Pyrroles
Medchemexpress LLC 8-(4-iodophenyl)-1,3,5,7-tetramethyl BODIPY | 250734-47-5 | 98.5% | 450.07 g·mol⁻¹ | C19H18BF2IN2 | 1 G
8-(4-iodophenyl)-1,3,5,7-tetramethyl BODIPY is an iodinated BODIPY-family fluorescent dye used in research applications as a probe for GFP-labeled muscarinic M1 receptors and for general fluorescent imaging and spectroscopy. It is provided as a high-purity reagent appropriate for laboratory assays, labeling, and microscopy work.
- Iodinated BODIPY fluorophore for fluorescent labeling and imaging.
- Suitable for probing GFP-labeled muscarinic M1 receptors in biological assays.
- High chemical purity (~98%) for reproducible experimental results.
- Molecular weight 450.07 g·mol⁻¹; formula C19H18BF2IN2.
- Typically supplied as a colored solid and stored protected from light at cool temperatures.
eMolecules 23351-07-7 | 4-(1H-Pyrrol-1-yl)benzonitrile | Combi-Blocks | MFCD00085164 | 168.199 | C11H8N2 | 98.000 | N#Cc1ccc(cc1)-n1cccc1 | 1g | 205411941
4-(1H-Pyrrol-1-yl)benzonitrile | Combi-Blocks | 23351-07-7 | MFCD00085164 | 168.199 | C11H8N2 | 98.000 | N#Cc1ccc(cc1)-n1cccc1 | 1g | 205411941
eMolecules 181288-96-0 | 2-Bromo-5-chloro-4-fluorophenol | Apollo Scientific | MFCD28734033 | 225.440 | C6H3BrClFO | 95.000 | Oc1cc(Cl)c(F)cc1Br | 1g | 562459154
2-Bromo-5-chloro-4-fluorophenol | Apollo Scientific | 181288-96-0 | MFCD28734033 | 225.440 | C6H3BrClFO | 95.000 | Oc1cc(Cl)c(F)cc1Br | 1g | 562459154
eMolecules 1313593-59-7 | (1S)-1-(3-CHLORO-3-FLUOROPHENYL)ETHYLAMINE-HCL | MFCD12758016 | 1g
Medchem Express | Ibrutinib-d5 | 1mg | 716993492 | HY-10997S | 1553977-17-5 | 445.538 | C25H24N6O2
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eMolecules 1261851-55-1 | 4-DIFLUOROMETHOXY-3-FLUOROPHENYLACETIC ACID | AstaTech | MFCD18395038 | 220.147 | C9H7F3O3 | 95.000 | OC(=O)Cc1ccc(OC(F)F)c(F)c1 | 1g | 164730171
4-DIFLUOROMETHOXY-3-FLUOROPHENYLACETIC ACID | AstaTech | 1261851-55-1 | MFCD18395038 | 220.147 | C9H7F3O3 | 95.000 | OC(=O)Cc1ccc(OC(F)F)c(F)c1 | 1g | 164730171
eMolecules 2246736-67-2 | ChemScene | 2-(3-((4-Bromo-2-fluorophenoxy)methyl)phenyl)-4455-tetramethyl-132-dioxaborolane | 100mg | 712788379 | CS-0379293 | 407.09 | C19H21BBrFO3
Ambeed | 2-(4-Iodophenyl)acetonitrile | 5g | 525057301 | A146276 | 51628-12-7 | MFCD00060306 | 243.047 | C8H6IN
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Cayman Chemical N-desethyl SunItInIb 10mg
An active metabolite of sunitinib; formed when sunitinib undergoes N-de-ethylation by CYP3A4; is pharmacologically active having similar inhibitory activity to sunitinib
AdipoGen Sunitinib . malate (25 mg)
Chemical. CAS: 341031-54-7. Formula: C22H27FN4O2 . C4H6O5. MW: 398.5 . 134.1. Potent ATP-competitive and cell permeable multi-targeted receptor tyrosine kinase (RTK) inhibitor targeting VEGFR and PDGFR-beta. Inhibits FLK1 (Ki=9nM), PDGFRbeta (Ki=8nM) and FLT3. It is at least 10-fold selective for FLK1 and PDGFRbeta over a variety of tyrosine kinases in a panel, including EGFR, Cdk2, Met, IGFR-1, Abl and Src. Inhibits the cellular receptor phosphorylation of FLT3, RET and CSF-1R. Also shown to inhibit c-Kit. Exhibits potent antiangiogenic and antitumor activity in multiple xenograft models.
Medchemexpress LLC Almotriptan (malate) | 181183-52-8 | 99.5% | 25 MG
Almotriptan malate is an orally active, highly selective 5-HT1B/1D-receptor agonist. It is utilized in research for treating migraine, inducing intracranial vasoconstriction, suppressing vasoactive peptides from trigeminal nerve endings, and inhibiting nociceptive neurotransmission in the trigeminocervical complex. This compound shows low nanomolar affinity for 5-HT1B and 5-HT1D receptors.
- Highly selective 5-HT1B/1D-receptor agonist
- Induces intracranial vasoconstriction
- Suppresses vasoactive peptide release
- Inhibits nociceptive neurotransmission
- Exhibits low nanomolar affinity for 5-HT1B and 5-HT1D receptors
- Has a mild antiemetic effect
- Shows a slight, transient diuretic effect
Cayman Chemical SBromoenol lactone
A selective iPLA2β inhibitor; inhibits vasopressin-induced release of arachidonate from cultured rat aortic smooth muscle (A10) cells (IC50 = 2 µM); >1,000-fold selective for iPLA2 versus cPLA2 and 10-fold selective for iPLA2β versus iPLA2γ
Medchemexpress LLC Clebopride malate | 57645-91-7 | 99.4% | 1 ML
Clebopride malate is an orally active dopamine receptor antagonist. It acts on dopamine D2 receptors and exhibits antiemetic and prokinetic effects. This compound is suitable for research into functional gastrointestinal disorders.
- Orally active dopamine receptor antagonist
- Acts on dopamine D2 receptors
- Possesses antiemetic effects
- Exhibits prokinetic effects
- Selectively binds to D2 dopamine receptors and α2 adrenergic receptors
eMolecules 890655-80-8 | Medchem Express | Verdiperstat | 5mg | 441682006 | HY-17646 | 253.32 | C11H15N3O2S
Medchem Express | Verdiperstat | 5mg | 441682006 | HY-17646 | 890655-80-8 | 253.320 | C11H15N3O2S
Medchemexpress LLC HY-112898 5mg Medchemexpress, DC1SMe CAS:501666-85-9 Purity:>98%
Medchemexpress, HY-112898 5mg DC1SMe CAS:501666-85-9 DC1Sme, a DC1 derivative, exhibits IC50 values of 22 pM, 10 pM, 32 pM and 250 pM for Ramos, Namalwa, HL60/s and COLO 205 cancer cells, respectively. DC1, an analogue of the minor groove-binding DNA alkylator CC-1065, is a ADC Cytotoxin. DC1 can be used in synthesis of antibody-drug conjugates for the targeted treatment of cancer. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.