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  • T11681Isochondrodendrine；化合物 T11681Isochondrodendrin；Isochondrodendrin

    Isochondodendrine has strong antiplasmodial activity against Plasmodium falciparum. Isochondrodendrine is a class of bisbenzylisoquinoline alkaloid isolated from Isolona ghesquiereina.

    价 格：￥电议型 号：T11681产 地：中国大陆

  • T11680Isoasatone A；异细辛酮 AIsoasatone A

    Isoasatone A acts against S. litura by acting on cytochrome P450 monooxygenase and glutathione transferase. Isoasatone A is a natural product isolated from Heterotropa takaoi M..

    价 格：￥电议型 号：T11680产 地：中国大陆

  • T1168Desonide地索奈德Tridesilon|||地索奈德|||Locapred|||Prednacinolone

    Desonide (Prednacinolone) is a synthetic glucocorticosteroid for topical use, with anti-inflammatory activity. Desonide binds to glucocorticoid receptors in the cytoplasm, and the ligand-receptor complex is translocated as a homodimer into the nucleus, where transcription activation via glucocorticoid response elements within glucocorticoid-responsive genes occur. This agent induces transcription of genes coding for anti-inflammatory proteins, including lipocortin-1, interleukin-10, interleukin-

    价 格：￥电议型 号：T1168产 地：中国大陆

  • T11677Irindalone；化合物 T11677Lu 21-?098；Lu 21-?098

    IrindaloneIrindalone is a potent serotonin (5-HT2) antagonist.

    价 格：￥电议型 号：T11677产 地：中国大陆

  • T11676Iriflophenone 3-C-glucoside；化合物Iriflophenone 3-C-glucosideIriflophenone 3-C-β-D-glucopyranoside；Irif

    Iriflophenone 3-C-glucoside (Iriflophenone 3-C-β-D-glucopyranoside),has antioxidant activity,isolated from Cyclopia genistoides.

    价 格：￥电议型 号：T11676产 地：中国大陆

  • T11675Irbesartan-d4；厄贝沙坦 D4SR-47436 D4|||BMS-186295 D4；厄贝沙坦 D4|||SR-47436 D4|||BMS-186295 D4

    Irbesartan D4, a deuterium-labeled variant of Irbesartan, is a highly potent and specific antagonist of the angiotensin II type 1 (AT1) receptor.

    价 格：￥电议型 号：T11675产 地：中国大陆

  • T11674IRAK4-IN-6；化合物 T11674IRAK4-IN-6

    IRAK4-IN-6 is a selective and orally efficacious inhibitor of IRAK4, demonstrating an IC50 value of 4 nM. This compound specifically targets MyD88 L265P mutant diffuse large B-cell lymphoma [1].

    价 格：￥电议型 号：T11674产 地：中国大陆

  • T11673IRAK4-IN-4；化合物IRAK4-IN-4IRAK4-IN-4

    IRAK4-IN-4 (compound 15) inhibits cyclic GMP-AMP synthase (cGAS) with an IC50 of 2.1 nM.IRAK4-IN-4 is an interleukin-1 receptor–associated kinase 4 (IRAK4) inhibitor, has an IC50 of 2.8 nM.

    价 格：￥电议型 号：T11673产 地：中国大陆

  • T11672IRAK inhibitor 4；化合物 T11672IRAK inhibitor 4

    IRAK inhibitor 4 is an interleukin-1 receptor associated kinase 4 inhibitor.

    价 格：￥电议型 号：T11672产 地：中国大陆

  • T11671IRAK inhibitor 4 trans；化合物 T11671IRAK inhibitor 4 trans

    IRAK inhibitor 4 is a compound that functions as an inhibitor of interleukin-1 receptor-associated kinase 4 (IRAK4). It specifically targets and inhibits the activity of IRAK4. The (trans) form of IRAK inhibitor 4 refers to its specific molecular configuration.

    价 格：￥电议型 号：T11671产 地：中国大陆

  • T11670IRAK inhibitor 3；化合物IRAK inhibitor 3IRAK inhibitor 3

    IRAK inhibitor 3 is an interleukin-1 (IL-1) receptor-associated kinase (IRAK) modulator.

