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T75770Deltorphin 2 TFA；化合物 Deltorphin 2 TFADeltorphin 2 TFA
Deltorphin 2 TFA is a selective peptide agonist for the δ opioid receptor [1] .
价 格：￥电议型 号：T75770产 地：中国大陆
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T75750Dermaseptin TFA；Dermaseptin TFADermaseptin TFA
Dermaseptin TFA, a peptide isolated from frog skin, exhibits potent antimicrobial activity against?bacteria,?fungi, and?protozoa?at micromolar concentration [1] .
价 格：￥电议型 号：T75750产 地：中国大陆
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T75716Disitertide TFA；化合物 Disitertide TFADisitertide TFA
Disitertide (P144) TFA is a peptide-based inhibitor of transforming growth factor-beta 1 (TGF-β1), specifically engineered to prevent its interaction with the receptor. Additionally, it functions as a PI3K inhibitor and promotes apoptosis, as supported by references [1] [2] [3] [4] [5].
价 格：￥电议型 号：T75716产 地：中国大陆
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T7556Fadrozole hydrochloride；盐酸法倔唑CGS 16949A；CGS 16949A|||盐酸法倔唑
Fadrozole hydrochloride (CGS 16949A) is a model aromatase inhibitor that has been shown to suppress estrogen production in the ovaries of fish.
价 格：￥电议型 号：T7556产 地：中国大陆
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T74412dTAGV-1-NEG TFA；化合物 dTAGV-1-NEG TFAdTAGV-1-NEG TFA
dTAGV-1-NEG TFA, a diastereomer, serves as the heterobifunctional negative control for dTAGV-1. It acts specifically as an FKBP12 F36V-selective degrader [1].
价 格：￥电议型 号：T74412产 地：中国大陆
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T73864Deltasonamide 1 TFA；化合物 Deltasonamide 1 TFADeltasonamide 1 TFA
Deltasonamide 1 TFA functions as a PDE6δ-KRas inhibitor, exhibiting a dissociation constant (K_D) of 203 pM, indicating its high affinity for this target. It is utilized in tumor research [1].
价 格：￥电议型 号：T73864产 地：中国大陆
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T73637Dot1L-IN-1 TFA；化合物 Dot1L-IN-1 TFADot1L-IN-1 TFA
Dot1L-IN-1 TFA is a potent and selective Dot1L inhibitor, characterized by a K i of 2 pM and an IC 50 of <0.1 nM. It effectively inhibits H3K79 dimethylation (IC 50 =3 nM) and suppresses the HoxA9 promoter activity (IC 50 =17 nM) in HeLa and Molm-13 cells, respectively [1].
价 格：￥电议型 号：T73637产 地：中国大陆
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T7197LFadrozole HCl hydrate；化合物 T7197LFadrozole|||CGS-16949A|||Fadrozole hydrochloride hemihydrate|||CGS16
Fadrozole is a selective inhibitor of aromatase. It also effective in the treatment of estrogen-dependent diseases including breast cancer.
价 格：￥电议型 号：T7197L产 地：中国大陆
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T7197Fadrozole；法倔唑Fadrozole
Fadrozole is a nonsteroidal aromatase inhibitor with potential antineoplastic activity(IC50 : 6.4 nM)
价 格：￥电议型 号：T7197产 地：中国大陆
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T71772Bicifadine free base；化合物 Bicifadine free baseCL-220075|||Bicifadine free base|||CL220075|||Bicifadin
Bicifadine, also known as DOV-220075, CL 220,075, is a SNDR inhibitor potentially for the treatment of lower back pain. Bicifadine has a non-opioid, non-NSAID mechanism for the treatment of pain, which should have less abuse potential than opioid drugs and less propensity to cause gastric ulcers than NSAID drugs. While the drug is purported to be a serotonin (SERT) and noradrenaline transporter (NET) inhibitor, it also has effects at the dopamine transporter (DAT), effectively making it a broad
价 格：￥电议型 号：T71772产 地：中国大陆
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T70958Dov-Val-Dil-OH TFA；化合物 Dov-Val-Dil-OH TFADov-Val-Dil-OH TFA
Dov-Val-Dil-OH is a useful chemical intermediate for synthesis of auristatin-related compounds, such as Monomethyl auristatin E (MMAE), Auristatins are antimitotic agents which inhibits cell division by blocking the polymerisation of tubulin.
