Furans
Selleck Chemical LLC 1-Aminohydantoin Hydrochloride S4891-25mg
1-Aminohydantoin Hydrochloride is a pharmaceutical and pesticide intermediate
Medchemexpress LLC BMS-911172 10mg | 1644248-18-9 | 339.34 | C16H19F2N3O3 | 10 MG
BMS-911172 is a small-molecule inhibitor of adaptor-associated kinase 1 (AAK1) provided for laboratory research. It has reported nanomolar potency and is offered at high purity for biochemical and cellular studies.
- Selective AAK1 inhibition with nanomolar potency (IC50 ≈ 35 nM).
- High reported purity (≈99.5%).
- Molecular weight 339.34; formula C16H19F2N3O3.
- Soluble in DMSO; solution format available.
- Available in small-scale quantities suitable for research workflows.
- For research use only; not for clinical or human use.
Medchemexpress LLC 21-Hydroxypregnenolone | 1164-98-3 | 98.1% | 332.48 | 10 MG
21-Hydroxypregnenolone is an essential intermediate in corticosterone synthesis.
eMolecules 5-Phenyl-2-furoic acid | 52938-97-3 | MFCD00456304 | 5g
Combi-Blocks | 5-Phenyl-2-furoic acid | 5g | 267187633 | QC-7895 | 95.000 | 52938-97-3 | MFCD00456304 | 188.182 | C11H8O3
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Medchemexpress LLC HY-100578 5mg Medchemexpress, AGK2 CAS:304896-28-4 Purity:>98%
Medchemexpress, HY-100578 5mg AGK2 CAS:304896-28-4 AGK2 is a selective SIRT2 inhibitor with IC 50 of 3.5 μM. AGK2 can also inhibit SIRT1 and SIRT3 with IC 50 of 30 and 91 μM, respectively. 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.
Apexbio Technology LLC Terlipressin diacetate 1884420-36-3 25mg
Terlipressin diacetate (CAS 1884420-36-3) is a synthetic analogue of vasopressin classified as a vasopressin receptor agonist It exhibits high selectivity for V1 receptors localized on vascular smooth muscle where it induces pronounced vasoconstriction by activating the phospholipase C inositol 1 4 5-trisphosphate (IP3) signaling pathway This leads to increased vascular resistance and elevated blood pressure Terlipressin diacetate is widely utilized in biomedical research investigating mechanisms of vascular tone regulation hemodynamic response in portal hypertension and pathophysiology of conditions such as variceal bleeding and hepatorenal syndrome
eMolecules Ethyl 2-furoate | 1335-40-6 | MFCD00003237 | 25g
Combi-Blocks | Ethyl 2-furoate | 25g | 296390685 | OR-1597 | 95.000 | 1335-40-6 | MFCD00003237 | 140.138 | C7H8O3
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Selleck Chemical LLC Dantrolene sodium
Dantrolene sodium(F 440) acts as a postsynaptic muscle relaxant by inhibiting Ca2 ions release from sarcoplasmic reticulum stores by antagonizing ryanodine receptors
TARGETMOL CHEMICALS INC GX-585 1MG
Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. GX-585 is a sulfonamide analog that is a Nav 1.7 channel inhibitor with analgesic activity for the study of neuropathic pain and inflammation. Purity 99.18%
Medchemexpress LLC PF-06456384 trihydrochloride | 1834610-75-1 | 99.4% | 829.18 g/mol | C35H35Cl3F3N7O3S2 | 50 MG
PF-06456384 trihydrochloride is the trihydrochloride salt of a highly potent and selective NaV1.7 inhibitor developed for preclinical pharmacology and pain model research. The compound has been profiled in vitro and in vivo and is supplied as a high-purity research sample.
- Salt form: trihydrochloride.
- Target: voltage-gated sodium channel NaV1.7.
- Potency: IC50 = 0.01 nM against NaV1.7.
- Purity: 99.38% by HPLC (supplier specification).
- Molecular weight: 829.18 g/mol (trihydrochloride salt).
- Molecular formula: C35H35Cl3F3N7O3S2.
- Intended use: preclinical pharmacology and formalin pain model research.
- Supplied quantity: 50 mg research sample.
![Medchemexpress LLC 2-(2-fluorophenyl)-N-hydroxy-2-[4-[5-(trifluoromethyl)pyrimidin-2-yl]phenyl]acetamide | 1629729-98-1 | 98.1% | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000234654.png-250.jpg)
Medchemexpress LLC 2-(2-fluorophenyl)-N-hydroxy-2-[4-[5-(trifluoromethyl)pyrimidin-2-yl]phenyl]acetamide | 1629729-98-1 | 98.1% | 50 MG
CHDI-390576 is a potent, cell-permeable, CNS-penetrant small-molecule inhibitor selective for class IIa histone deacetylases (HDAC4, HDAC5, HDAC7, HDAC9). It is provided as a high-purity research compound for biochemical and cellular studies of HDAC function and selectivity.
- Low-nanomolar inhibitory activity against class IIa HDAC isoforms (reported IC50s: HDAC4 54 nM, HDAC5 60 nM, HDAC7 31 nM, HDAC9 50 nM).
- High selectivity against class I HDACs and over HDAC8 and HDAC6.
- CNS penetrant and cell permeable for central nervous system research.
- High purity suitable for biochemical and cellular assays.
- Molecular formula C19H13F4N3O2; molecular weight 391.32.
Medchemexpress LLC Ganoderal A | 104700-98-3 | 5 MG
Ganoderal A is an oxygenated sterol derived from *Ganoderma lucidum*. It functions as a cholesterol synthesis inhibitor and is intended for research use only.
- Oxygenated sterol derived from *Ganoderma lucidum*.
- Functions as a cholesterol synthesis inhibitor.
- Purity: 97.54%.