Aminophenoler
Filtrerede søgeresultater
BN82002, MedChemExpress
MedChemExpress BN82002 is a potent, selective and irreversible inhibitor of CDC25 phosphatase family. BN82002 inhibits CDC25A, CDC25B2, CDC25B3, CDC25C CDC25A, and 25C-cat with IC50 values of 2.4, 3.9, 6.3, 5.4, and 4.6 μM, respectively. BN82002 displays ∼20-fold greater selectivity over CD45 tyrosine phosphatase.
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| Kemisk navn eller materiale | BN82002 |
|---|---|
| Formel vægt | 359.42 |
| Opløselighedsinformation | DMSO : ≥ 150 mg/mL (417.34 mM) |
| Fysisk form | Solid |
| Farve | Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 359.42 |
| CAS | 396073-89-5 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | OC1=C(CN(C)CCC2=CC=C([N+]([O-])=O)C=C2)C=C(N(C)C)C=C1OC |
| Renhedsgrad noter | Research |
| Molekylær formel | C19H25N3O4 |
| Til brug med (applikation) | Cancer-programmed cell death |
ZL0420, MedChemExpress
MedChemExpress ZL0420 is a potent and selective bromodomain-containing protein 4 (BRD4) inhibitor with IC50 values of 27 nM against BRD4 BD1 and 32 nM against BRD4 BD2.
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| Kemisk navn eller materiale | ZL0420 |
|---|---|
| Formel vægt | 296.32 |
| Opløselighedsinformation | DMSO : 125 mg/mL (421.84 mM; Need ultrasonic) |
| Procent renhed | 98.0% |
| Fysisk form | Solid |
| Farve | Orange |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 296.32 |
| CAS | 2230496-80-5 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | OC1=CC(N)=C(/N=N/C2=CC(CCC(N3)=O)=C3C=C2)C=C1C.[(E)] |
| Renhedsgrad noter | Research |
| Molekylær formel | C16H16N4O2 |
| Til brug med (applikation) | COVID-19-immunoregulation |
OTS514, MedChemExpress
MedChemExpress OTS514 is a highly potent TOPK inhibitor with an IC50 of 2.6 nM. OTS514 strongly suppresses the growth of TOPK-positive cancer cells. OTS514 induces cell cycle arrest and apoptosis.
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| Kemisk navn eller materiale | OTS514 |
|---|---|
| Formel vægt | 364.46 |
| Opløselighedsinformation | DMSO : 100 mg/mL (274.38 mM; Need ultrasonic) |
| Procent renhed | 98.15% |
| Fysisk form | Solid |
| Farve | Earth Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 364.46 |
| CAS | 1338540-63-8 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C1NC2=C(C(C3=CC=C([C@@H](C)CN)C=C3)=C(O)C=C2C)C4=C1SC=C4 |
| Renhedsgrad noter | Research |
| Molekylær formel | C21H20N2O2S |
| Til brug med (applikation) | Cancer-Kinase/protease |
inS3-54A18, MedChemExpress
MedChemExpress inS3-54A18 is a potent STAT3 inhibitor, with anti-cancer properties.
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| Kemisk navn eller materiale | inS3-54A18 |
|---|---|
| Formel vægt | 373.83 |
| Opløselighedsinformation | DMSO : ≥ 150 mg/mL (401.25 mM) |
| Procent renhed | 99.83% |
| Fysisk form | Solid |
| Farve | Orange |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 373.83 |
| CAS | 328998-53-4 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C1N(C2=CC=C(O)C=C2)C(C3=CC=CC=C3)=C/C1=C/C4=CC=C(Cl)C=C4 |
| Renhedsgrad noter | Research |
| Molekylær formel | C23H16ClNO2 |
| Til brug med (applikation) | Cancer-Kinase/protease |
Lavendustin A, MedChemExpress
MedChemExpress Lavendustin A (RG-14355), isolated from Streptomyces Griseolavendus, is a potent, specific and ATP-competitive inhibitor of tyrosine kinase, with an IC50 of 11 ng/mL for EGFR-associated tyrosine kinase. It suppresses VEGF-induced angiogenesis and blocks the induction of LTPGABA-A.
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| Kemisk navn eller materiale | Lavendustin A |
|---|---|
| Formel vægt | 381.38 |
| Opløselighedsinformation | DMSO : ≥ 250 mg/mL (655.51 mM) |
| Procent renhed | 95.0% |
| Fysisk form | Solid |
| Farve | Off-White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 381.38 |
| CAS | 125697-92-9 |
| Synonym | RG-14355 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(O)C1=CC(N(CC2=CC(O)=CC=C2O)CC3=CC=CC=C3O)=CC=C1O |
| Renhedsgrad noter | Research |
| Molekylær formel | C21H19NO6 |
| Til brug med (applikation) | Cancer-Kinase/protease |
Acetaminophen metabolite 3-hydroxy-acetaminophen, MedChemExpress
MedChemExpress 3-hydroxy-acetaminophen is a metabolite of Acetaminophen, which is a pain medicine.
