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Search Results for " 240 "
Targets Recommended: Others

82

抑制剂 & 化合物

3

天然产物

6

重组蛋白

2

同位素标记化合物

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Cat. No. Product Name Target Signaling Pathways
T67842 ERG240

EGR240

Others Others
ERG240 是支链氨基酸转氨酶 1 (BCAT1) 抑制剂。ERG240 有潜力用于癌症、类风湿性关节炎和骨病相关研究。
T29067 Upacicalcet

PLS-240,SK-1403,AJT-240

Calcium Channel Membrane transporter/Ion channel; Metabolism
Upacicalcet (AJT-240) 是一种静脉内拟钙剂,是一种可用于人血液透析的 SHPT, 通过直接作用于甲状旁腺细胞膜钙敏感受体来抑制过量的甲状旁腺激素 (PTH) 分泌,从而降低血液中的 PTH 水平。 3 Upacicalcet 是钙敏感受体的正变构调节剂,可预防大鼠腺嘌呤诱导的继发性甲状旁腺功能亢进模型中的血管钙化和骨骼疾病。
T3535 ML240

p97 Ubiquitination
ML240 是一种选择性的 ATP 竞争性 p97 抑制剂,IC50值为 100 nM。
T29236 ZTZ240

ZTZ 240,ZTZ-240

Others Others
ZTZ240, a KCNQ2 K+ channel activator, offers a new target to treat hyperexcitability disorders.
T30666 C.I. Food Blue 1-aluminum lake

EINECS 240-589-3,Indigotine-aluminum lake,Acid Blue 74-aluminum lake,Pigment Blue 63

Others Others
C.I. Food Blue 1-aluminum lake is a type of colorant.
T40495 Elastase from porcine pancreas

弹性蛋白酶,EC 3.2.1.35

Others Others
Elastase from porcine pancreas 由 240 个氨基酸残基组成,是一种丝氨酸蛋白酶,可以水解蛋白质和多肽。它可诱发仓鼠气肿。
T61122 ZINC12409120

R-4584

ERK MAPK
ZINC12409120 (R-4584) 是一种具有选择性的 ERK 抑制剂。ZINC12409120 对ERK具有抑制作用,IC50 为 5.0 μM。ZINC12409120 通过干扰 FGF23:α-Klotho 的相互作用而抑制 ERK 活性。
T14501 BAY-2402234

Dehydrogenase; DNA/RNA Synthesis Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism
BAY-2402234 是一种选择性二氢乳清酸脱氢酶的抑制剂,可研究骨髓恶性肿瘤。
T2081 LY2409881 trihydrochloride

LY2409881

Apoptosis; IκB/IKK Apoptosis; NF-κB
LY2409881 trihydrochloride 是一种新型 IKK2 特异性抑制剂,IC50为 30 nM。
T5048 SSR240612

Bradykinin Receptor GPCR/G Protein
SSR240612 是口服有活性的非肽类缓激肽 B1 (bradykinin B1) 受体特异性拮抗剂。
TQ0139 VU 0240551

N-(4-Methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide,VU0240551-2-D4

Potassium Channel; Calcium Channel; HER Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Metabolism; Tyrosine Kinase/Adaptors
VU 0240551 是神经元 K-Cl 协同转运蛋白 KCC2 抑制剂的特异性拮抗剂,IC50 为 560 nM。 VU 0240551 抑制 L 型钙通道和 hERG。
T2248 AS-605240

5-(6-喹噁啉yl亚甲基)-2,4-噻唑烷二酮,AS 605240

PI3K; Autophagy Autophagy; PI3K/Akt/mTOR signaling
AS-605240 是一种有效且特异性的 PI3Kγ 抑制剂,IC50值为 8 nM,Ki 值为 7.8 nM。
T13248 UK-240455

NMDAR; iGluR Membrane transporter/Ion channel; Neuroscience
UK-240455是一种有效的且具有选择性的 N-甲基 D-天冬氨酸 (NMDA) 甘氨酸受体拮抗剂,具有神经保护作用和改善帕金森病模型的运动的功能,是治疗帕金森病的潜在候选化合物。
TP1127L1 Nemifitide acetate(173240-15-8 free base)

INN 00835 acetate

5-HT Receptor GPCR/G Protein; Neuroscience
Nemifitide acetate(173240-15-8 free base) (INN 00835 acetate) 是一种合成的五肽抗抑郁药,具有快速起效的潜力。它是黑色素细胞抑制因子 (MIF) 的肽类似物。
T61702 SRI-37240

