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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T60908 |
SARM1-IN-2
|
Others | Others |
SARM1-IN-2 是一种有效的 SARM1 抑制剂,可用于研究代谢系统和神经系统相关疾病。 | |||
T26539 |
AC-262536
AC262536,4-(3-内型-羟基-8-氮杂双环[3.2.1]辛烷-8-基)萘-1-甲腈 |
Androgen Receptor | Endocrinology/Hormones |
AC-262536 是非甾体雄激素受体选择性调节剂,具有有益的合成代谢作用。它可以强效激动雄激素受体,亲和力为1-10 nM。 | |||
T28663 |
Sarmustine
NSC-364432,SarCNU,Sarcosinamide,NSC 364432,NSC364432 |
||
Sarmustine (SarCNU) 是一种具有抗癌活性的烷化剂,通过 p53 依赖性和 p53 非依赖性途径抑制前列腺癌细胞的生长。Sarmustine 在体外介导 P140K 甲基鸟嘌呤-DNA-甲基转移酶转导的人 CD34(+)细胞的选择。 | |||
T16844 |
Sarmazenil
R-154513,Ro 15-3505 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Sarmazenil (Ro 15-3505) 是苯二氮卓受体部分反向激动剂,具有促惊厥作用,可用于研究慢性肝性脑病 (HE) 。 | |||
T4358 |
Vosilasarm
Testolone,RAD140 |
Androgen Receptor | Endocrinology/Hormones |
Testolone 是一种有效的、非甾体的、具有口服活性的、选择性雄激素受体调节剂 (SARM),Ki 为 7 nM。它对雄激素受体的选择性比其他类固醇激素核受体高。 | |||
T14116 |
ACP-105
|
Androgen Receptor | Endocrinology/Hormones |
ACP-105 是选择性的、可口服的雄激素受体调节剂 , 能够作用于野生型 AR (pEC50:9.0)和 T877A 突变型 AR (pEC50:9.3)。 | |||
T3618 |
GSK-2881078
GSK2881078,GSK 2881078 |
Androgen Receptor | Endocrinology/Hormones |
GSK-2881078 是雄激素受体调节器,可用于精神萎顿的研究。 | |||
T2408 |
Ostarine
MK-2866,GTX-024,Enobosarm |
Androgen Receptor | Endocrinology/Hormones |
Ostarine (MK-2866) 是一种具有合成代谢活性的非甾体药物。选择性雄激素受体调节剂 (SARM) GTx-024 旨在像睾酮一样发挥作用,从而促进和/或维持性欲、生育能力、前列腺生长以及肌肉生长和力量。模仿睾酮的作用,这种药物可以增加瘦体重,从而改善癌症恶病质高代谢状态下的肌肉萎缩。 | |||
T20789 |
S-23
(S)-3-(4-chloro-3-fluorophenoxy)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide,S23 |
Androgen Receptor | Endocrinology/Hormones |
S-23 ((S)-3-(4-chloro-3-fluorophenoxy)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide) 是口服选择性雄激素受体调节剂(Ki:1.7 nM)。它能够诱导 CV-1 细胞雄激素受体介导的转录激活,提高去势大鼠前列腺、精囊和肛提肌重量。 | |||
T2108 |
Andarine
S-4,GTx-007 |
Androgen Receptor | Endocrinology/Hormones |
Andarine (GTx-007) 是一种选择性的、具有口服活性的、非甾体受体雄激素受体(AR)调节剂 (SARM) 和部分激动剂,Ki=4 nM。它是一种具有较强活性的、具有组织选择性的 SARM。 | |||
T28650 |
S-40503
|
||
S-40503 is an investigational selective androgen receptor modulator (SARM). | |||
T33944 |
PF-06260414
PF 06260414,PF06260414,PF-6260414,PF 6260414,PF6260414 |
||
PF-06260414 is a selective androgen receptor modulator or SARM used to treat muscle weakness. | |||
T27824 |
LG-121071
LGD 121071,LGD-121071,LGD121071,LG 121071 |
||
LG-121071 is a selective androgen receptor modulator (SARM) with orally active. LG-121071 acts as a high-affinity full agonist of the androgen receptor (AR) (Ki = 17 nM). | |||
T15750 |
Ligandrol
LGD-4033 |
Androgen Receptor | Endocrinology/Hormones |
Ligandrol 是一种新型的非甾体口服 SARM,以高亲和力(Ki:1 nM)和选择性与雄激素受体结合。 | |||
T27676 |
JNJ-37654032
|
||
JNJ-37654032 is a nonsteroidal AR ligand with mixed agonist and antagonist activity. It is an orally active SARM with muscle selectivity. It stimulated growth of the levator ani muscle with ED(50) 0.8 mg/kg, stimulating maximal growth at a dose of 3mg/kg. | |||
T71118 | NEP-28 | ||
NEP-28 is an AR agonist. NEP28 is a new SARM exhibiting high selectivity for androgen receptor. NEP28 showed tissue-selective effect equivalent to or higher than existing SARMs. In addition, the administration of NEP28 increased the activity of neprilysin, a known Aβ-degrading enzyme. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN2055 |
Periplogenin 3-[O-β-glucopyranosyl-(1→4)-β-sarmentopyranoside]
4)-beta-sarmentopyranoside]'>Periplogenin 3-[O-beta-glucopyranosyl-(1->4)-beta-sarmentopyranoside],异杠柳毒苷 |
Others | Others |
Periplogenin 3-[O-beta-glucopyranosyl-(1->4)-beta-sarmentopyranoside] is a natural product from Periploca sepiumBge. | |||
TN4949 |
Sarmentocymarin
|
Others | Others |
Sarmentocymarin is a cardiac glucoside. | |||
T81211 | Sarmenoside III | ||
Sarmenoside III,一种从垂盆草(Sedum sarmentosum)分离得到的黄酮醇苷,具有肝脏保护活性。 | |||
TN6781 |
SarMentine
|
||
SarMentine 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6781,CAS号为 78910-33-5。 | |||
TN2181 | Sarmentosin | Others | Others |
Sarmentosin significantly lowers the SGPT level of patients suffering from chronic viral hepatitis, and shows a suppressive effect on cell-mediated immune responses in mice. It shows a good effect in lowering serum glutamate-pyruvate transaminase. | |||
T81212 |
Sarmenoside II
|
||
Sarmenoside II为一种黄酮醇苷,能够抑制脂质积聚。该化合物在HepG2细胞中抑制油酸白蛋白诱导的脂质积累,其100 μM浓度下的抑制率约为30%。 |