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30

抑制剂 & 化合物

2

天然产物

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Cat. No. Product Name Target Signaling Pathways
T8348 Phentolamine

Adrenergic Receptor GPCR/G Protein; Neuroscience
Phentolamine 是一种 alpha-1 和 alpha-2 选择性肾上腺素能受体拮抗剂。
T8405 Vardenafil hydrochloride

伐地那非,盐酸伐地那非

PDE Metabolism
Vardenafil hydrochloride 是口服具有活性的、高效的、选择性的磷酸二酯酶 5抑制剂。它对 PDE1 (180 nM),PDE6 (11 nM),PDE2,PDE3,PDE4 (>1000 nM) 具有选择性。它能够非竞争性地抑制环磷酸鸟苷水解,提高 cGMP 水平。它可用于勃起功能障碍的研究。
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。
T4097 Vardenafil hydrochloride trihydrate

Vardenafil HCl Trihydrate,BAY38-9456,盐酸瓦地那非三水合物

PDE Metabolism
Vardenafil hydrochloride trihydrate (BAY38-9456) 是一种新型 PDE 抑制剂,对 PDE5 和 PDE1 的 IC50 分别为 0.7 和 180 nM。
T2334 Avanafil

阿伐那非,TA1790

PDE Metabolism
Avanafil (TA1790) 是一种高活性PDE-5抑制剂,IC50=5.2 nM,对PDE1,PDE6和PDE11活性较低。
T1275 Phentolamine mesylate

Phentolamine methanesulfonate,甲磺酸酚妥拉明,Phentolamine mesilate

Adrenergic Receptor GPCR/G Protein; Neuroscience
Phentolamine mesylate (Phentolamine methanesulfonate) 是一种非选择性的、可逆的,具有口服活性的 α1 和 α2 肾上腺素能受体阻滞剂,能够扩张使血管,降低周围血管阻力。它可用于研究嗜铬细胞瘤相关的高血压,心力衰竭和勃起功能障碍。
T16079 Mirodenafil

米罗那非,SK3530

PDE Metabolism
Mirodenafil 是一种磷酸二酯酶5(PDE-5)抑制剂,可用于勃起功能紊乱的研究。
TQ0126 Mirodenafil dihydrochloride

SK-3530 dihydrochloride,米罗那非二盐酸盐

PDE Metabolism
Mirodenafil dihydrochloride 是一种磷酸二酯酶5(PDE-5)抑制剂,可作用于勃起功能紊乱的研究。
T4480 Vardenafil dihydrochloride

Levitra,Vardenafil Hydrochloride,二盐酸伐地那非

PDE Metabolism
Vardenafil dihydrochloride (Levitra) 是一种新型 PDE 抑制剂,对 PDE5 和 PDE1 的 IC50 分别为 0.7 和 180 nM。
T27122 Dasantafil

SCH446132,SCH-446132,SCH 446132

PDE Metabolism
Dasantafil (SCH446132) 是一种小分子磷酸二酯酶-5A(PDE5A)抑制剂,可用于治疗泌尿生殖系统疾病和研究勃起功能障碍。
T7346 Lodenafil

Hydroxyhomosildenafil,羟基豪莫西地那非

PDE Metabolism
Lodenafil (Hydroxyhomosildenafil) 是一种有效的磷酸二酯酶 5 型(PDE5)抑制剂,可用于勃起功能障碍的研究。
T6147 Nortadalafil

Demethyl Tadalafil,去甲基他达那非

PDE Metabolism
Nortadalafil (Demethyl Tadalafil) 是 demethyl Tadalafil,是一种 PDE5 抑制剂。
T0467 Sildenafil citrate

UK-92480 citrate,西地那非柠檬酸盐,枸橼酸西地那非

Apoptosis; PDE; Autophagy Apoptosis; Autophagy; Metabolism
Sildenafil citrate (UK-92480 citrate) 是一种磷酸二酯酶 5 抑制剂,IC50为 5.22 nM。
T9847 TLC2976-0103

ROCK1-IN-1 是一种ROCK1抑制剂,Ki 值为 540 nM。ROCK1-IN-1 可用于高血压、青光眼、勃起功能障碍的研究。
T22019 ABT 724 trihydrochloride

Dopamine Receptor GPCR/G Protein; Neuroscience
ABT 724 trihydrochloride 是一种有效的选择性 D4 受体激动剂(EC50 = 12.4 nM,14.3 nM 和 23.2 nM,分别对人、大鼠和雪貂)。 ABT-724 trihydrochloride 可用于勃起功能障碍研究。
TP1097 Melanotan I