CFTR Membrane transporter/Ion channel
SRI-37240是一种有效的提前终止密码子 (PTCs) 抑制剂,具有通读活性的,可诱导终止密码子处的长时间停顿,抑制与囊性纤维化相关的 PTC。SRI-37240 可用于研究与PTC 相关的疾病。
T32490 L-161240

L-161,240

Antibacterial Microbiology/Virology
L-161240 是一种与脂质A生物合成有关的抗菌剂,在DEACET测定IC50值为 30 nM,并且对野生型大肠杆菌的MIC值为1-3μg/ mL。
T16889 SJ572403

SJ403

Others Others
SJ572403 是一种无序蛋白 p27 的抑制剂,对于 p27-KID 的 D2 亚结构域内的特定区域的 Kd 为 2.2 mM。 SJ572403 可用于研究具有内在无序蛋白质的疾病。
T15802 LY2183240

FAAH; Autophagy Autophagy; Metabolism; Neuroscience
LY2183240 是大麻素摄取阻滞剂。它是内源性大麻素降解酶脂肪酸酰胺水解酶的有效共价抑制剂。它抑制脂肪酸酰胺水解酶 (FAAH) 活性,IC50 为12.4 nM。它也抑制其他几种脑丝氨酸水解酶,对 MAG 脂肪酶、bh6 和 KIAA1363 的 IC50分别为 5.3、0.09 和 8.2 nM。
T19429 MK-6240

Others Others
MK-6240 is a tau positron emission tomography (PET) tracer for neurofibrillary tangles (NFTs). MK-6240 exhibits high specificity and selectivity for binding to NFTs.
T16678 PSN632408

Others Others
PSN632408 is an optimized agonist of GPR119 receptors that display similar potency to OEA at both recombinant mouse and human GPR119 receptors (EC50: 5.6 and 7.9 uM, respectively).
T25885 NSC12404

CID 224134,CID224134,CID-224134,NSC 12404,NSC-12404

Others Others
NSC-12404 is a selective non-lipid LPA2/3 agonist.
T29124 VU0240382

VU-0240382,VU 0240382

Others Others
VU0240382 is a selective positive allosteric modulators of metabotropic glutamate receptor subtype 5.
T28005 MDL-100240

Others Others
MDL-100240 is a dual inhibitor of angiotensin-converting enzyme (ACE) and neprilysin with a balanced activity. MDL 100240 shows an impressive effectiveness both in preventing and in regressing hypertension-induced vascular remodeling and cardiac hypertrop
T30091 AP-22408

UNII-3U3L5QR4KV,AC1L9I7C,AP22408,CC1

Others Others
AP-22408 is an inhibitor of SRC tyrosine kinase.
T13342L WIN site inhibitor 1 TFA (2407457-36-5 free base)

WIN site inhibitor 1 TFA

Others Others
WIN site inhibitor 1 TFA is a WIN site of chromatin-associated WD repeat-containing protein 5 (WDR5) inhibitor (Kd: 0.1 nM).
T25234 CH5447240

CH 5447240,CH-5447240

Others Others
CH5447240 is an effective Human Parathyroid Hormone Receptor 1 (hPTHR1) Agonist for the treatment of Hypoparathyroidism. CH5447240 showed a potent in vitro hPTHR1 agonist effect (EC20: 3.0 nM; EC50: 12 nM). It showed 55% oral bioavailability and a signifi
T28243 Ono 6240

Ono-6240,Ono6240

Others Others
Ono 6240 is an antagonist of platelet-activating factor. Ono 6240 prevents airway eosinophilia by inhibiting production of IL-2 and IL-5.
T26096 RJR-2403 oxalate

RJR 2403 oxalate,Rivanicline oxalate,TC-2403,Metanicotine

Others Others
RJR-2403 oxalate is a highly selective agonist of α4β2 subtype nicotinic receptor.
T34539 SB 414240

SB-414240,SB414240

Others Others
SB 414240 is a bioactive chemical.
T22896 L-655,240

Others Others
L-655,240 is a thromboxane A2/prostaglandin endoperoxide receptor antagonist.
T30662 C.I. 74240

NSC 324570,NSC-324570,NSC324570

C.I. 74240 is a copper-containing dye used as a gelling agent for lubricants, for staining of bacteria and for the dyeing of histiocytes and fibroblasts in vivo.
T34475 S24014

