条件
-
T18332MC-VC-PABC-Aur0101；化合物 T18332MCVCPABCAur0101|||MC-VC-PABC-Aur-0101|||MC VC PABC Aur0101|||MC-VC-PABC
MC-VC-PABC-Aur0101 is a potent anticancer drug-linker conjugate designed for Antibody-Drug Conjugates (ADCs), comprising Aur0101, an auristatin microtubule inhibitor, connected through the MC-VC-PABC linker to enhance antitumor efficacy.
价 格：￥电议型 号：T18332产 地：中国大陆
-
T18304Mal-VC-PAB-ABAEP-Azonafide；化合物 T18304Mal-VC-PAB-ABAEP-Azonafide|||MalVCPABABAEPAzonafide|||Mal VC PA
Mal-VC-PAB-ABAEP-Azonafide, an ADC (antibody-drug conjugate) linker-drug conjugate, demonstrates potent antitumor activity. It incorporates Azonafide, a cytotoxin, connected through the ADC linker Mal-VC-PAB[1].
价 格：￥电议型 号：T18304产 地：中国大陆
-
T18294Mal-PEG4-VC-PAB-DMEA；化合物 T18294Mal-PEG4-VC-PAB-DMEA|||MalPEG4VCPABDMEA|||Mal PEG4 VC PAB DMEA|||Mal-
Mal-PEG4-VC-PAB-DMEA is a cleavable ADC linker that incorporates a Maleimide moiety. It is employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T18294产 地：中国大陆
-
T18292Mal-PEG4-VC-PAB-DMEA-PNU-159682；化合物 T18292Mal-PEG4-VC-PAB-DMEA-PNU159682|||MalPEG4VCPABDMEAPNU159682
Mal-PEG4-VC-PAB-DMEA-PNU-159682 is a drug-linker conjugate designed for antibody-drug conjugate (ADC) therapy. It combines the ADC linker, Mal-PEG4-VC-PAB, with the potent ADC cytotoxin, DMEA-PNU-159682. The cytotoxin, DMEA-PNU-159682, is derived from metabolites of nemorubicin (MMDX) found in liver microsomes, as well as the ADC cytotoxin PNU-159682[1].
价 格：￥电议型 号：T18292产 地：中国大陆
-
T18279Mal-PEG2-VCP-NB；化合物 T18279Mal-PEG2-VCP-NB|||Mal PEG2 VCP NB|||MalPEG2VCPNB|||Mal-PEG-2-VCP-NB；Mal-PE
Mal-PEG2-VCP-NB is a nonclaevable ADC linker containing a Maleimide group, 2-unit PEG and a VCP NB.
价 格：￥电议型 号：T18279产 地：中国大陆
-
T18278Mal-PEG2-VCP-Eribulin；化合物 T18278MalPEG2VCPEribulin|||Mal-PEG2-VCP-Eribulin|||Mal-PEG-2-VCP-Eribulin|
Mal-PEG2-VCP-Eribulin is a chemotherapeutic compound comprising an antibody-drug conjugate (ADC) linker (Mal-PEG2-VCP) and the microtubule inhibitor Eribulin[1]. This compound uniquely targets microtubules, offering a novel approach to cancer treatment. Eribulin is specifically utilized in creating targeted Eribulin-based drugs for antibody conjugates[1].
价 格：￥电议型 号：T18278产 地：中国大陆
-
T17981Fmoc-Phe-Lys(Boc)-PAB-PNP；化合物 T17981Fmoc Phe Lys(Boc) PAB PNP|||Fmoc-Phe-Lys(Boc)-PAB-PNP|||FmocPheL
Fmoc-Phe-Lys(Boc)-PAB-PNP is a cleavable antibody-drug conjugate (ADC) linker employed in the synthesis of ADCs.
价 格：￥电议型 号：T17981产 地：中国大陆
-
T17980Fmoc-Phe-Lys(Trt)-PAB-PNP；化合物 T17980Fmoc Phe Lys(Trt) PAB PNP|||Fmoc-Phe-Lys(Trt)-PAB-PNP|||FmocPheL
Fmoc-Phe-Lys(Trt)-PAB-PNP is a cleavable linker for antibody-drug conjugate (ADC) synthesis, specifically designed for use in ADC synthesis.
价 格：￥电议型 号：T17980产 地：中国大陆
-
T1796Otenabant hydrochloride；奥替那班Otenabant (CP-945598) HCl|||CP 945598 Hydrochloride|||Otenabant；奥替那班|||O
Otenabant hydrochloride (Otenabant) (CP-945598) is a competitive, high affinity, selective antagonist of the CB1 receptor (Ki: 0.7 nM).
