237
33
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19717 |
Cyclo-L-Trp-L-Trp
|
Antifungal | Microbiology/Virology |
Cyclo-L-Trp-L-Trp 是一种广谱抗真菌剂。它还诱导组蛋白的高度乙酰化。 | |||
T15457L |
H-Lys-Trp-Lys-OH acetate
H-Lys-Trp-Lys-OH acetate(38579-27-0 free base) |
Antiviral; Antibacterial | Immunology/Inflammation; Microbiology/Virology |
H-Lys-Trp-Lys-OH acetate 是一种具有抗菌和抗病毒活性的肽。 | |||
TP1426 |
His-[D-2-ME-Trp]-Ala
|
Others | Others |
His-[D-2-ME-Trp]-Ala 是生长激素海沙瑞林的一个片段。 | |||
TP2305 |
pGlu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val
|
Others | Others |
pGlu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val 是一种肽。 | |||
T24903 |
TRP-601
TRP601 |
||
TRP-601 is a caspase inhibitor. | |||
T20540 |
N-Valyltryptophan
二肽-2,Val-trp,L-Valyl-L-tryptophan |
Others | Others |
N-Valyltryptophan (Val-trp) 是蛋白质分解代谢或蛋白质消化的不完全分解产物。 | |||
T8318 |
BNC210
H-Ile-Trp-OH,IW-2143 |
AChR | Neuroscience |
BNC210 (IW-2143) 是一种α7 nAChR 负变构调节剂,在焦虑和抑郁动物模型中有活性。 | |||
T76626 |
H-Trp-Trp-Trp-OH
|
||
H-Trp-Trp-Trp-OH 是一种三肽,由色氨酸组成。H-Trp-Trp-Trp-OH 具有抗菌活性。 | |||
TP1251L |
N-terminally acetylated Endomorphin-1 acetate
Ac-L-Tyr-L-Pro-L-Trp-L-Phe-CONH2 |
Others | Others |
N-terminally acetylated Endomorphin-1 acetate (Ac-L-Tyr-L-Pro-L-Trp-L-Phe-CONH2) 是一种修饰的 Endomorphin-1。 | |||
T39111 | Fmoc-D-Trp(Boc)-OH | ||
Fmoc-D-Trp(Boc)-OH is a labile ADC linker employed for synthesizing antibody-drug conjugates (ADCs). | |||
T19326 | Fmoc-Trp(Me)-OH | Others | Others |
Fmoc-Trp(Me)-OH is synthesized by 1-Methyl-Ltrypthophan and N-(9-Fluorenylmethoxycarbonyloxy)succinimide (Fmoc-ONSu) and can be used for peptide or protein synthesis. | |||
T15457 |
H-Lys-Trp-Lys-OH
|
Others | Others |
H-Lys-Trp-Lys-OH is a small molecule peptide that shows antibacterial and antiviral activities. | |||
T33079 | Lys-psi(CH2NH)-trp(nps)-ome | ||
Lys-psi(CH2NH)-trp(nps)-ome peptide bond replaced by CH2NH group. | |||
T41049 |
Fmoc-Trp(Boc)-Ser(psi(Me,Me)pro)-OH
|
||
Fmoc-Trp(Boc)-Ser(psi(Me,Me)pro)-OH is a dipeptide. | |||
TP1893L1 |
[D-Trp8]-γ-MSH acetate(321351-81-9 free base)
|
Melanocortin Receptor | GPCR/G Protein; Neuroscience |
[D-Trp8]-γ-MSH acetate(321351-81-9 free base) 是选择性黑皮质素 3 (MC3) 受体激动剂(对人 MC3、MC5 和 MC4 受体的 IC50 值分别为 6.7、340 和 600 nM)。显示有抗炎功效。 | |||
T83748 |
RW4 TFA
(RW)4-NH2,Arg-Trp-Arg-Trp-Arg-Trp-Arg-Trp-NH2 |
||
RW4为一种抗菌肽,对E. coli和S. aureus具有活性(IC50s分别为9.6和5.1 µM)。RW4同时能诱导分离的绵羊红细胞的溶血作用。 | |||
T76575 |
Arg-Trp
|
||
Arg-Trp 是由精氨酸和色氨酸组成的二肽,Arg-Trp 辛酯的类似物显示出抗菌活性。 | |||
T39311 |
Tyrosinase-related Protein 2 (TRP-2) (181-188)
|
||
Tyrosinase-related Protein 2 (TRP-2) (181-188) is a peptide derived from the tyrosinase-related protein 2 (TRP-2), specifically corresponding to residues 180-188. It is the primary epitope within TRP-2 that is recognized by anti-B16 CTLs. Moreover, It is a peptide that conforms to the binding motif of the MHC class I H2-Kb. | |||