价 格：￥电议型 号：T70958产 地：中国大陆
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T70542Nafadotride；化合物 NafadotrideNafadotride
Nafadotride is a dopamine D3 receptor antagonist.
价 格：￥电议型 号：T70542产 地：中国大陆
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T70175Fadaltran；化合物 FadaltranFadaltran
Fadaltran is an α2-adrenoreceptor antagonist.
价 格：￥电议型 号：T70175产 地：中国大陆
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T70078Fadolmidine；化合物 FadolmidineFadolmidine
Fadolmidine is a novel and potent alpha2 -adrenoceptor (alpha2) -AR) agonist developed for spinal analgesia.
价 格：￥电议型 号：T70078产 地：中国大陆
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T70077Fadolmidine HCl；化合物 Fadolmidine HClFadolmidine HCl
Fadolmidine, also known as MPV-2426, is a novel and potent alpha2 -adrenoceptor (alpha2) -AR) agonist developed for spinal analgesia. Fadolmidine displayed high affinity and full agonist efficacy at all three human alpha2-adrenoceptor subtypes (A, B and C) in transfected CHO cells with EC50 values (nM) of 0.4, 4.9 and 0.5, respectively. Fadolmidine inhibited also electrically evoked contractions in rat vas deferens demonstrating the activation of rodent presynaptic alpha2D-adrenoceptors with an
价 格：￥电议型 号：T70077产 地：中国大陆
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T6992Sulfadiazine sodium；磺胺嘧啶钠Sulfadiazin-natrium|||Sodium sulfadiazine；Sulfadiazin-natrium|||磺胺嘧啶钠|||Sod
Sulfadiazine sodium (Sulfadiazin-natrium) is a sodium salt form of sulfadiazine, an intermediate-acting bacteriostatic, synthetic sulfanilamide derivative.
价 格：￥电议型 号：T6992产 地：中国大陆
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T69530Difelikefalin TFA；化合物 Difelikefalin TFADifelikefalin TFA
Difelikefalin TFA is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM). Difelikefalin TFA is selective for KOR over the μ-opioid receptor (MOR; EC50 = >1 ?M in a transactivation assay). It reduces acetic acid-induced writhing, as well as scratching behavior induced by the KOR antagonist GNTI, in mice (ED50s = 0.07
价 格：￥电议型 号：T69530产 地：中国大陆
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T65172Flavin adenine dinucleotide；黄素腺嘌呤二核苷酸FAD；FAD
Flavin adenine dinucleotide (FAD) is a REDOX cofactor, a protein cogroup, involved in a variety of metabolic reactions.
价 格：￥电议型 号：T65172产 地：中国大陆
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T64088Lafadofensine (D-(-)-Mandelic acid)；化合物 Lafadofensine (D-(-)-Mandelic acid)Lafadofensine (D-(-)-Mand
Lafadofensine D-(-)-Mandelic acid is a monoamines reuptake inhibitor with adequate effects when administered short-term.
价 格：￥电议型 号：T64088产 地：中国大陆
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T4411DAMGO TFA (78123-71-4(Free base))；化合物DAMGO TFADAMGO TFA (78123-71-4(Free base))
Potent, selective agonist of Mu-opioid receptor. Antinociceptive. Stimulates calcium-activated adenylyl cyclases related cAMP production. Expresses chemokines and chemokine receptors through TGF-beta1. Increases food intake of rats.
价 格：￥电议型 号：T4411产 地：中国大陆