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| Kemisk navn eller materiale | Acetaminophen metabolite 3-hydroxy-acetaminophen |
|---|---|
| Sundhedsfare 1 | H302∣H315∣H319∣H335 |
| Formel vægt | 167.16 |
| Opløselighedsinformation | DMSO : 250 mg/mL (1495.57 mM; Need ultrasonic) |
| Procent renhed | 99.03% |
| Fysisk form | Solid |
| Farve | Gray |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 167.16 |
| CAS | 37519-14-5 |
| Synonym | 3-Hydroxyacetaminophen |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | OC1=C(O)C=C(NC(C)=O)C=C1 |
| Renhedsgrad noter | Research |
| Molekylær formel | C8H9NO3 |
| Til brug med (applikation) | Neuroscience-Neuromodulation |
Balsalazide, MedChemExpress
MedChemExpress Balsalazide could suppress colitis-associated carcinogenesis through modulation of IL-6/STAT3 pathway.
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| Kemisk navn eller materiale | Balsalazide |
|---|---|
| Formel vægt | 357.32 |
| Opløselighedsinformation | DMSO : 100 mg/mL (279.86 mM; Need ultrasonic) |
| Procent renhed | 99.2% |
| Fysisk form | Solid |
| Farve | Orange |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 357.32 |
| CAS | 80573-04-2 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(O)C1=CC(/N=N/C2=CC=C(C(NCCC(O)=O)=O)C=C2)=CC=C1O |
| Renhedsgrad noter | Research |
| Molekylær formel | C17H15N3O6 |
| Til brug med (applikation) | COVID-19-immunoregulation |
SKI II, MedChemExpress
MedChemExpress SKI-II is an oral active and synthetic inhibitor of sphingosine kinase (SK) activity, with IC50 values of 78 μM and 45 μM for SK1 and for SK2, respectively. SKI II causes an irreversible inhibition of SK1 by inducing its lysosomal and/or proteasomal degradation.
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| Kemisk navn eller materiale | SKI II |
|---|---|
| Sundhedsfare 1 | H302 |
| Formel vægt | 302.78 |
| Opløselighedsinformation | DMSO : ≥ 100 mg/mL (330.27 mM) |
| Procent renhed | 99.88% |
| Fysisk form | Solid |
| Farve | White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 302.78 |
| CAS | 312636-16-1 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | OC1=CC=C(NC2=NC(C3=CC=C(Cl)C=C3)=CS2)C=C1 |
| Renhedsgrad noter | Research |
| Molekylær formel | C15H11ClN2OS |
| Til brug med (applikation) | Cancer-Kinase/protease |
Propyl pyrazole triol, MedChemExpress
MedChemExpress Propyl pyrazole triol (PPT) is a selective estrogen receptor alpha (ERα) agonist. The relative binding affinity of Propyl pyrazole triol for ERα (ERα: 49%) around 410 times higher compared with estrogen receptor beta (ERβ: 0.12%).
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S55746, MedChemExpress
MedChemExpress S55746 (BCL201) is a potent, orally active and selective BCL-2 inhibitor, with a Ki of 1.3 nM and a Kd of 3.9 nM. S55746 (BCL201) has antitumor activity with low toxicity.
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| Kemisk navn eller materiale | S55746 |
|---|---|
| Formel vægt | 710.82 |
| Opløselighedsinformation | DMSO : 50 mg/mL (70.34 mM; Need ultrasonic) |
| Procent renhed | 98.93% |
| Fysisk form | Powder |
| Farve | Light Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 710.82 |
| CAS | 1448584-12-0 |
| Synonym | BCL201 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(C1=C2CCCCN2C(C3=C(C(N4CC5=C(C=CC=C5)C[C@H]4CN6CCOCC6)=O)C=C(OCO7)C7=C3)=C1)N(C8=CC=C(O)C=C8)C9=CC=CC=C9 |
| Renhedsgrad noter | Research |
| Molekylær formel | C43H42N4O6 |
| Til brug med (applikation) | Cancer-programmed cell death |
Osalmid, MedChemExpress
MedChemExpress Osalmid is a ribonucleotide reductase small subunit M2 (RRM2) targeting compound; suppresses ribonucleotide reductase activity with an IC50 of 8.23 μM.
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| Kemisk navn eller materiale | Osalmid |
|---|---|
| Sundhedsfare 1 | H302∣H315∣H319 |
| Formel vægt | 229.23 |
| Opløselighedsinformation | DMSO : ≥ 100 mg/mL (436.24 mM) |
| Procent renhed | 99.85% |
| Fysisk form | Solid |
| Farve | Off-White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 229.23 |
| CAS | 526-18-1 |
| Synonym | Oxaphenamide 4'-Hydroxysalicylanilide |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(NC1=CC=C(O)C=C1)C2=CC=CC=C2O |
| Renhedsgrad noter | Research |
| Molekylær formel | C13H11NO3 |
| Til brug med (applikation) | COVID-19-anti-virus |
Fenretinide, MedChemExpress
MedChemExpress Fenretinide (4-HPR) is a synthetic retinoid deriverative, binding to the retinoic acid receptors (RAR) at concentrations necessary to induce cell death.