T41080 |
Fmoc-Trp(Boc)-Thr(psi(Me,Me)pro)-OH
|
||
Fmoc-Trp(Boc)-Thr(psi(Me,Me)pro)-OH is a dipeptide. | |||
T7769 |
Nonapeptide-1
Met-Pro-D-Phe-Arg-D-Trp-Phe-Lys-Pro-Val-,九胜肽-1,Melanostatine™ 5 |
Others | Others |
Nonapeptide-1 (Melanostatine™ 5) 可以抑制黑色素的合成,这使得它对治疗某些皮肤病很感兴趣。 | |||
T83747 |
RW3 TFA
(RW)3-NH2,Arg-Trp-Arg-Trp-Arg-Trp-NH2 |
||
RW3是一种抗微生物肽,对大肠杆菌(E. coli)和金黄色葡萄球菌(S. aureus)具有活性,其半抑制浓度(IC50s)分别为16 µM和8 µM。RW3还能诱导分离的绵羊红细胞溶解。 | |||
TP2460 |
Lys-phe-phe-phe-ile-ile-trp-och3
|
||
Lys-phe-phe-phe-ile-ile-trp-och3 is a hydrophobic peptide which reacts with lipid vesicles. | |||
T64883 |
Z-Trp-OH
|
||
T24447 |
Men 10208
Men-10208,Thr-asp-tyr-trp-val-trp-trp-arg-NH2,Men10208 |
||
Men 10208 is an antagonist of the neurokinin A receptor. | |||
T26334 |
WWamide-1
H-Trp-lys-glu-met-ser-val-trp-NH2 |
||
WWamide-1 is a neuromodulatory peptide isolated from the ganglia of Afrian giant snail, Achatina fulica. | |||
T83746 |
RW2 TFA
(RW)2-NH2,Arg-Trp-Arg-Trp-NH2 |
||
RW2是一种抗微生物肽,对E. coli和S. aureus均有活性(IC50s分别为730和210 µM)。同时,RW2还能诱导分离的绵羊红细胞发生溶血。 | |||
T20481 |
Antagonist G
Arg-trp-N-methyl-phe-trp-leu-met-NH2 |
||
Antagonist G is an anticancer peptide and is also a broad spectrum neuropeptide growth factor antagonist. | |||
T34962 |
Tryptophyl-leucyl-glutamic acid
Trp-leu-glu |
||
Tryptophyl-leucyl-glutamic acid is a tryptophan used for fluorescence spectroscopy. | |||
T25490 |
Hemorphin 4
Tyr-pro-trp-thr |
||
Hemorphin 4 is an endogenous opioid peptide of the hemorphin family which has antinociceptive properties and is derived from the β-chain of hemoglobin in the bloodstream. | |||
T76592 |
H-Lys-Trp-OH
|
||
H-Lys-Trp-OH (KW) 是一种 ACE 抑制肽,IC50为 7.8 μM。 | |||
T29466 |
5-Oxoprolyltryptophan
5-O-Pro-trp |
||
5-Oxoprolyltryptophan is a bioactive chemical. | |||
T64881 |
Z-D-Trp-OH
|
||
T26336 |
WWamide-3
H-Trp-lys-gln-met-ser-val-trp-NH2 |
||
WWamide-3 is a neuromodulatory peptide isolated from the ganglia of African giant snail, Achatina fulica. | |||
T26335 |
WWamide-2
H-Trp-arg-glu-met-ser-val-trp-NH2 |
||
WWamide-2 is used as a neuromodulatory peptide isolated from the ganglia of African giant snail, Achatina fulica. | |||
T82845 |
Boc-D-Trp(For)-OH
|
||
Boc-D-Trp(For)-OH 是一种含有色氨酸的化合物,其生产过程涉及以 Boc 保护的 D-丙氨酸进行氨解反应,随后通过与茚三酮环化反应合成为二肽。该化合物展现出多种药理学效应,能够抑制生长激素的释放,并具有诱导睡眠及抗炎的功效。 | |||
T31915 |
Gatratet
Carbobenzoxy-trp-met-asp-phe-amide |
||
Gatratet is a tetrapeptide. | |||
TP1261 |
Alexamorelin Met 1
(D-Mrp)-Ala-Trp-(D-Phe) |
||