价 格：￥电议型 号：T1796产 地：中国大陆
-
T17945Fmoc-Ala-Ala-Asn-PABC-PNP；化合物 T17945FmocAlaAlaAsnPABCPNP|||Fmoc-Ala-Ala-Asn-PABC-PNP|||Fmoc Ala Ala
Fmoc-Ala-Ala-Asn-PABC-PNP is a peptide cleavable ADC linker[1].
价 格：￥电议型 号：T17945产 地：中国大陆
-
T17817DBCO-(PEG)3-VC-PAB-MMAE；化合物 T17817DBCO (PEG)3 VC PAB MMAE|||DBCO-(PEG)3-VC-PAB-MMAE|||DBCO(PEG)3VCPA
DBCO-(PEG)3-VC-PAB-MMAE is a chemical compound where monomethyl auristatin E (MMAE), a potent tubulin inhibitor acting as a toxin payload in antibody-drug conjugates, is conjugated to a DBCO-(PEG)3-vc-PAB linker.
价 格：￥电议型 号：T17817产 地：中国大陆
-
T17816DBCO-Val-Cit-PABC-PNP；化合物 T17816DBCO Val Cit PABC PNP|||DBCOValCitPABCPNP|||DBCO-Val-Cit-PABC-PNP；DB
DBCO-Val-Cit-PABC-PNP is a cleavable linker for antibody-drug conjugate (ADC) synthesis[1].
价 格：￥电议型 号：T17816产 地：中国大陆
-
T17789DBCO-(PEG2-VC-PAB-MMAE)2；化合物 T17789DBCO-(PEG-2-VC-PAB-MMAE)2|||DBCO(PEG2VCPABMMAE)2|||DBCO-(PEG2-VC-
DBCO-(PEG2-VC-PAB-MMAE)2 consists of Monomethyl auristatin E (MMAE), a toxin payload in antibody-drug conjugate [1], conjugated to the cleavable linker DBCO-(PEG2-VC-PAB)2. MMAE, a potent tubulin inhibitor, serves as the cytotoxic component in this formulation.
价 格：￥电议型 号：T17789产 地：中国大陆
-
T17688Boc-Phe-(Alloc)Lys-PAB-PNP；化合物 T17688Boc-Phe-(Alloc)Lys-PAB-PNP|||BocPhe(Alloc)LysPABPNP|||Boc Phe (
Boc-Phe-(Alloc)Lys-PAB-PNP serves as a cleavable linker in the synthesis of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T17688产 地：中国大陆
-
T17315(±)-CPSI-1306；化合物cpsi-1306cpsi-1306|||2-(3-(2,4-Difluorophenyl)-4,5-dihydroisoxazol-5-yl)-1-morpholi
(±)-CPSI-1306 (2-(3-(2,4-Difluorophenyl)-4,5-dihydroisoxazol-5-yl)-1-morpholinoethan-1-one) is a macrophage migration inhibitory factor (MIF) antagonist and can be used in studies about non-insulin-dependent diabetes mellitus (NIDDM) and the prevention of the deleterious cutaneous effects of acute and chronic UVB exposure.
价 格：￥电议型 号：T17315产 地：中国大陆
-
T17304α-Tocopherol phosphateα-生育酚磷酸盐vitamin E phosphate|||TocP|||alpha-Tocopherol phosphate|||α-生育酚磷酸盐
α-Tocopherol phosphate is the compound demonstrating the highest vitamin E activity.
价 格：￥电议型 号：T17304产 地：中国大陆
-
T17036Tenidap；替尼达普CP-66248；CP-66248
Tenidap (CP-66248) is a selective COX-1 and SLC26A3 inhibitor with anti-inflammatory, analgesic, and anti-rheumatic activities.
价 格：￥电议型 号：T17036产 地：中国大陆
-
T17018TCPOBOP；化合物TCPOBOPTCPOBOP
TCPOBOP is a constitutive androstane receptor agonist that induces robust hepatocyte proliferation and hepatomegaly. TCPOBOP decreases Fas-induced murine liver injury by altering Bcl-2 proteins.
价 格：￥电议型 号：T17018产 地：中国大陆
-
T1657Varenicline Tartrate；酒石酸伐尼克兰Champix tartrate|||Chantix tartrate|||CP 526555-18；Champix tartrate|||酒石
Varenicline Tartrate (CP 526555-18) is a benzazepine derivative that functions as an ALPHA4/BETA2 NICOTINIC RECEPTOR partial agonist. It is used for SMOKING CESSATION.
价 格：￥电议型 号：T1657产 地：中国大陆
-
T16541Pirolate；化合物 T16541CP-32387；CP-32387
Pirolate is a receptor of histamine H1.
价 格：￥电议型 号：T16541产 地：中国大陆
