Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T25107 |
Arginylphenylalaninamide
Rfamide,Arg-phe-NH2 |
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Arginylphenylalaninamide, an FMRamide fragment, may be utilized as a neurotransmitter or neuromodulator by optic lobe neurons of different types. | |||
TP2479 |
Sdrnflrfamide
Ser-asp-arg-asn-phe-leu-arg-phe-NH2 |
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Sdrnflrfamide exhibits FMRFamide-like immunoreactivity isolated from the nervous system of the lobster Homarus americanus. | |||
T31568 |
DP 432
DP432,beta-Alanyl-Arg-Gly-Phe-Phe-Tyr-NH2,DP-432 |
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DP 432 is an insulin hexapeptide fragment. | |||
TP2338 |
Cenupatide
UPARANT,Cenupatide trifluoroacetic acid salt,Ac-Arg-Aib-Arg-α(Me)Phe-NH2) |
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Cenupatide is a urokinase plasminogen activator receptor (uPAR) inhibitor. Cenupatide inhibits uPAR binding to the formyl peptide receptors (FPRs) can improve kidney lesions in a rat model of STZ-induced diabetes. Cenupatide reverted STZ-induced up-regula | |||
T83709 |
LIH383 TFA
Phe-Gly-Gly-Phe-Met-Arg-Arg-Lys-NH2 |
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LIH383是一种趋化因子(C-X-C motif) 受体7 (CXCR7)的多肽激动剂,属于趋化因子和阿片肽清除受体。它专一性激活CXCR7 (EC50 = 0.61 nM),在3 µM浓度时,相比μ-、δ-、κ-阿片受体以及诺氨酸阿片肽(NOP)受体的β-arrestin招募实验中表现出高选择性。LIH383(3 µM)通过阻止U87-ACKR3细胞中,由非选择性阿片受体激动剂dynorphin A诱导的CXCR7对阿片肽的摄取,发挥作用。 | |||
T31808 |
Flrlamide, manduca
Glu-asp-val-val-his-ser-phe-leu-arg-phe-Nh2,Pedvvhsflrf-NH2,Masflrfamide I |
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Flrlamide, manduca is a bioactive peptide extracted from the central nervous system of Manduca sexta. | |||
T25683 |
Leucomyosuppressin
p-Glu-asp-val-asp-his-val-phe-leu-arg-phe-NH2 |
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Leucomyosuppressin, isolated from head extracts of the cockroach Leucophaea maderae, inhibits evoked transmitter release at the mealworm neuromuscular junction. | |||
TP2472 |
Leucopyrokinin
Pglu-thr-ser-phe-thr-pro-arg-leu-NH2 |
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Leucopyrokinin is a myotropic neuropeptide. | |||
T20481 |
Antagonist G
Arg-trp-N-methyl-phe-trp-leu-met-NH2 |
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Antagonist G is an anticancer peptide and is also a broad spectrum neuropeptide growth factor antagonist. | |||
T25092 |
Antho-rpamide II
Glu-asn-phe-his-leu-arg-pro-NH2 |
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Antho-rpamide II is a biologically active neuropeptide isolated from the sea anemone Anthopleura elegantissima. | |||
TP2476 |
Tnrnflrfamide
Thr-asn-arg-asn-phe-leu-arg-phe-NH2,Peptide F(1), lobster,F1 Peptide, lobster,Lobster peptide F1 |
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Tnrnflrfamide is a SCP (small cardioactive peptide)-like peptide found in lobster neurons; exhibits FMRFamide-like immunoreactivity. | |||
T32192 |
IRI-426
Ac-Arg-Pro-Asp-Val-Phe-NH2,IRI426 |
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IRI-426 is a bioactive chemical. | |||
TP2455 |
Locustapyrokinin II
Pglu-ser-val-pro-thr-phe-thr-pro-arg-leu-NH2 |
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Locustapyrokinin II is a member of the FXPRL-amide peptide family isolated from Locusta migratoria. | |||
T33516 |
Msh (5-10), cyclic
Cyclic H-asp-his-phe-arg-trp-lys-NH2 |
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Msh (5-10), cyclic, as a synthetic peptide, can conjugate with fatty acids for enhanced potency. | |||
T32400 |
KKI 8
N-Adamantaneacetyl-phe-arg-ser-val-gln-NH2,KKI8,KKI-8 |
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KKI 8 is a peptide analog. | |||