Alexamorelin Met 1 is one of the metabolites of alexamorelin. The heptapeptide Ala-His-D-2-methyl-Trp-Ala-Trp-D-Phe-Lys-NH2 (Alexamorelin) is a synthetic molecule which inhibits growth hormone secretagogue binding in vitro. | |||
T33323 |
Methionyltryptophan
Met-trp,Methionyl-tryptophan,Methionyl tryptophan |
||
Methionyl-Tryptophan is a dipeptide composed of methionine and tryptophan. It is an incomplete breakdown product of protein digestion or protein catabolism. | |||
T30084 |
Antho-rwamide I
Glu-ser-leu-arg-trp-NH2 |
||
Antho-rwamide I is an anthozoan neuropeptide. | |||
T32057 |
Hemorphin 5
Tyr-pro-trp-thr-gln |
||
Hemorphin 5 is an opioid peptide obtained from bovine hemoglobin. | |||
T34819 |
Tetragastrin HCl
Trp-Met-Asp-Phe hydrochloride,Tetragastrin hydrochloride |
||
Tetragastrin HCl is the HCl salt of Tetragastrin, the C-terminal tetrapeptide of gastrin. It has the same physiological and pharmacological activity as gastrin. | |||
T76600 |
Ac-Trp-Glu-His-Asp-Aldehyde
|
||
Ac-Trp-Glu-His-Asp-Aldehyde 是一种有效的选择性 caspase-1抑制剂,Ki 值为 56 pM。 | |||
T40850 |
[D-Trp11]-Neurotensin
[D-Trp11]-Neurotensin |
||
[D-Trp11]-Neurotensin is a compound that functions as a selective antagonist of Neurotensin (NT) in perfused rat hearts, while exhibiting full agonist properties in guinea pig atria and rat stomach strips. Additionally, this compound can inhibit hypotension induced by NT. | |||
T76606 |
Ac-Trp-Glu-His-Asp-AMC
|
||
Ac-Trp-Glu-His-Asp-AMC (AC-WEHD-AMC) 是caspase-1的有效荧光底物。 | |||
T37420 |
Ac-ANW-AMC
Ac-ANW-AMC,Ac-Ala-Asn-Trp-AMC |
||
Ac-ANW-AMC is a fluorogenic substrate for the β5i/LMP7 subunit of the 20S immunoproteasome. [1] Upon cleavage, 7-amino-4-methylcoumarin (AMC) is released and its fluorescence can be used to quantify the activity of the β5i/LMP7 subunit of the 20S immunoproteasome. AMC displays excitation/emission maxima of 340-360/440-460 nm, respectively. Reference[1]. Winter, M.B., La Greca, F., Arastu-Kapur, S., et al. Immunoproteasome functions explained by divergence in cleavage specificity and regulation. ... | |||
T2298 |
ML204
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
ML204 是有效的TRPC4/TRPC5通道选择性抑制剂,相比于 TRPC6 ,对TRPC4/TRPC5通道的选择性高出 19 倍,不影响其他的 TRP 通道和电压门控的钠、钾或 Ca2+通道。 | |||
T40042 |
Evifacotrep
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
Evfacotrep 是一种有效的短期瞬态受体电位通道5 拮抗剂。Evfacotrep 可用于神经系统疾病的研究。 | |||
T33516 |
Msh (5-10), cyclic
Cyclic H-asp-his-phe-arg-trp-lys-NH2 |
||
Msh (5-10), cyclic, as a synthetic peptide, can conjugate with fatty acids for enhanced potency. | |||
T32840 |
Locustakinin
Ala-phe-ser-ser-trp-gly-NH2,Lomk peptide,Locustakinn |
||
Locustakinin is a myotropic peptide. | |||
TP2477 |
VV-Hemorphin-7
Val-val-tyr-pro-trp-thr-gln-arg-phe |
||
VV-Hemorphin-7 is a morphinomimetic peptide. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4833 |
