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Cat. No. | Product Name | Target | Signaling Pathways |
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T4297 |
Flibanserin
BIMT-17BS,氟立班丝氨,Girosa,BIMT-17 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Flibanserin (Girosa) 一种具有口服活性的 5-HT1A 受体激动剂和 5-HT2A 受体拮抗剂,Ki 值分别为 1 和 49 nM。它与多巴胺 D4 受体结合,Ki 值在 4 到 24 nM 之间。它是一种血清素能抗抑郁药,用于治疗性欲减退症。 | |||
T6461 |
Dapoxetine hydrochloride
LY-210448,LY-210448 hydrochloride,Dapoxetine HCl,盐酸达泊西汀,Priligy |
5-HT Receptor; Serotonin Transporter | GPCR/G Protein; Neuroscience |
Dapoxetine hydrochloride (LY-210448 hydrochloride) 是一种具有口服活性的、选择性的血清素再摄取 (serotonin reuptake) 抑制剂 (SSRI),可用于研究早泄 (PE) 。 | |||
T0039 |
Dapoxetine
达波西汀,Dapoxetina,Dapoxetinum |
Others; 5-HT Receptor | GPCR/G Protein; Neuroscience; Others |
Dapoxetine (Dapoxetina) 是一种选择性5-羟色胺再摄取抑制剂,用于治疗早泄。 | |||
T31081L |
CP 866087
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
CP 866087 是一种阿片受体拮抗剂,可用于研究女性性功能障碍。 | |||
T0384 |
Estradiol benzoate
Benzoestrofol,Benzhormovarine,苯甲酸雌二醇,Benovocylin |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Estradiol benzoate (Benzhormovarine) 是一种类固醇性激素,是一种雌二醇的前体药物。它表现出轻微的合成代谢特性,增加血液凝固性。 | |||
T31081 |
CP-866087
CP 866087,UNII-MDH21334PI,CP-866,087,CP866087 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
CP-866087 是一种新型、有效和选择性的μ阿片受体拮抗剂,用于研究女性性功能障碍。 | |||
T10918 |
NEP-IN-1
|
Neprilysin | Metabolism |
NEP-IN-1 是中性肽链内切酶 (NEP) 的抑制剂 (IC50 = 2 nM)。 | |||
T72039 |
CLK1-IN-3
|
DYRK; CDK; Autophagy | Autophagy; Cell Cycle/Checkpoint; Tyrosine Kinase/Adaptors |
CLK1-IN-3 是一种+具有选择性和高效的性 Clk1 抑制剂,其 IC50 为 5 nM,比对 Dyrk1A 的亲和力高300对倍。CLK1-IN-3 对 Clk2 和 Clk4 也显示出高效的抑制作用,IC50 值分别为 42 和 108 nM。CLK1-IN-3 在体外有效诱导自噬 (autophagy),可用于预防和人治疗急性肝损伤 (ALI)。 | |||
T0096 |
Vardenafil
伐地那非,Vivanza,Levitra,Vardenafil hydrochloride |
PDE | Metabolism |
Vardenafil (Vivanza) 是选择性、高效的、具有口服活性的磷酸二酯酶5抑制剂,IC50=0.7 nM。它能够非竞争性地抑制环磷酸鸟苷水解,从而提高 cGMP 水平。它对 PDE1 (180 nM),PDE6 (11 nM),PDE2,PDE3,PDE4 (>1000 nM) 具有选择性。它可用于研究勃起功能障碍。 | |||
T27826 |
LGD-2941
LGD 2941,LGD2941 |
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LGD-2941 is an androgen receptor modulator. LGD-2941 is used for the treatment of hypogonadism, female sexual dysfunction and menopausal syndrome. | |||
T26516 |
ABH Hydrochloride
6-borono-L-norleucine,ABH HCl |
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ABH Hydrochloride is an arginase inhibitor, it enhances both male and female sexual arousal responses. | |||
T29053 |
UK-447841
UK 447841 |
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UK-447841, a neutral endopeptidase (NEP) inhibitor, is used potentially for the treatment of female sexual dysfunction. | |||
T71841 |
MMV085203
|
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MMV08520 is a novel inhibitor of Plasmodium falciparum, killing both blood- and sexual-stage P. falciparum parasites. | |||
T10230 |
MC-4R Agonist 1
|
Others | Others |
MC-4R Agonist 1 is an agonist of human melanocortin-4 receptor (MC-4R) and can be used in the research of sexual dysfunction, obesity, and diabetes. | |||
T24839 |
Stampidine
HI-113,HI 113,HI113 |
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Stampidine can prevent the sexual transmission of HIV-1. It exhibited remarkable subnanomolar to low nanomolar in vitro antiretroviral potency against nucleoside reverse transcriptase inhibitor-resistant primary clinical HIV isolates, non-nucleoside RT-re | |||
T81599 |
Orenetide
|
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Orenetide为旨在HSDD(性欲减退症)治疗中恢复伴随功能的研究用多肽。 | |||
T15749 |
LGD-2226
|
Androgen Receptor | Endocrinology/Hormones |
LGD-2226 is a selective and orally active androgen receptor modulator (EC50: 0.2 nM, Ki: 1.5 nM for the human androgen receptor). LGD-2226 can be used for muscle wasting, osteoporosis, and sexual dysfunction. | |||
T27400 |
Ganaplacide
KAF 156,KAF-156,GNF-156,GNF 156,GNF156,KAF156 |
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Ganaplacide is an antimalarials with activity against asexual and sexual blood stages and the preerythrocytic liver stages of malarial parasites. KAF156 showed antimalarial activity without evident safety concerns in a small number of adults with uncompli | |||
T83544 |
(E)-5-Octadecene
(E)-Octadec-5-ene |
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(E)-Octadec-5-ene ((E)-5-Octadecene),作为一种性信息素或相关化学物质,能够抑制Chilo suppressalis Walker(水稻螟虫蛾)雌蛾的性吸引力。 | |||
