Alcohols and polyols
- (1)
- (55)
- (347)
- (39)
- (4)
- (8)
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- (55)
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- (1)
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- (153)
- (1)
- (65)
- (27)
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- (1)
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- (30)
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- (20)
- (10)
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- (395)
- (6)
- (102)
- (21)
- (50)
- (31)
- (61)
- (13)
- (14)
- (1)
- (2)
- (1)
- (26)
- (6)
- (4)
- (1)
- (6)
- (1)
- (462)
- (9)
- (46)
- (11)
- (45)
- (6)
- (1)
- (7)
- (10)
- (145)
- (114)
- (6)
- (5)
- (1)
- (1)
- (1)
- (1)
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- (1)
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- (7)
- (14)
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- (1)
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- (5)
- (1)
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- (21)
- (5)
- (2)
- (2)
- (2)
- (16)
- (2)
- (30)
- (2)
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- (1)
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- (20)
- (10)
- (4)
- (15)
- (1)
- (4)
- (6)
- (2)
- (2)
- (2)
- (2)
- (4)
- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
- (5)
- (4)
- (17)
- (15)
- (4)
- (5)
- (2)
- (5)
- (4)
- (33)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (8)
- (7)
- (7)
- (2)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (3)
- (1)
- (15)
- (12)
- (1)
- (2)
- (2)
- (7)
- (12)
- (1)
- (14)
- (24)
- (1)
- (8)
- (4)
- (1)
- (2)
- (1)
- (17)
- (2)
- (6)
- (5)
- (2)
- (1)
- (5)
- (3)
- (4)
- (24)
- (5)
- (3)
- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (7)
- (4)
- (1)
- (1)
- (3)
- (6)
- (11)
- (5)
- (3)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (2)
- (1)
- (3)
- (2)
- (10)
- (1)
- (2)
- (4)
- (4)
- (3)
- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (5)
- (4)
- (1)
- (2)
- (9)
- (4)
- (2)
- (12)
- (4)
- (1)
- (1)
- (5)
- (3)
- (10)
- (2)
- (5)
- (1)
- (1)
- (1)
- (10)
- (5)
- (1)
- (2)
- (2)
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- (1)
- (2)
- (1)
- (1)
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- (1)
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- (1)
- (1)
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- (1)
- (1)
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- (1)
- (1)
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- (1)
- (1)
- (1)
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- (11)
- (1)
- (2)
- (4)
- (20)
- (21)
- (1)
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- (3)
- (3)
- (8)
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- (2)
- (1)
- (1)
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- (9)
- (1)
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- (1)
- (1)
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Filtered Search Results
Medchemexpress LLC Trazodone hydrochloride | 25332-39-2 | 99.9% | 5 MG
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Trazodone hydrochloride is an antidepressant classified as a serotonin receptor antagonist and reuptake inhibitor. It is primarily intended for research and analytical applications, particularly in the study of anxiety disorders, and serves as a reference standard.
- Analytical standard for research
- Used in analytical applications
- Functions as a serotonin receptor antagonist and reuptake inhibitor
- Employed for treatment of anxiety disorders
- Suitable for qualitative, quantitative, and methodological research experiments
- Compatible with HPLC, GC, and MS techniques
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules EMOLECULES INC
5000473237 TERT-BUTYL 3-BROMOPIPERIDIN 5G
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eMolecules EMOLECULES INC
5000473240 TERT-BUTYL 3-BROMOPROPANOAT 1G
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Chemscene ChemScene | 3-Aminocyclohexanol | 1G | CS-W005423 | 0.95 | 6850-39-1| MFCD03790923 | 115.18
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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ChemScene | 3-Aminocyclohexanol | 1G | CS-W005423 | 0.95 | 6850-39-1| MFCD03790923 | 115.18
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Medchemexpress LLC Amelparib hydrochloride | 98.4% | 379.88 | C19H26ClN3O3 | 5 MG
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Amelparib hydrochloride is the hydrochloride salt form of a PARP-1 inhibitor used as a research reagent to investigate DNA damage response and PARP-related pathways. It is supplied as a high-purity solid suitable for biochemical and cellular assays.