美拉诺坦,美拉诺坦 I,[Nle4,D-Phe7]-α-MSH,Afamelanotide,MT-I

Others Others
Melanotan I 是一种非特异性黑素皮质激素受体 (MCR) 激动剂, 是一种 α- 黑素细胞刺激激素 (α-MSH) 类似物,皮下注射可增加黑色素在皮肤中的含量。Melanotan I 可用于辅助美黑。Melanotan I 可用于预防阳光诱发皮肤癌,可用于研究黑色素瘤和男性勃起功能障碍。
T29048 UK 357903

UK357903,UK-357903

UK 357903, a phosphodiesterase 5A (PDE5A) inhibitor, is used potentially for the treatment of erectile dysfunction.
T29194 Yonkenafil HCl

Yonkenafil hydrochloride

Yonkenafil HCl, a PDE5 inhibitor, is used potentially for the treatment of erectile dysfunction.
T70019 Tadalafil hydroxypiperidone

Tadalafil hydroxypiperidone is an impurity of Tadalafil -- a phosphodiesterase 5-inhibitor used for the treatment of erectile dysfunction.
TP1016 Aviptadil

Vasoactive Intestinal Peptide (human, rat, mouse, rabbit, canine, porcine),阿肽地尔

Aviptadil (INN) is an analog of vasoactive intestinal polypeptide (VIP) for the treatment of erectile dysfunction.
T70629 Acetaminotadalafil

Acetaminotadalafil is a new analogue of Tadalafil used for the treatment of erectile dysfunction. It acts as a phosphodiesterase 5 inhibitor.
T20024 Tadalafil, (6R ,12aS)-

Tadalafil (6R ,12aS)- Lilly,Tadalafil specified impurity A,(-)-Tadalafil (6R ,12aS) diastereomer

Tadalafil is a carboline derivative and Phosphodiesterase 5 Inhibitor. It is used primarily to treat Erectile dysfunction, Benign Prostatic Hyperplasia, and Primary Pulmonary Hypertension.
T79091 Bivamelagon hydrochloride

MC-4R Agonist 2 hydrochloride

Melanocortin Receptor GPCR/G Protein; Neuroscience
MC-4R Agonist 2 hydrochloride (实施例 1) 是用于研究肥胖、糖尿病、炎症和勃起功能障碍的MC4R激动剂。
T37325 Lodenafil carbonate

Lodenafil carbonate, a prodrug dimer that delivers Lodenafil in vivo, is an orally active inhibitor of phosphodiesterase type 5 (PDE5), indicated for the treatment of erectile dysfunction (ED)[1][2].
T73473 TPN729

TPN729 是一种选择性 phosphodiesterasetype 5 (PDE5) 抑制剂,IC50值为 2.28 nM。TPN729 影响勃起功能,可用于勃起功能障碍的研究。
T73354 TPN729MA

TPN729 maleate

TPN729MA (TPN729 maleate) 是一种选择性 phosphodiesterasetype 5 (PDE5) 抑制剂,IC50值为 2.28 nM。TPN729MA 影响勃起功能,可用于勃起功能障碍的研究。
T74372 N-Desalkyludenafil

N-Desalkyludenafil 是 Udenafil 的代谢物。Udenafil 是一种PDE5抑制剂,用于研究勃起功能障碍。
T83536 (R)-Avanafil

(R)-TA1790

(R)-Avanafil ((R)-TA1790),为选择性PDE5抑制剂,IC50值为5.2 nM,主要用于勃起功能障碍研究。
T79090 Bivamelagon

MC-4R Agonist 2

Melanocortin Receptor GPCR/G Protein; Neuroscience
MC-4R Agonist 2 (实施例 1)作为MC4R激动剂,适用于肥胖、糖尿病、炎症及勃起功能障碍的研究领域。
T69127 Moxisylyte

Moxisylyte, also known as thymoxamine, is a drug used in urology for the treatment of erectile dysfunction. It is an α1-adrenergic antagonist. Moxisylyte is also used for the short-term treatment of primary Reynaud's syndrome, a condition where the fingers and toes become discoloured in response to cold or emotional distress. Moxisylyte helps by improving blood circulation to the extremities. It is also used locally in the eye to reverse the mydriasis caused by phenylephrine and other sympathomi...