S-24014,S 24014

Others Others
S24014 is a bioactive chemical.
T36246 SJF 8240

Others Others
c-MET degrader. Comprises MET inhibitor foretinib (GSK 1363089; Cat. No. 6056) joined by a linker to a von Hippel-Lindau (VHL) recruiting ligand. Degrades c-MET within 6 hours in vitro. Inhibits agonist-driven AKT phosphorylation and GTL16 cell proliferation (IC50 = 66.7 nM). Also degrades exon-14-deleted c-MET in Hs746T cells.
T41101 LY2409881

LY2409881

Others Others
LY2409881 is a selective IκB kinase β ( IKK2 ) inhibitor with an IC 50 of 30 nM.
T11545L hDDAH-1-IN-2 sulfate (2408834-77-3 free base)

hDDAH-1-IN-2 sulfate

Others Others
hDDAH-1-IN-2 sulfate is an orally active human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) inhibitor.
T30857 CGS 24012

CGS24012,CGS-24012

Others Others
CGS 24012 is a bioactive chemical.
T28530 RG-102240

RG102240,RG 102240

Others Others
RG-102240 acts as a transcription inducer for use in induceable gene expression systems.
T23755 AS1468240

AS 1468240,AS-1468240

Others Others
AS1468240 is a factor Xa inhibitor. It has significant oral anticoagulant activity.
T29724 AGN 192240

AGN-192240,AGN192240

Others Others
AGN 192240 is a biochemical.
T27668 JNJ-2408068

R170591,R 170591,HE066500,R-170591,HE-066500,HE 066500

Others Others
JNJ-2408068 is an inhibitor of respiratory syncytial virus (RSV). JNJ-2408068 exhibited potent antiviral activity with EC50 of 2.1 nM. A similar inhibitory effect was observed in a RSV-mediated cell fusion assay (EC50= 0.9 nM). JNJ-2408068 interferes with
T37558 Necrostatin-5

Nec-5

RIP kinase; Necroptosis Apoptosis; NF-κB
Necrostatin-5 (Nec-5)是一种RIP1激酶的选择性抑制剂,也是一种细胞坏死抑制剂,可防止TNF-α处理的fadd 缺陷Jurkat 细胞死亡,EC50值为240 nM。
T9075 BDP-13176

Others Others
BDP-13176 是fascin 1抑制剂,Kd=90 nM,IC50=240 nM。它具有成为抗转移剂的潜力。
T21938 AS-041164

PI3K PI3K/Akt/mTOR signaling
AS-041164 是选择性的,具有口服活性的PI3Kγ亚型抑制剂,IC50=70 nM。它对 PI3Kα (IC50:240 μM),PI3Kβ (IC50:1.45 μM) 和 PI3Kδ (IC50:1.70 μM) 的活性较低。它具有抗炎活性。
T40236 ART812

ART812

DNA/RNA Synthesis Cell Cycle/Checkpoint; DNA Damage/DNA Repair
ART812 is an orally active inhibitor of DNA polymerase Polθ, possessing an IC50 value of 7.6 nM. Additionally, ART812 exhibits a cell-based microhomology-mediated end joining (MMEJ) IC50 value of 240 nM.
T6726 VU0361737

ML-128,VU 0361737

GluR Neuroscience
VU0361737 (ML-128) 是一种高效选择性的,中枢神经系统渗透性的代谢型谷氨酸受体 4(mGluR4)正变构调节剂,对人类和大鼠 mGluR4作用的EC50值分别为 240 和 110 nM。它具有神经保护作用,有用于帕金森氏病的研究潜力。
T7648 HA-100

Myosin; PKA; PKC Chromatin/Epigenetic; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
HA-100 是蛋白激酶和ROCK 抑制剂,抑制PKG,PKA,PKC 和MLC 激酶的IC50值分别为 4、8、12 和 240 μM。
T6644 Rolipram

SB 95952,ZK 62711,咯利普兰,(R,S)-Rolipram

HIV Protease; Antibacterial; PDE Metabolism; Microbiology/Virology; Proteases/Proteasome
Rolipram (SB 95952) 是一种磷酸二酯酶 PDE4的选择性抑制剂,抑制 PDE4A,PDE4B 和 PDE4D 的 IC50分别为 3 nM,130 nM 和 240 nM。
T6036 Brivanib

