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Results for "

achn

" in TargetMol Product Catalog
  • Inhibitor Products
    14
    TargetMol | Activity
  • Natural Products
    4
    TargetMol | inventory
ACHN-975 TFA
T102361410809-37-8In house
ACHN-975 TFA is a selective LpxC inhibitor with a subnanomolar inhibitory. It is against a wide range of gram-negative bacterias with low MIC values (≤1 μg/mL).
  • $1,100
10-14 weeks
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TargetMol | Inhibitor Sale
ACHN-975
T10236L1410809-36-7
ACHN-975 is a highly potent and selective LpxC inhibitor, demonstrating subnanomolar inhibitory activity. It effectively targets a broad spectrum of gram-negative bacteria, with low minimum inhibitory concentration (MIC) values (≤1 μg/mL)[1].
  • $2,870
10-14 weeks
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Lachnone A
T81963903892-99-9
Lachnone A, a chromone derivative, has been isolated from the filamentous fungus Lachnum sp. BCC 2424 [1].
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Lachnanthocarpone
T3252328241-21-6
Lachnanthocarpone is a member of the 6-oxygenated phenylphenalenones.
  • $1,520
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Tetrahydrolachnophyllum lactone
TN513256407-87-5
Tetrahydrolachnophyllum lactone is a natural product for research related to life sciences. The catalog number is TN5132 and the CAS number is 56407-87-5.
  • $520
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(Z)-Lachnophyllum lactone
TN580381122-95-4
(Z)-Lachnophyllum lactone is a natural product for research related to life sciences. The catalog number is TN5803 and the CAS number is 81122-95-4.
  • $460
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Cyclostachnine
T131505
Cyclostachnine is a useful organic compound for research related to life sciences and the catalog number is T131505.
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AUZ 454
T6866853299-07-7
AUZ 454 (K03861) is a type II CDK2 inhibitor with Kd of 50 nM, 18.6 nM, 15.4 nM, and 9.7 nM for CDK2(WT), CDK2(C118L), CDK2(A144C), and CDK2(C118L/A144C), respectlvely.
  • $31
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TargetMol | Citations Cited
IT-143B
T38385183485-34-9
IT-143B is a bacterial metabolite that has been found in S. iakyrus.1 It inhibits the proliferation of OS-RC-2 and ACHN cancer cells (IC50s = 22 and 98 μM, respectively). |1. Li, K., Liang, Z., Chen, W., et al. Iakyricidins A-D, antiproliferative piericidin analogues bearing a carbonyl group or cyclic skeleton from Streptomyces iakyrus SCSIO NS104. J. Org. Chem. 84(19), 12626-12631 (2019).
  • $1,133
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Anticancer agent 139
T78780
Compound 6h (Anticancer Agent 139) exhibits potent anticancer activity, engaging in a π-cationic interaction with Lys352 of Tubulin and demonstrating high efficacy against SNB-19, OVCAR-8, and NCI-H460 with PGIs of 86.61, 85.26, and 75.99, respectively. Moreover, it shows moderate activity against a range of other cancer cell lines — HOP-62, SNB-75, ACHN, NCI/ADR-RES, 786-O, A549/ATCC, HCT-116, and MDA-MB-231 — with PGIs between 51.88 and 67.55 [1].
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Fenoldopam mesylate
T683567227-57-0
Fenoldopam mesylate (Corlopam mesylate) is a selective dopamine-1 receptor (DA1) agonist with natriuretic/diuretic properties. It lowers blood pressure through arteriolar vasodilation.
  • $43
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DIM-C-pPhOH
T4400151358-47-3
DIM-C-pPhOH (CDIM8) is a nur77 (NR4A1) antagonist,inhibits TGF-β induced cell migration of breast cancer cell lines,promotes ROS/endoplasmic reticulum stress and proapoptotic pathways in pancreatic cancer cell lines,mimics effects of Nur77 RNAi silencing.
  • $37
In Stock
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Gramicidin A
T3643911029-61-1
Gramicidin A is a peptide antibiotic isolated from B. brevis.Gramicidin A is a highly hydrophobic channel-forming ion carrier that forms monovalent cation-permeable channels in artificial membranes.Gramicidin A induces the degradation of hypoxia-inducible factor 1 alpha (HIF-1 alpha) and reduces the growth of a mouse xenograft model of human renal cell carcinoma. Gramicidin A has antibacterial, antimalarial and hemolytic activities.
  • $78
35 days
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4SC-207
T68480871015-11-1
4SC-207 is a novel microtubule inhibitor , which shows strong anti-proliferative activity in a large panel of tumor cell lines with an average GI50 of 11 nM. In particular, 4SC-207 is active in multi-drug resistant cell lines, such as HCT-15 and ACHN, suggesting that it is a poor substrate for drug efflux pumps. 4SC-207 inhibits microtubule growth in vitro and in vivo and promotes, in a dose dependent manner, a mitotic delay/arrest, followed by apoptosis or aberrant divisions due to chromosome alignment defects and formation of multi-polar spindles. Furthermore, preliminary data from preclinical studies suggest low propensity towards bone marrow toxicities at concentrations that inhibit tumor growth in paclitaxel-resistant xenograft models. 4SC-207 may be a potential anti-cancer agent.
  • $1,520
6-8 weeks
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