    价 格：￥电议型 号：T11670产 地：中国大陆

  • T1167Cyproterone acetate醋酸环丙孕酮Androcur|||醋酸环丙氯地孕酮|||Cyproterone 17-O-acetate|||醋酸环丙孕酮

    Cyproterone acetate (Cyproterone 17-O-acetate) binds the androgen receptor (AR), thereby preventing androgen-induced receptor activation in target tissues and inhibiting the growth of testosterone-sensitive tumor cells. Cyproterone acetate is the acetate salt of a synthetic steroidal antiandrogen with weak progestational and antineoplastic activities. This agent also exerts progestational agonist properties at the level of the pituitary that reduce luteinizing hormone (LH), resulting in reductio

    价 格：￥电议型 号：T1167产 地：中国大陆

  • T11669IR415；化合物IR415IR415

    IR415 selectively interacts with Hepatitis B virus X protein (HBx, Kd = 2 nM) and blocks HBV-mediated RNAi suppression, reverses the inhibitory effect of HBx protein on the activity of the dicer endoribonuclease. IR415 is a potent anti-HBV agent and inhibits HBV replication by blocking the HBx activity.

    价 格：￥电议型 号：T11669产 地：中国大陆

  • T11668IQB-782；化合物 IQB-782IQB-782

    IQB-782 is a mucolytic agent with mucolytic expectorant activity.IQB-782 inhibits thrombin-activating fibrinolytic inhibitor (TAFI), protects rats from tobacco smoke-induced respiratory obstruction, reduces the viscosity of gastric mucin suspensions in vitro, and may be useful in studies of obstructive lung disease.IQB-782 has been shown to reduce the viscosity of gastric mucin suspensions in vitro.

    价 格：￥电议型 号：T11668产 地：中国大陆

  • T11667Ipragliflozin (L-Proline)化合物 T11667Ipragliflozin L-Proline

    Ipragliflozin is a highly potent and selective SGLT2 inhibitor with an IC50 of 2.8 nM; little and NO potency for SGLT1/3/4/5/6.

    价 格：￥电议型 号：T11667产 地：中国大陆

  • T11666IPR-803；化合物IPR-803IPR-803

    IPR-803 is an effective inhibitor of the uPAR·uPA protein-protein interaction (PPI) with anti-tumor activity. IPR-803 binds directly to uPAR with a Ki of 0.2 μM.

    价 格：￥电议型 号：T11666产 地：中国大陆

  • T11665Ionomycin calcium；罗红霉素钙盐(链霉菌属载体)SQ23377 calcium；SQ23377 calcium|||罗红霉素钙盐(链霉菌属载体)

    lonomycin calcium is a potent, selective calcium ionophore and an antibiotic produced by Streptomyces conglobatus. also induces the activation of protein kinase C (PKC). Ionomycin calcium (SQ23377 calcium) is highly specific for divalent cations (Ca>Mg>Sr=Ba). Ionomycin promotes apoptosis.

    价 格：￥电议型 号：T11665产 地：中国大陆

  • T11664INY-03-041；化合物 T11664INY-03-041

    INY-03-041, a potent and highly selective PROTAC-based pan-AKT degrader, inhibits AKT1, AKT2, and AKT3 with IC50s of 2.0 nM, 6.8 nM, and 3.5 nM, respectively. This compound consists of the ATP-competitive AKT inhibitor GDC-0068 conjugated to Lenalidomide.

    价 格：￥电议型 号：T11664产 地：中国大陆

  • T11663Integrin-IN-2；化合物 T11663Integrin-IN-2

    Integrin-IN-2 is an orally bioavailable pan αv integrin inhibitor.Integrin-IN-2 can increases the αvβ6, αvβ3, αvβ5 and αvβ8 binding affinities with pIC50 values of 7.8, 8.4, 8.4 and 7.4, respectively.

    价 格：￥电议型 号：T11663产 地：中国大陆

  • T11662LINT-777；化合物INT-777S-EMCA；S-EMCA

    INT-777 (S-EMCA) is a potent TGR5 agonist with an EC50 of 0.82 μM. INT-777 (S-EMCA) inhibits NLRP5-ASC inflammasome-mediated neuroinflammation via the TGR3/cAMP/PKA signaling pathway after subarachnoid hemorrhage in rats.

    价 格：￥电议型 号：T11662L产 地：中国大陆

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