Ac-DL-Trp-OH
N-乙酰-DL-色氨酸,N-Acetyl-DL-tryptophan |
Others; Endogenous Metabolite | Metabolism; Others |
Ac-DL-Trp-OH (N-Acetyl-DL-tryptophan) 是内源性代谢产物的一种。 | |||
T4806 |
H-D-Trp-OH
D-Tryptophan,D-色氨酸 |
Others; Endogenous Metabolite | Metabolism; Others |
H-D-Trp-OH (D-Tryptophan) 是一种色氨酸的 D 型异构体。它偶尔也会在自然界多肽中被发现,如海洋毒肽。 | |||
T4866 |
H-Trp-NH2.HCl
L-Tryptophanamide hydrochloride,L-色氨酰胺盐酸盐,(2S)-2-amino-3-(1H-indol-3-yl)propanamide hydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
H-Trp-NH2.HCl ((2S)-2-amino-3-(1H-indol-3-yl)propanamide hydrochloride) 是一种内源性代谢产物,已在多种生物体液中检测到,如尿液和血液。 | |||
T3208 |
Brevianamide F
Cyclo-L-tryptophyl-L-proline,cyclo-(L-Trp-L-Pro),Cyclo(L-Pro-L-Trp) |
BCRP; PI3K; Antibacterial | Membrane transporter/Ion channel; Microbiology/Virology; PI3K/Akt/mTOR signaling |
Brevianamide F (Cyclo(L-Pro-L-Trp)) 是一种从Colletotrichum gloeosporioides 中分离得到的真菌毒素,属于天然存在的 2,5-二酮哌嗪类,具有抗菌活性。它具有PI3Kα抑制活性,IC50值为 4.8 µM。 | |||
TN6683 | Cyclo(Pro-Trp) | ||
Cyclo(Pro-Trp) and cyclo(Phe-Pro) show broad spectrum antibacterial properties. | |||
T7203 |
Oglufanide
奥谷法奈,L-Glutamyl-L-tryptophan,H-Glu-Trp-OH |
VEGFR; HCV Protease; Endogenous Metabolite | Angiogenesis; Metabolism; Microbiology/Virology; Proteases/Proteasome; Tyrosine Kinase/Adaptors |
Oglufanide (H-Glu-Trp-OH) 是一种从小牛胸腺中分离出来的二肽免疫调节剂,可抑制血管内皮生长因子,可刺激细胞内细菌感染和对丙型肝炎病毒的免疫反应。 | |||
T65245 |
H-Phe-Trp-OH
|
||
H-Phe-Trp-OH 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 T65245,CAS号为 24587-41-5。 | |||
T7177 |
Capsazepine
|
Apoptosis; TRP/TRPV Channel | Apoptosis; Membrane transporter/Ion channel |
Capsazepine 是一种 TRPV1 受体的拮抗剂, IC50值为 562 nM。 它可阻断由激活 TRPV1 离子通道的辣椒素引起的热痛感,是辣椒素拮抗剂。 | |||
T12514 |
Podocarpic acid
|
Others; TRP/TRPV Channel | Membrane transporter/Ion channel; Others |
Podocarpic acid 是一种天然产物,是一种新型 TRPA1 激活剂。 | |||
T2807 |
Caffeic Acid
|
Lipoxygenase; Endogenous Metabolite; TRP/TRPV Channel | Membrane transporter/Ion channel; Metabolism |
Caffeic acid 是5-脂氧合酶和 TRPV1离子通道的双重抑制剂。 | |||
T6S1684 |
8-Gingerol
|
Antioxidant; Antibacterial; TRP/TRPV Channel | Membrane transporter/Ion channel; Microbiology/Virology; oxidation-reduction |
8-Gingerol 分离自姜的根状茎,是口服有效的 TRPV1激活剂,EC50值为5.0 µM。8-Gingerol 抑制 COX-2,还能抑制体外 H. pylori 的生长。 | |||
TN4417 |
Larixyl acetate
|
Others | Others |
Larixyl acetate 是一种生物活性化学物质。 | |||
TQ0001 |
1,4-Cineole
Isocineole,1,4-桉叶素 |
Endogenous Metabolite; TRP/TRPV Channel | Membrane transporter/Ion channel; Metabolism |
1,4-Cineole (Isocineole) 是天然广泛分布的含氧单萜烯,存在于桉树油中,可激活人TRPM8和TRPA1。 | |||
T3727 |
Methyl syringate
Syringic Acid Methyl Ester,丁香酸甲酯 |
TRP/TRPV Channel | Membrane transporter/Ion channel |
Methyl syringate (Syringic Acid Methyl Ester) 是水仙花蜜的化学标记物,是有效的细菌和真菌漆酶酚介质。它也是TRPA1激动剂。 | |||