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| Kemisk navn eller materiale | Fenretinide |
|---|---|
| Sundhedsfare 1 | H302+H312+H332∣H315∣H319∣H335∣H360 |
| Formel vægt | 391.55 |
| Opløselighedsinformation | DMSO : ≥ 130 mg/mL (332.01 mM) |
| Procent renhed | 99.08% |
| Fysisk form | Solid |
| Farve | Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 391.55 |
| CAS | 65646-68-6 |
| Synonym | 4-HPR |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | CC(/C=C/C=C(/C=C/C1=C(CCCC(C)1C)C)C)=C\C(NC2=CC=C(O)C=C2)=O |
| Renhedsgrad noter | Research |
| Molekylær formel | C26H33NO2 |
| Til brug med (applikation) | Cancer-programmed cell death |
S55746 hydrochloride, MedChemExpress
MedChemExpress S55746 hydrochloride (BCL201 hydrochloride) is a potent, orally active and selective BCL-2 inhibitor, with a Ki of 1.3 nM and a Kd of 3.9 nM. S55746 hydrochloride (BCL201 hydrochloride) has antitumor activity with low toxicity.
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| Kemisk navn eller materiale | S55746 hydrochloride |
|---|---|
| Formel vægt | 747.28 |
| Opløselighedsinformation | DMSO : 200 mg/mL (267.64 mM; Need ultrasonic) |
| Procent renhed | 98.69% |
| Fysisk form | Powder |
| Farve | Light Yellow |
| Grad | Research |
| Anbefalet opbevaring | 4°C, stored under nitrogen∣In solvent : -80°C, 6 months∣-20°C, 1 month (stored under nitrogen) |
| Molekylvægt (g/mol) | 747.28 |
| CAS | 1448525-91-4 |
| Synonym | BCL201 hydrochloride |
| Holdbarhed | 4°C, stored under nitrogen∣In solvent : -80°C, 6 months∣-20°C, 1 month (stored under nitrogen) |
| SMIL | O=C(C1=C2CCCCN2C(C3=C(C(N4CC5=C(C=CC=C5)C[C@H]4CN6CCOCC6)=O)C=C(OCO7)C7=C3)=C1)N(C8=CC=C(O)C=C8)C9=CC=CC=C9.Cl |
| Renhedsgrad noter | Research |
| Molekylær formel | C43H43ClN4O6 |
| Til brug med (applikation) | Cancer-programmed cell death |
5-Lipoxygenase-In-1, MedChemExpress
MedChemExpress 5-Lipoxygenase-In-1 is a 5-Lipoxygenase inhibitor extracted from patent EP 331232 A2, table 4, compound example 4.10.
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| Kemisk navn eller materiale | 5-Lipoxygenase-In-1 |
|---|---|
| Formel vægt | 424.56 |
| Opløselighedsinformation | DMSO : 250 mg/mL (588.84 mM; Need ultrasonic) |
| Procent renhed | 98.07% |
| Fysisk form | Solid |
| Farve | Off-White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 424.56 |
| CAS | 125235-15-6 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(C(C)(C)N1CC)N(C2=CC=C(N3CCN(C4=CC=C(O)C=C4)CC3)C=C2)C1=S |
| Renhedsgrad noter | Research |
| Molekylær formel | C23H28N4O2S |
| Til brug med (applikation) | COVID-19-immunoregulation |
JANEX-1, MedChemExpress
MedChemExpress JANEX-1 (WHI-P131) is a potent and specific JAK3 inhibitor (estimated Ki=2.3 μM). JANEX-1 (WHI-P131) shows potent JAK3-inhibitory activity (IC50 of 78 μM), does not inhibit JAK1 and JAK2.
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| Kemisk navn eller materiale | JANEX-1 |
|---|---|
| Sundhedsfare 1 | H302∣H315∣H319∣H335 |
| Formel vægt | 297.31 |
| Opløselighedsinformation | DMSO : ≥ 100 mg/mL (336.35 mM) |
| Procent renhed | 99.6% |
| Fysisk form | Solid |
| Farve | Gray |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 297.31 |
| CAS | 202475-60-3 |
| Synonym | WHI-P131 Jak3 inhibitor I |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | OC1=CC=C(NC2=C3C=C(OC)C(OC)=CC3=NC=N2)C=C1 |
| Renhedsgrad noter | Research |
| Molekylær formel | C16H15N3O3 |
| Til brug med (applikation) | Cancer-Kinase/protease |