BMS-540215,布立尼布

EGFR; VEGFR; FGFR; Autophagy Angiogenesis; Autophagy; JAK/STAT signaling; Tyrosine Kinase/Adaptors
Brivanib (BMS-540215) 是一种针对 VEGFR2 的 ATP 竞争性抑制剂,IC50 为 25 nM。它对 VEGFR-1 和 FGFR-1 具有中等效力,对 VEGFR2 的选择性是对 PDGFR-β 的 240 倍。
T6787 BIO-acetoxime

BIA,GSK-3 Inhibitor X

Apoptosis; GSK-3; HSV Apoptosis; Microbiology/Virology; PI3K/Akt/mTOR signaling; Stem Cells
BIO-acetoxime (GSK-3 Inhibitor X) 是一种 GSK3α/β 抑制剂,IC50值均为 10 nM,具有抗惊厥和抗感染作用。
T8477 IQ-3

JNK MAPK
IQ3 是c-JNK 家族选择性抑制剂,对JNK3 的选择性更好。它对JNK1、JNK2 和 JNK3 的Kd 值分别为0.24 μM、0.29 μM 和 0.066 μM。

化合物

ERG240
Cat.No: T67842
Synonym: EGR240
Target: Others
Upacicalcet
Cat.No: T29067
Synonym: PLS-240,SK-1403,AJT-240
Target: Calcium Channel
ML240
Cat.No: T3535
Synonym:
Target: p97
ZTZ240
Cat.No: T29236
Synonym: ZTZ 240,ZTZ-240
Target: Others
C.I. Food Blue 1-aluminum lake
Cat.No: T30666
Synonym: EINECS 240-589-3,Indigotine-aluminum lake,Acid Blue 74-aluminum lake,Pigment Blue 63
Target: Others
Elastase from porcine pancreas
Cat.No: T40495
Synonym: 弹性蛋白酶,EC 3.2.1.35
Target: Others
ZINC12409120
Cat.No: T61122
Synonym: R-4584
Target: ERK
BAY-2402234
Cat.No: T14501
Synonym:
Target: Dehydrogenase, DNA/RNA Synthesis
LY2409881 trihydrochloride
Cat.No: T2081
Synonym: LY2409881
Target: Apoptosis, IκB/IKK
SSR240612
Cat.No: T5048
Synonym:
Target: Bradykinin Receptor
VU 0240551
Cat.No: TQ0139
Synonym: N-(4-Methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide,VU0240551-2-D4
Target: Potassium Channel, Calcium Channel, HER
AS-605240
Cat.No: T2248
Synonym: 5-(6-喹噁啉yl亚甲基)-2,4-噻唑烷二酮,AS 605240
Target: PI3K, Autophagy
UK-240455
Cat.No: T13248
Synonym:
Target: NMDAR, iGluR
Nemifitide acetate(173240-15-8 free base)
Cat.No: TP1127L1
Synonym: INN 00835 acetate
Target: 5-HT Receptor
SRI-37240
Cat.No: T61702
Synonym:
Target: CFTR
L-161240
Cat.No: T32490
Synonym: L-161,240
Target: Antibacterial
SJ572403
Cat.No: T16889
Synonym: SJ403
Target: Others
LY2183240
Cat.No: T15802
Synonym:
Target: FAAH, Autophagy
MK-6240
Cat.No: T19429
Synonym:
Target: Others
PSN632408
Cat.No: T16678
Synonym:
Target: Others
NSC12404
Cat.No: T25885
Synonym: CID 224134,CID224134,CID-224134,NSC 12404,NSC-12404
Target: Others
VU0240382
Cat.No: T29124
Synonym: VU-0240382,VU 0240382
Target: Others
MDL-100240
Cat.No: T28005
Synonym:
Target: Others
AP-22408
Cat.No: T30091
Synonym: UNII-3U3L5QR4KV,AC1L9I7C,AP22408,CC1
Target: Others
WIN site inhibitor 1 TFA (2407457-36-5 free base)
Cat.No: T13342L
Synonym: WIN site inhibitor 1 TFA
Target: Others
CH5447240
Cat.No: T25234
Synonym: CH 5447240,CH-5447240
Target: Others
Ono 6240
Cat.No: T28243
Synonym: Ono-6240,Ono6240
Target: Others
RJR-2403 oxalate
Cat.No: T26096
Synonym: RJR 2403 oxalate,Rivanicline oxalate,TC-2403,Metanicotine
Target: Others
SB 414240
Cat.No: T34539
Synonym: SB-414240,SB414240
Target: Others
L-655,240
Cat.No: T22896
Synonym:
Target: Others
C.I. 74240
Cat.No: T30662
Synonym: NSC 324570,NSC-324570,NSC324570
Target:
S24014
Cat.No: T34475
Synonym: S-24014,S 24014
Target: Others
SJF 8240
Cat.No: T36246
Synonym:
Target: Others
LY2409881
Cat.No: T41101
Synonym: LY2409881
Target: Others
hDDAH-1-IN-2 sulfate (2408834-77-3 free base)
Cat.No: T11545L
Synonym: hDDAH-1-IN-2 sulfate
Target: Others
CGS 24012
Cat.No: T30857
Synonym: CGS24012,CGS-24012
Target: Others
RG-102240
Cat.No: T28530
Synonym: RG102240,RG 102240
Target: Others
AS1468240
Cat.No: T23755
Synonym: AS 1468240,AS-1468240
Target: Others
AGN 192240
Cat.No: T29724
Synonym: AGN-192240,AGN192240
Target: Others
JNJ-2408068
Cat.No: T27668
Synonym: R170591,R 170591,HE066500,R-170591,HE-066500,HE 066500
Target: Others
Necrostatin-5
Cat.No: T37558
Synonym: Nec-5
Target: RIP kinase, Necroptosis
BDP-13176
Cat.No: T9075
Synonym:
Target: Others
AS-041164
Cat.No: T21938
Synonym:
Target: PI3K
ART812
Cat.No: T40236
Synonym: ART812
Target: DNA/RNA Synthesis
VU0361737
Cat.No: T6726
Synonym: ML-128,VU 0361737
Target: GluR
HA-100
Cat.No: T7648
Synonym:
Target: Myosin, PKA, PKC
Rolipram
Cat.No: T6644
Synonym: SB 95952,ZK 62711,咯利普兰,(R,S)-Rolipram
Target: HIV Protease, Antibacterial, PDE
Brivanib
Cat.No: T6036
Synonym: BMS-540215,布立尼布
Target: EGFR, VEGFR, FGFR, Autophagy
BIO-acetoxime
Cat.No: T6787
Synonym: BIA,GSK-3 Inhibitor X
Target: Apoptosis, GSK-3, HSV
IQ-3
Cat.No: T8477
Synonym:
Target: JNK
Cat. No. Product Name Target Signaling Pathways
T4760 KSD 2405