化合物

Phentolamine
Cat.No: T8348
Synonym:
Target: Adrenergic Receptor
Vardenafil hydrochloride
Cat.No: T8405
Synonym: 伐地那非,盐酸伐地那非
Target: PDE
Vardenafil
Cat.No: T0096
Synonym: 伐地那非,Vivanza,Levitra,Vardenafil hydrochloride
Target: PDE
Vardenafil hydrochloride trihydrate
Cat.No: T4097
Synonym: Vardenafil HCl Trihydrate,BAY38-9456,盐酸瓦地那非三水合物
Target: PDE
Avanafil
Cat.No: T2334
Synonym: 阿伐那非,TA1790
Target: PDE
Phentolamine mesylate
Cat.No: T1275
Synonym: Phentolamine methanesulfonate,甲磺酸酚妥拉明,Phentolamine mesilate
Target: Adrenergic Receptor
Mirodenafil
Cat.No: T16079
Synonym: 米罗那非,SK3530
Target: PDE
Mirodenafil dihydrochloride
Cat.No: TQ0126
Synonym: SK-3530 dihydrochloride,米罗那非二盐酸盐
Target: PDE
Vardenafil dihydrochloride
Cat.No: T4480
Synonym: Levitra,Vardenafil Hydrochloride,二盐酸伐地那非
Target: PDE
Dasantafil
Cat.No: T27122
Synonym: SCH446132,SCH-446132,SCH 446132
Target: PDE
Lodenafil
Cat.No: T7346
Synonym: Hydroxyhomosildenafil,羟基豪莫西地那非
Target: PDE
Nortadalafil
Cat.No: T6147
Synonym: Demethyl Tadalafil,去甲基他达那非
Target: PDE
Sildenafil citrate
Cat.No: T0467
Synonym: UK-92480 citrate,西地那非柠檬酸盐,枸橼酸西地那非
Target: Apoptosis, PDE, Autophagy
TLC2976-0103
Cat.No: T9847
Synonym:
Target:
ABT 724 trihydrochloride
Cat.No: T22019
Synonym:
Target: Dopamine Receptor
Melanotan I
Cat.No: TP1097
Synonym: 美拉诺坦,美拉诺坦 I,[Nle4,D-Phe7]-α-MSH,Afamelanotide,MT-I
Target: Others
UK 357903
Cat.No: T29048
Synonym: UK357903,UK-357903
Target:
Yonkenafil HCl
Cat.No: T29194
Synonym: Yonkenafil hydrochloride
Target:
Tadalafil hydroxypiperidone
Cat.No: T70019
Synonym:
Target:
Aviptadil
Cat.No: TP1016
Synonym: Vasoactive Intestinal Peptide (human, rat, mouse, rabbit, canine, porcine),阿肽地尔
Target:
Acetaminotadalafil
Cat.No: T70629
Synonym:
Target:
Tadalafil, (6R ,12aS)-
Cat.No: T20024
Synonym: Tadalafil (6R ,12aS)- Lilly,Tadalafil specified impurity A,(-)-Tadalafil (6R ,12aS) diastereomer
Target:
Bivamelagon hydrochloride
Cat.No: T79091
Synonym: MC-4R Agonist 2 hydrochloride
Target: Melanocortin Receptor
Lodenafil carbonate
Cat.No: T37325
Synonym:
Target:
TPN729
Cat.No: T73473
Synonym:
Target:
TPN729MA
Cat.No: T73354
Synonym: TPN729 maleate
Target:
N-Desalkyludenafil
Cat.No: T74372
Synonym:
Target:
(R)-Avanafil
Cat.No: T83536
Synonym: (R)-TA1790
Target:
Bivamelagon
Cat.No: T79090
Synonym: MC-4R Agonist 2
Target: Melanocortin Receptor
Moxisylyte
Cat.No: T69127
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T2142 Yohimbine hydrochloride

盐酸育亨宾,Antagonil,Yohimbine HCl

Adrenergic Receptor GPCR/G Protein; Neuroscience
Yohimbine hydrochloride (Antagonil) 是一种植物生物碱,具有 α-2-肾上腺素能阻断活性。它被用作散瞳药和治疗勃起功能障碍。
T1626 Prostaglandin E1

前列地尔,PGE1,列腺素E1,Alprostadil

Endogenous Metabolite; Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation; Metabolism
Prostaglandin E1 (Alprostadil) 是一种前列腺素受体配体,对小鼠 EP1、EP2、EP3、EP4和 IP 的 Ki 值分别为 36、10、1.1、2.1 和 33 nM。它诱导血管舒张并抑制血小板聚集,可作为血管扩张剂用于外周血管疾病的研究。

天然产物

Yohimbine hydrochloride
Cat.No: T2142
Synonym: 盐酸育亨宾,Antagonil,Yohimbine HCl
Target: Adrenergic Receptor
Prostaglandin E1
Cat.No: T1626
Synonym: 前列地尔,PGE1,列腺素E1,Alprostadil
Target: Endogenous Metabolite, Prostaglandin Receptor
TargetMol Loading
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