T72380 |
PI3K/mTOR Inhibitor-13
|
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PI3K/mTOR Inhibitor-13 是一种具有口服活性的磷酸肌醇 3-激酶 (PI3K) 和mTOR 激酶双重抑制剂。PI3K/mTOR Inhibitor-13 在性疾病、实体瘤和特发性肺纤维化 (IPF) 中有潜在应用。 | |||
T69627 | Dapivirine HCl | ||
Dapivirine HCl is the salt form of Dapivirine, also known as TMC120, a non-nucleoside inhibitor for HIV reverse transcriptase with IC50 of 24 nM. The HIV-1 replication inhibitor dapivirine (DPV) is one of the most promising drug candidates being used in topical microbicide products for prevention of HIV-1 sexual transmission. | |||
T68836 |
ADS-J1
|
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ADS-J1 is an HIV-1 entry inhibitor that potently inhibits seminal amyloid fibrillization and block fibril-mediated enhancement of viral infection. Semen-derived amyloid fibrils, comprising SEVI (semen-derived enhancer of viral infection) fibrils and SEM1 fibrils, may remarkably enhance HIV-1 sexual transmission and are potential targets for the development of an effective microbicide. | |||
T37922 |
7(Z),11(Z)-Pentacosadiene
|
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Unsaturated, long-chain hydrocarbons are found on the cuticles of insects and can act as pheromones. In mature Drosophila melanogaster, certain cuticular hydrocarbons are sexually dimorphic: males synthesize 23- and 25-C monoenes and females produce 27- and 29-C dienes. Each of these lipids plays specific roles in regulating male sexual behavior, with dienes stimulating courtship. 7(Z),11(Z)-Pentacosadiene is a 25-C hydrocarbon that is found in low abundance on cuticles of mature Drosophila fema... | |||
T62324 |
Flibanserin hydrochloride
|
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Flibanserin (BIMT-17; BIMT-17BS) hydrochloride 是一种口服具有活力的 5-羟色胺的 5-HT1A 受体激动剂 (Ki: 1 nM) 和 5-HT2A (Ki: 49 nM) 受体拮抗剂。Flibanserin hydrochloride 同时可以结合多巴胺 D4 受体 (Ki: 4-24 nM)。Flibanserin hydrochloride 具有抗抑郁和抗焦虑的效果,能够用于性欲减退 (HSDD) 的研究。 | |||
T62677 | Ganaplacide hydrochloride | ||
Ganaplacide (KAF156) hydrochloride 是一种首创的、口服具有活力的咪唑哌嗪类抗疟药 (antimalarial)。Ganaplacide hydrochloride 对多种疟原虫(包括耐药寄生虫)有作用。Ganaplacide hydrochloride 对无性和有性血液阶段以及肝脏阶段均具有杀虫效果。 | |||
T69215 | Ambrein | ||
Ambrein is a triterpene alcohol that is the chief constituent of ambergris, a secretion from the digestive system of the sperm whale, and has been suggested as the possible active component producing the supposed aphrodisiac effects of ambergris. It serves as the biological precursor for a number of aromatic derivatives such as ambroxan and is thought to possess fixative properties for other odorants. It has been shown to act as an analgesic and it has been proven to increase sexual behavior in ... | |||
T37924 |
7(Z)-Tricosene
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7(Z)-Tricosene is an unsaturated cuticular hydrocarbon that acts as a pheromone in some insects, including Drosophila. While it is present in both sexes of some Drosophila species, it is abundant in males, but not females, of D. melanogaster and D. sechellia. In these species, 7(Z)-tricosene prevents or reduces male courtship behavior and increases female sexual receptivity. It is absent from virgin D. melanogaster females, but is transferred from males to females during mating. In addition, mat... | |||
T61572 |
FNDR-20123 free base
|
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FNDR-20123 free base 是一种有效、安全、首创的抗疟疾HDAC 抑制剂,对疟原虫和人类 HDAC 的IC50分别为 31 nM 和 3 nM。FNDR-20123 free base 对恶性疟原虫 (Plasmodium falciparum) 无性期 (IC50=41 nM) 和性血期 (雄性配子体 IC50=190 nM) 具有抗疟疾活性。FNDR-20123 free base 抑制 HDAC1,HDAC2,HDAC3,HDAC6,HDAC8 的 IC50分别为 25,29,2,11,282 nM,并在纳摩尔浓度下抑制 III 类 HDAC 亚型。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T3409 |
Plantamajoside
Y0160,C10485,大车前苷,车前子甙 |
Others | Others |
Plantamajoside (Y0160) 是一种苯丙烷类糖苷,从车前Plantago asiaticaL.中分离出来得到。它对 LPS 诱导的急性肺损伤小鼠模型具有保护作用。它对肺部炎症具有潜在的研究价值。 | |||
T2A2532 |
L-Histidine
Glyoxaline-5-alanine,L-(-)-Histidine,L-组氨酸,histidine,组氨酸,L-Hisidine |
Mitochondrial Metabolism; Endogenous Metabolite | Metabolism |
L-Histidine (L-(-)-Histidine) 是人类生长和组织修复所需的一种半必需氨基酸(儿童应从食物中获得)。 L-Histidine 是线粒体谷氨酰胺转运的抑制剂。 | |||
T1048 |
Estradiol
雌二醇,E2,17β-Estradiol,17β-Oestradiol,β-Estradiol |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Estradiol (E2) 是一种天然的类固醇性激素,对于女性生育能力和第二性征的维持至关重要。Estradiol 通过雌激素受体 β (ERβ) 上调 IL-6 表达。 |