T25194 |
BW 443C
BW443C,BW-443C,Tyr-arg-gly-(4-nitro-phe)-pro-NH2 |
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BW 443C is a selective agonist of mu-opioid receptor. | |||
T32399 |
KKI 7
KKI-7,N-Cyclohexylacetyl-phe-arg-ser-val-gln-NH2,KKI7 |
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KKI 7 is a peptide analog. | |||
T24901 |
Troponin I (104-115)
Ac-Gly-lys-phe-lys-arg-pro-pro-leu-arg-arg-val-arg-NH2,Tni peptide (104-115) |
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Troponin I is a cardiac and skeletal muscle protein useful in the laboratory diagnosis of a heart attack. Troponin I is a part of the troponin protein complex, where it binds to actin in thin myofilaments to hold the actin-tropomyosin complex in place. | |||
T25507 |
HP 228
HP-228,Ac-Nle-gln-his-D-phe-arg-D-trp-gly-NH2,HP228 |
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HP 228 is a heptapeptide by inhibits the induction of nitric oxide synthase. | |||
T25913 |
P-113
P 113,Ala-lys-arg-his-his-gly-tyr-lys-arg-lys-phe-his-NH2 |
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P-113 is a peptide with antimicrobial activity. | |||
T83666 |
Kisspeptin-10 (zebrafish) TFA
Tyr-Asn-Leu-Asn-Ser-Phe-Gly-Leu-Arg-Tyr-NH2,Kp-10 |
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Kisspeptin-10是一种在斑马鱼的大脑、卵巢和睾丸中表达的神经肽,参与性腺发育和类固醇表达。在10 ng/ml的浓度下使用时,能提高孤立的斑马鱼卵巢滤泡中编码黄体生成素(luteinizing hormone, Lh)受体,以及孕酮受体a (Progestin receptor a, Pra)和Prb的mRNA水平。在0.1和1 µg/g的剂量下给予时,Kisspeptin-10能在雌性金鱼中增加黄体生成素的血清水平,但在雄性金鱼中则不会。 | |||
TP2480 |
Locustamyotropin
Lom-MT,Locustamyotropin I,Lom MT,LomMT,Gly-ala-val-pro-ala-ala-gln-phe-ser-pro-arg-leu-NH2 |
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Locustamyotropin is a novel peptide isolated from Leucophae maderae; stimulates the spontaneous contractions of the hindgut of Leucophaea maderae. | |||
T70836 |
DMJ-I-228
|
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DMJ-I-228 is a specific inhibitor of HIV-1 entry through interaction with the Env spike by virtue of the incorporation of a guandinium group. | |||
T80121 |
Ac-(d-Arg)-CEH-(d-Phe)-RWC-NH2
|
Melanocortin Receptor | GPCR/G Protein; Neuroscience |
Ac-DArg-c[Cys-Glu-His-DPhe-Arg-Trp-Cys]-NH2 是一种环状八肽,能够激活MC4R。该化合物能显著提高心率与血压。 | |||
T80112 |
Arg-Val-(Nle-p-nitro)-Phe-Glu-Ala-Nle-NH2
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Arg-Val-(Nle-p-nitro)-Phe-Glu-Ala-Nle-NH2 是一种用于检测HIV-1蛋白酶活性的荧光底物。 | |||
TP1095 |
Elamipretide
MTP-131,RX-31,SS-31 |
Others | Others |
Elamipretide (MTP-131) 是一种线粒体靶向抗氧化四肽 (D-Arg-dimethylTyr-Lys-Phe-NH2),可以减少有毒活性氧的产生并稳定心磷脂,具有血脑屏障渗透性。Elamipretide 是罕见病巴氏综合征的潜在治疗剂。 | |||
T76449 |
Substance P (alligator)
|
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Substance P (alligator),一种从鳄鱼中提取的神经肽,其氨基酸序列为Arg-Pro-Arg-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2。 | |||
TP1095L |
Elamipretide acetate
MTP 131 acetate,Elamipretide acetate (736992-21-5 Free base) |
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Elamipretide acetate (MTP 131 acetate) 是Elamipretide 衍生物。Elamipretide 是一种小的线粒体靶向四肽(D-Arg-dimethylTyr-Lys-Phe-NH2),可用于研究减少有毒活性氧的产生和稳定心磷脂。 | |||
T81176 |
Ser-parafluoroPhe-Aad-Leu-Arg-Asn-Pro-NH2
|
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Ser-parafluoroPhe-Aad-Leu-Arg-Asn-Pro-NH2 是一种具备生物活性的肽。研究凝血酶受体束缚配体 SFLLRNP 的结构活性表明,Phe-2-苯基在受体识别过程中具有关键作用。研究还发现,将 Phe-2 替换为对氟苯丙氨酸 [(pF)Phe],可以提升其生物活性。 | |||
TP2212 |
a-MSH, amide
|
Others | Others |
a-MSH, amide is a peptide with the sequence Ac-Ser-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2, MW= 1664.9. The melanocyte-stimulating hormones (collectively referred to as MSH or intermedins) are a class of peptide hormones that are produced by c |