TCS0102 |
Pulegone
胡薄荷酮,(+)-Pulegone,蒲勒酮,胡薄荷酮,长叶薄荷酮 |
Calcium Channel; Endogenous Metabolite; TRP/TRPV Channel | Membrane transporter/Ion channel; Metabolism |
Pulegone ((+)-Pulegone) 是 Calamintha nepeta (L.) Savi 的精油的主要化学成分,也是禽类驱虫剂之一。它在禽类物种中驱避作用的分子靶点是伤害感受性 TRP 锚蛋 1。它刺激鸡感觉神经元中的 TRPM8 和 TRPA1 通道,并在高浓度下抑制前者但不抑制后者。 | |||
T2952 |
Camphor
樟脑,(±)-Camphor,Bornan-2-one,2-Camphanone,2-Bornanone,Formosa |
Influenza Virus; TRP/TRPV Channel | Membrane transporter/Ion channel; Microbiology/Virology |
Camphor (2-Camphanone) 是一种双环单萜酮,广泛存在于植物中,尤其是樟脑。 它是一种激动剂,局部用作皮肤止痒剂和抗感染剂,具有抗病毒,镇咳和抗癌活性。 | |||
T1407 |
(-)-Menthol
L-Menthol,Levomenthol,(-)-薄荷醇,薄荷冰,Menthomenthol,Menthacamphor |
Opioid Receptor; Endogenous Metabolite; TRP/TRPV Channel | Endocrinology/Hormones; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
(-)-Menthol (Levomenthol) 分离自薄荷油,L-Menthol 是瞬时受体电位 M8 (TRPM8)的激活剂,TRPM8 是 Ca2+-可渗透的非选择性阳离子通道,并增加 [Ca2+]i。L-Menthol 具有抗肿瘤活性。 | |||
TN1377 |
α-Spinasterol
Α-波菜甾醇,alpha-Spinasterol,菠甾醇 |
COX; Antibacterial; TRP/TRPV Channel | Immunology/Inflammation; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
α-Spinasterol 是一种从Spinacia oleracea 分离的瞬时受体电位香草酸 1 拮抗剂,具有抗菌、抗炎、抗抑郁、抗氧化和抗伤害作用。它抑制COX-1和COX-2活性,IC50值分别为 16.17 μM 和 7.76 μM。 | |||
T8307 |
Hydroxy-α-sanshool
羟基-α-山椒素,Hydroxy-α-sanshool |
Endogenous Metabolite; TRP/TRPV Channel | Membrane transporter/Ion channel; Metabolism |
Hydroxy-α-sanshool 是分离自胡椒的烷基酰胺,作为 TRPA1的共价激动剂和 TRPV1的非共价激动剂,EC50分别为69和 1.1 µM。 | |||
T2845 |
Imperatorin
Ammidin,8-Isoamylenoxypsoralen,欧前胡素,8-Isopentenyloxypsoralene,Marmelosin,Pentosalen |
TRP/TRPV Channel; AChR; AChE; NOD | Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience; NF-κB |
Imperatorin (8-Isopentenyloxypsoralene) 是NO synthesis 和BChE 的抑制剂,IC50分别为 9.2 μmol 和 31.4 μmol。它也是TRPV1的微弱激动剂,EC50为 12.6±3.2 μM。 | |||
TN1465 |
Cannabigerol
|
NOS; 5-HT Receptor; ROS | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Cannabigerol 是一种植物大麻素,是一种高亲和力 α2-肾上腺素能受体激动剂、中度亲和力 5-HT1A 受体拮抗剂和低亲和力 CB1/CB2受体拮抗剂。它可降低眼压,有潜力治疗青光眼。 | |||
T3865 |
beta-Eudesmol
β-桉叶醇,Beta-Selinenol,beta-桉叶醇 |
TRP/TRPV Channel; AChR | Membrane transporter/Ion channel; Neuroscience |
beta-Eudesmol (Beta-Selinenol) 是天然的含氧倍半萜烯,可激活hTRPA1,EC50值为 32.5 μM。Beta-Eudesmol 有增加食欲的功效。 | |||
T23107 |
Ononetin
芒柄花酚,2',4'-Dihydroxy-2-(4-methoxyphenyl)acetophenone |
TRP/TRPV Channel | Membrane transporter/Ion channel |
Ononetin (2',4'-Dihydroxy-2-(4-methoxyphenyl)acetophenone) 是天然脱氧安息香素,是有效的TRPM3 通道选择性阻断剂,IC50为 0.3 μM。 | |||
T1321 |
Nonivamide
Nonanoic acid vanillylamide,Pelargonic acid vanillylamide,辣椒素,Vanillyl-N-nonylamide,Pseudocapsaicin |
TRP/TRPV Channel | Membrane transporter/Ion channel |
