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T11202Enniatin complex；恩镰孢菌素复合物Enniatin complex
Enniatin complex, a mixture of cyclohexadepsipeptides predominantly derived from various Fusarium species of fungi, exhibits inhibitory effects on enzymes such as acyl-CoA: cholesterol acyl transferase. Furthermore, it has demonstrated the ability to induce apoptosis in multiple cancer cell lines. In addition to these activities, the Enniatin complex possesses ionophoric, antibiotic, and in vitro hypolipidemic properties.
价 格：￥电议型 号：T11202产 地：中国大陆
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T11200Endoxifen (E-isomer)；N-去甲-4-羟基-三苯氧胺E-Endoxifen|||Endoxifen E-isomer；N-去甲-4-羟基-三苯氧胺|||E-Endoxifen|||E
Endoxifen E-isomer (E-Endoxifen) is the E-isomer of (Z)-Endoxifen. Endoxifen E-isomer has antiestrogenic effects.
价 格：￥电议型 号：T11200产 地：中国大陆
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T1120Dacarbazine；达卡巴嗪Imidazole Carboxamide|||DTIC-Dome；Imidazole Carboxamide|||达卡巴嗪|||DTIC-Dome
Dacarbazine (DTIC-Dome) is an antineoplastic agent. It has significant activity against melanomas.
价 格：￥电议型 号：T1120产 地：中国大陆
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T11198Endomorphin 2 TFA；内吗啡肽 2 三氟乙酸盐Endomorphin 2 TFA
Endomorphin 2 TFA, displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM. a high affinity, highly selective agonist of the μ-opioid receptor,
价 格：￥电议型 号：T11198产 地：中国大陆
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T11197Enclomiphene D4 hydrochloride；化合物 T11197(E)-Clomiphene D4 hydrochloride|||Enclomifene D4 hydrochlori
Enclomiphene D4 hydrochloride ((E)-Clomiphene D4 hydrochloride; trans-Clomiphene D4 hydrochloride; Enclomifene D4 hydrochloride) is a potent and orally active oestrogen receptor antagonist, with antioestrogenic property.Enclomiphene D4 hydrochloride ((E)-Clomiphene D4 hydrochloride; trans-Clomiphene D4 hydrochloride; Enclomifene D4 hydrochloride) is a deuterium labeled Enclomiphene.
价 格：￥电议型 号：T11197产 地：中国大陆
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T11195Enantiomer of Sofosbuvir；化合物 T11195Enantiomer of Sofosbuvir
Sofosbuvir´s enantiomer, a variant of the prescription medication Sofosbuvir used for chronic hepatitis C treatment, currently lacks reported biological activity.
价 格：￥电议型 号：T11195产 地：中国大陆
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T11173LElacestrant S enantiomer dihydrochloride；化合物 T11173LRAD1901 S enantiomer dihydrochloride|||RAD-1901
Elacestrant (RAD1901) dihydrochloride is a selective and orally available estrogen receptor (ERR) degrader with IC50 values of 48 and 870 nM for ERα and ERβ, respectively. Elacestrant S enantiomer dihydrochloride is an low activity enantiomer of elacestrant dihydrochloride.
价 格：￥电议型 号：T11173L产 地：中国大陆
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T11173Elacestrant S enantiomer；化合物 T11173RAD1901 S enantiomer；RAD1901 S enantiomer
Elacestrant S enantiomer is a selective and orally available estrogen receptor (ERR) degrader with IC50 values of 48 and 870 nM for ERα and ERβ, respectively.
价 格：￥电议型 号：T11173产 地：中国大陆
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T11156Nazartinib S-enantiomer；化合物 T11156EGF816 (S-enantiomer)；EGF816 (S-enantiomer)
Nazartinib is an EGFR inhibitor. Nazartinib S-enantiomer is the less active S-enantiomer of Nazartinib.
价 格：￥电议型 号：T11156产 地：中国大陆
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T11129LDuvelisib (R enantiomer) hydrochloride；杜韦利西布R对映体盐酸盐IPI-145 R enantiomer HCl|||Duvelisib (R enantiome
Duvelisib (R enantiomer) hydrochloride (INK1197 R enantiomer HCl) is a PI3K inhibitor. Duvelisib (R enantiomer) hydrochloride is the less active enantiomer of Duvelisib.