3-羟基苯甲醇,3-Hydroxybenzyl alcohol

Others; Endogenous Metabolite Metabolism; Others
KSD 2405 (3-Hydroxybenzyl alcohol) 是内源性代谢产物的一种。
TN6414 Plantanone B

Plantanone C exhibited moderate antioxidant activity against DPPH radical scavenging activity,with an IC50 value of 240. 2 μmol·L~(-1).
T38015 Herquline A

Others Others
Herquline A is an alkaloid fungal metabolite originally isolated from P. herquei. It inhibits cell death induced by influenza A strain A/PR/8/34 in MDCK cells with an IC50 value of 10 μg/ml and inhibits viral replication in a plaque assay in a concentration-dependent manner. Herquline A also inhibits platelet aggregation induced by ADP and platelet-activating factor (PAF) in vitro (IC50s = 180 and 240 μM, respectively).

天然产物

KSD 2405
Cat.No: T4760
Synonym: 3-羟基苯甲醇,3-Hydroxybenzyl alcohol
Target: Others, Endogenous Metabolite
Plantanone B
Cat.No: TN6414
Synonym:
Target:
Herquline A
Cat.No: T38015
Synonym:
Target: Others
Cat. No. Product Name Species Expression System
TMPY-04237 Neuregulin-1/NRG1 Protein, Canine, Recombinant (aa 176-240, His)

neuregulin 1

Canine HEK293 Cells
Neuregulin-1/NRG1 Protein, Canine, Recombinant (aa 176-240, His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 9.7 kDa.
TMPY-03903 Neuregulin-1/NRG1 Protein, Canine, Recombinant (aa 19-240, His)

neuregulin 1

Canine HEK293 Cells
Neuregulin-1/NRG1 Protein, Canine, Recombinant (aa 19-240, His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 25.5 kDa and the accession number is XP_858147.1.
TMPK-01491 HLA-A*02:01&B2M&HBV (FLLTRILTI) Monomer Protein, Human, MHC (His & Avi), Biotinylated

