Tetrapyrroles and derivatives
Frontier Specialty Chemicals 1G MESO-TETRA(P-HYDROXYPHENYL)
meso-Tetra(p-hydroxyphenyl)porphine; CAS: 51094-17-8; 1g
Frontier Specialty Chemicals 250MG MESO-TETRA(PENTAFLUOROPH
This item has a minimum qty of 2 per supplier requirements.
meso-Tetra(pentafluorophenyl)porphine chlorin free; CAS: 25440-14-6; 250mg
Strem, An Ascensus Company CAS# 14609-54-2. 1g. meso-Tetra(4-carboxyphenyl)porphine, 98%. MFCD00064860
CAS# 14609-54-2. 1g. meso-Tetra(4-carboxyphenyl)porphine, 98%. MFCD00064860. Molecular Weight: 790.79. Molecular Formula: C48H30N4O8. Color/form: purple pwdr. Strem# 07-1970. http://www.strem.com/catalog/v/07-1970/
Selleck Chemical LLC Protoporphyrin IX (PPIX) S5145-25mg
Protoporphyrin IX (PPIX) is a heterocyclic organic compound which consists of four pyrrole rings and is the final intermediate in the heme biosynthetic pathway
Selleck Chemical LLC Protoporphyrin IX (PPIX) S5145-1g
Protoporphyrin IX (PPIX) is a heterocyclic organic compound which consists of four pyrrole rings and is the final intermediate in the heme biosynthetic pathway
Cayman Chemical Mn III ProtoporphyrIn IX Chl
A broad-spectrum synthetic fluoroquinolone antibiotic active against Gram-negative and Gram-positive bacteria including clinical isolates of E coli K pneumoniae methicillin-susceptible and -resistant S aureus and methicillin-susceptible and -resistant S epidermidis (MIC90s 0 05 0 1 0 39 12 5 0 39 and 6 25 g/ml respectively) inhibits E coli P aeruginosa and S aureus DNA gyrase (IC50s 0 88 1 9 and 10 2 g/ml respectively) and S aureus topoisomerase IV (IC50 24 2 g/ml) in cell-free assays active against systemic E coli K pneumoniae and methicillin-resistant S aureus infections in mice (ED50s 0 15 5 5 and 4 5 mg/kg respectively)
Cayman Chemical ZInc ProtoporphyrIn-9 10mg
A biotinylating reagent that contains two aminohexanoic spacers to increase the efficiency of avidin-binding by alleviating steric hindrance
Abcam P5091, USP-7 inhibitor, 25MG
MW 348.2 Da, Purity >98%. Potent, selective and cell-permeable USP-7 inhibitor (EC₅₀ = 4.2 μM). Induces apoptosis in cancer cells in vitro. Antiangiogenic and antitumor agent. Active in vitro and in vivo.
The product is subject to the following: Abcam Restricted Use Statement
Abcam (R)-CPP (mM/ml), NMDA antagonist, 10MM_ML
MW 252.2 Da. Highly potent, competitive NMDA antagonist; more active enantiomer of (RS)-CPP (ab120160). (Ki values are 0.04, 0.3, 0.6 and 2.0 μM at NR1/NR2A, NR1/NR2B, NR1/NR2C and NR1/NR2D, respectively).
The product is subject to the following: Abcam Restricted Use Statement
Abcam 4-Thiouridine, RNA synthesis inhibitor, 100MG
MW 260.27 Da, Purity >99%. Ribonucleoside (Uridine ab143255) analog. Antisense agent. RNA synthesis inhibitor. Modifies oligos slated for RNA. Induces p53 and inhibits proliferation. Metabolically labels RNA for stability studies.
The product is subject to the following: Abcam Restricted Use Statement
Abcam AT x -II, NaV channel activator, 100UG
MW 4941 Da, Purity >95%. ATX-II, NaV channel activator. Achieve your results faster with highly validated, pure and trusted compounds.
The product is subject to the following: Abcam Restricted Use Statement
Abcam Latrunculin A (LAT-A), Actin polymerization inhibitor, 100UG
MW 421.6 Da, Purity >95%. Actin polymerization inhibitor. Potent antiproliferative agent. Stabilizes monomeric G-actin. Shows greater potency than Latrunculin B (ab144291). Binds actin monomers near the nucleotide binding cleft with 1:1 stoichiometry. Inhibits growth of cancer cell lines (IC₅₀ values are 142, 142, 142, 166 and 95 nM for A549, H522-T1, HT-29, U-937 and MDA-MB-43 cells respectively). Shows convulsant effects in vivo. .
The product is subject to the following: Abcam Restricted Use Statement
Abcam Latrunculin A (LAT-A), Actin polymerization inhibitor, 500UG
MW 421.6 Da, Purity >95%. Actin polymerization inhibitor. Potent antiproliferative agent. Stabilizes monomeric G-actin. Shows greater potency than Latrunculin B (ab144291). Binds actin monomers near the nucleotide binding cleft with 1:1 stoichiometry. Inhibits growth of cancer cell lines (IC₅₀ values are 142, 142, 142, 166 and 95 nM for A549, H522-T1, HT-29, U-937 and MDA-MB-43 cells respectively). Shows convulsant effects in vivo. .
The product is subject to the following: Abcam Restricted Use Statement
Abcam CL-316243 disodium salt, adrenergic-beta3 receptor agonist, 25MG
MW 465.8 Da, Purity >99%. Selective adrenergic-β3 receptor agonist. Induces adipose tissue remodelling in rat. Hypoglycemic agent. Active *in vivo* and *in vitro*.
The product is subject to the following: Abcam Restricted Use Statement