价 格：￥电议型 号：T11129L产 地：中国大陆
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T11129Duvelisib (R enantiomer)化合物Duvelisib R entiomerDuvelisib R enantiomer|||IPI-145 R enantiomer|||INK11
Duvelisib R enantiomer (IPI-145 R enantiomer) is an enantiomer of Duvelisib with lower activity. Duvelisib is a PI3K inhibitor.
价 格：￥电议型 号：T11129产 地：中国大陆
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T110951Compound F0447-0245；化合物 F0447-0245Compound F0447-0245
Antitubercular agent-33 is a 2-aminothiazole derivative with potent anti-tubercular activity against Mycobacterium tuberculosis ( Mtb ) [1].
价 格：￥电议型 号：T110951产 地：中国大陆
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T11044Dihydromunduletone化合物DihydromunduletoneDHM
Dihydromunduletone (DHM) is an adhesion G protein-coupled receptor (aGPCR) antagonist that acts as a chemical probe for the inhibition of GPR56 and GPR114/ADGRG5, which have similar tethered agonists.
价 格：￥电议型 号：T11044产 地：中国大陆
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T11041Dihydro-β-erythroidine hydrobromide；化合物 T11041DHβE hydrobromide；DHβE hydrobromide
Dihydro-β-erythroidine hydrobromide(DHβE) is a potent, oral active and competitive antagonist of neuronal nicotinic acetylcholine receptors (nAChRs). Dihydro-β-carotene hydrobromide showed selectivity to α4β4 and α4β2nAChR, with IC50 of 0.19 and 0.37 μM, respectively.
价 格：￥电议型 号：T11041产 地：中国大陆
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T1104Paromomycin Sulfate；硫酸巴龙霉素Aminosidine sulfate|||Paromomycin sulfate salt；Aminosidine sulfate|||Parom
Paromomycin binds specifically to the RNA oligonucleotide at the A site of bacterial 30S ribosomes, thereby causing misreading and premature termination of translation of mRNA and inhibition of protein synthesis followed by cell death. Paromomycin Sulfate (Aminosidine sulfate) is the sulfate salt form of paromomycin, a structural derivative of neomycin, an aminoglycoside antibiotic with amebicidal and bactericidal effects against predominantly aerobic gram-negative bacteria.
价 格：￥电议型 号：T1104产 地：中国大陆
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T11035diABZI STING agonist-1 (Tautomerism)；化合物T11035diABZI STING agonist (Compound 3)；diABZI STING agonist
diABZI STING agonist-1 (Tautomerism) (diABZI STING agonist (Compound 3)) is a selective stimulator of interferon genes (STING) receptor agonist, with EC50s of 130, 186 nM for human and mouse, respectively.
价 格：￥电议型 号：T11035产 地：中国大陆
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T11010Detomidine carboxylic acid；地托米定羧酸Detomidine carboxylic acid
Detomidine carboxylic acid is the main urine metabolite of detomidine. Detomidine is a synthetic α2-adrenergic agonist and an animal analgesic. Detomidine also has heart and breathing effects, and has a diuretic effect.
价 格：￥电议型 号：T11010产 地：中国大陆
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T11004Desformylflustrabromine hydrochloride；化合物T11004dFBr hydrochloride|||Deformylflustrabromine hydrochlo
Desformylflustrabromine hydrochloride (dFBr hydrochloride) is a selective agonist of nicotinic acetylcholine receptor (nAChR) in α4β2 neurons, with pEC50 of 6.48.
价 格：￥电议型 号：T11004产 地：中国大陆
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T10949D8-MMAF；化合物 T10949Monomethylauristatin F D8；Monomethylauristatin F D8
D8-MMAF is a microtubule destroyer, deuterated form of MMAF.
价 格：￥电议型 号：T10949产 地：中国大陆
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T10948MMAE-d8；化合物 T10948D8-MMAE|||D8-Monomethyl auristatin E；D8-MMAE|||D8-Monomethyl auristatin E
D8-MMAE (D8-Monomethyl auristatin E) is an effective mitotic inhibitor and tubulin inhibitor, deuterated MMAE.
价 格：￥电议型 号：T10948产 地：中国大陆