MHC,HBV,Hepatitis B virus

Human HEK293 Cells
Hepatitis B virus (HBV), is the leading cause of liver diseases infecting an estimated 240 million persons worldwide. The HBV prevalence rates are variables between different countries, with an high level of endemicity in the south-eastern part of Europe. Seven main HBV-D subgenotypes have been described until now (D1-D7).
TMPK-01501 HLA-A*02:01&B2M&HBV (FLLTRILTI) Tetramer Protein, Human, MHC (His & Avi)

MHC,Hepatitis B virus,HBV

Human HEK293 Cells
Hepatitis B virus (HBV), is the leading cause of liver diseases infecting an estimated 240 million persons worldwide. The HBV prevalence rates are variables between different countries, with an high level of endemicity in the south-eastern part of Europe. Seven main HBV-D subgenotypes have been described until now (D1-D7).
TMPK-01492 HLA-A*02:01&B2M&HBV (FLLTRILTI) Monomer Protein, Human, MHC (His & Avi)

Hepatitis B virus,HBV,MHC

Human HEK293 Cells
Hepatitis B virus (HBV), is the leading cause of liver diseases infecting an estimated 240 million persons worldwide. The HBV prevalence rates are variables between different countries, with an high level of endemicity in the south-eastern part of Europe. Seven main HBV-D subgenotypes have been described until now (D1-D7).
TMPH-00895 Human adenovirus B serotype 3 Hexon protein (His & Myc)

Hexon protein,Protein II,L3

HAdV-3 E. coli
Major capsid protein that self-associates to form 240 hexon trimers, each in the shape of a hexagon, building most of the pseudo T=25 capsid. Assembled into trimeric units with the help of the chaperone shutoff protein. Transported by pre-protein VI to the nucleus where it associates with other structural proteins to form an empty capsid. Might be involved, through its interaction with host dyneins, in the intracellular microtubule-dependent transport of incoming viral capsid to the nucleus. Hum...

重组蛋白

Neuregulin-1/NRG1 Protein, Canine, Recombinant (aa 176-240, His)
Cat.No: TMPY-04237
Species: Canine
Expression System: HEK293 Cells
Neuregulin-1/NRG1 Protein, Canine, Recombinant (aa 19-240, His)
Cat.No: TMPY-03903
Species: Canine
Expression System: HEK293 Cells
HLA-A*02:01&B2M&HBV (FLLTRILTI) Monomer Protein, Human, MHC (His & Avi), Biotinylated
Cat.No: TMPK-01491
Species: Human
Expression System: HEK293 Cells
HLA-A*02:01&B2M&HBV (FLLTRILTI) Tetramer Protein, Human, MHC (His & Avi)
Cat.No: TMPK-01501
Species: Human
Expression System: HEK293 Cells
HLA-A*02:01&B2M&HBV (FLLTRILTI) Monomer Protein, Human, MHC (His & Avi)
Cat.No: TMPK-01492
Species: Human
Expression System: HEK293 Cells
Human adenovirus B serotype 3 Hexon protein (His & Myc)
Cat.No: TMPH-00895
Species: HAdV-3
Expression System: E. coli
Cat. No. Product Name Target Signaling Pathways
TMID-0031 WXG02403-d9

(S)-benzyl 2-((tert-butoxycarbonyl)amino)-3,3-dimethylbutanoate-d9

WXG02403-d9 是 WXG02403 的氘代化合物。WXG02403 的 CAS 号为 154092-61-2。
TMIH-0124 Brivanib Alaninate-d4

Brivanib Alaninate-d4 是 Brivanib Alaninate 的氘代化合物。Brivanib Alaninate 的 CAS 号为 649735-63-7。Brivanib alaninate 是一种血管内皮生长因子受体 2 (VEGFR2) 抑制剂的丙氨酸盐,IC50值为 25 nM,具有潜在的抗肿瘤活性。它对 VEGFR1 和 FGFR1 适度抑制,对 VEGFR2 的选择性是对 PDGFRβ 的 240 倍。

同位素标记化合物

WXG02403-d9
Cat.No: TMID-0031
Synonym: (S)-benzyl 2-((tert-butoxycarbonyl)amino)-3,3-dimethylbutanoate-d9
Target:
Brivanib Alaninate-d4
Cat.No: TMIH-0124
Synonym:
Target:
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