Nonivamide (Nonanoic acid vanillylamide) 具有激动活性,在静态毒性检测中,4d-EC50为 5.1 mg/L。 | |||
T2994 |
(E)-Cardamonin
Alpinetin chalcone,Cardamomin,小豆蔻明,Cardamonin,(E)-Cardamoni,豆蔻明 |
Apoptosis; TRP/TRPV Channel | Apoptosis; Membrane transporter/Ion channel |
(E)-Cardamonin (Alpinetin chalcone) 是一种新型hTRPA1阳离子通道拮抗剂,IC50值为454 nM。 | |||
T0851 |
Pregnenolone
3β-Hydroxy-5-pregnen-20-one,Arthenolone,孕烯醇酮 |
Cannabinoid Receptor; Endogenous Metabolite; TRP/TRPV Channel; AChR; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Pregnenolone (Arthenolone) 是一种由胆固醇合成的内源性类固醇激素,用于治疗阿尔茨海默病。它是大麻素 CB1受体的信号传导特异性抑制剂,抑制由 CB1受体介导的四氢大麻酚 的作用。它也是 TRPM3通道激活剂,也可弱激活 TRPM1通道。 | |||
T2163 |
Dihydrocapsaicin
CCRIS1589,二氢辣椒素,6,7-Dihydrocapsaicin,8-Methyl-N-vanillylnonanamide |
Others; TRP/TRPV Channel | Membrane transporter/Ion channel; Others |
Dihydrocapsaicin (CCRIS1589) 是一种天然来源的辣椒素,是TRPV1的选择性激动剂,同时可以增加 p-Akt 水平。它可以增强低温诱导的神经保护。 | |||
T14046 |
Anandamide
花生四烯酸乙醇胺,(5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide |
Cannabinoid Receptor; Endogenous Metabolite | GPCR/G Protein; Metabolism |
Anandamide ((5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide) 是一种免疫调节剂,通过大麻素受体 CB1 和 CB2 起作用,还通过中枢神经系统中的其他靶点起作用,如 GPR18/GPR55。 | |||
TN1839 |
Kumatakenin
Jaranol,华良姜素,熊竹素,Kaempferol 3,7-O-dimethyl ether |
Apoptosis; Anti-infection | Apoptosis; Microbiology/Virology |
Kumatakenin 是一种从丁香中分离得到的黄酮类天然产物,可诱导卵巢癌细胞凋亡。 | |||
T2S0799 | Noroxyhydrastinine | Tyrosinase | Proteases/Proteasome |
Noroxyhydrastinine exhibits potent melanogenesis-inhibitory activities, it inhibits melanogenesis, at least in part, by inhibiting the expression of protein levels of tyrosinase, TRP-1, and TRP-2 in α-MSH-stimulated B16 melanoma cells. | |||
TMA0003 | Trans-caffeic acid | cAMP; Tyrosinase | GPCR/G Protein; Proteases/Proteasome |
Trans-caffeic acid stearyl ester is posited to inhibit melanogenesis signaling while suppressing cAMP levels and, subsequently, MC1R, MITF, tyrosinase, TRP-2 and TRP-1 down-regulation, resulting in the suppression of tyrosinase activity, DOPA oxidase activity and melanin synthesis. | |||
TN4179 | Haginin A | ERK; Tyrosinase; Akt | Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Haginin A is an effective inhibitor of hyperpigmentation caused by UV irradiation or by pigmented skin disorders through downregulation via ERK and Akt/PKB activation, MITF, and also by the subsequent downregulation of tyrosinase and TRP-1 production. Hag | |||
T40368 | 4-Ethylresorcinol | ||
4-Ethylresorcinol, a derivative of resorcinol, functions as a tyrosinase substrate, possesses hypopigmentary effects, attenuates mRNA and protein expression of tyrosinase-related protein-2 (TRP-2), and exhibits antioxidative properties through inhibition of lipid peroxidation. |