- Potent PARP-1 inhibitor activity
- Hydrochloride salt for improved water solubility
- High purity (98.4%)
- Molecular weight 379.88 g/mol
- Suitable for biochemical and cellular research applications
- Supplied as a 5 mg solid package
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eMolecules EMOLECULES INC
5000473545 TERT-BUTYL 2-HYDROXYACETAT 25G
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eMolecules EMOLECULES INC
5000489644 NINHYDRIN 500G
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Matrix Scientific 1-Chloro-6-hydroxyhexane, 2009-83-8, MFCD00002984, 25g
Molecular Formula C6H13ClO, Purity 97%, Molecular Weight 136.62, Boiling Point 108-112/14mm
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Medchemexpress LLC 5α-Pregnane-3β,6α-diol-20-one | 21853-11-2 | ≥98.0% | 334.49 | 50 MG
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5α-Pregnane-3β,6α-diol-20-one is a mitogenic metabolite of progesterone that can be produced in starved androgen-responsive prostate cancer cells. It is formed from progesterone in human fibroblasts and from early steroid precursors in C4.2 cell lines, independently of CYP17A1 but relying on 3β-HSD activity.
- Mitogenic metabolite of progesterone.
- Can be produced in starved androgen-responsive prostate cancer cells.
- Formed from progesterone in human fibroblasts.
- Formed from early steroid precursors in C4.2 cell lines.
- Formation is independent of CYP17A1.
- Formation relies on 3β-HSD activity.
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Medchemexpress LLC Articaine hydrochloride | 23964-57-0 | 99.4% | 1 ML
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Articaine hydrochloride is a selective inhibitor of voltage-gated sodium channels, demonstrating local anesthetic activity by blocking nerve impulse conduction. It also exhibits anti-inflammatory functions by inhibiting NF-κB activation and NLRP3 inflammasome pathways. It is used in the study of dental local anesthesia and inflammatory-related diseases.
- Inhibits voltage-gated sodium channels
- Exhibits local anesthetic activity
- Inhibits NF-κB activation and NLRP3 inflammasome pathways
- Reduces inflammatory factors like TNF-α, IL-6, and IL-1β
- Ameliorates LPS-induced acute kidney injury in animal models
- Can enhance anesthetic effect in zebrafish model
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Sigma Aldrich Fine Chemicals Biosciences N tert Butyl alpha phenyln5G
N tert Butyl alpha phenyln5G
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eMolecules 1-OXA-8-AZASPIRO[4.5]DECAN-2-ONE | 167364-29-6 | MFCD12827982 | 1g
AstaTech | 1-OXA-8-AZASPIRO[4.5]DECAN-2-ONE | 1g | 261436327 | 33494 | 95.000 | 167364-29-6 | MFCD12827982 | 155.197 | C8H13NO2
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Sigma Aldrich Fine Chemicals Biosciences Ruscogenin phyproof(R) Reference Substance | 472-11-7 | MFCD00210550 | 10MG
Ruscogenin phyproof(R) Reference Substance | Purity: >=95.0% (HPLC) | Mol Wt: 430.62 | 472-11-7 | MFCD00210550 | 10MG
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Medchemexpress LLC CHK1-IN-4 hydrochloride | 00-00-0 | 480.75 g/mol | C18H19BrClN7O2 | 5 MG
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CHK1-IN-4 hydrochloride is the hydrochloride salt of a small-molecule inhibitor of checkpoint kinase 1 (CHK1). It is used in preclinical biochemical and cell-based studies to inhibit CHK1 phosphorylation and evaluate antitumor activity. Supplied as a solid with defined solubility and storage recommendations for research use.
- Potent checkpoint kinase 1 (CHK1) inhibitor active in tumor cells.
- Hydrochloride salt form for improved solubility and handling.
- Solid material; soluble in DMSO at 5 mg/mL with ultrasonic and warming.
- Storage: in solvent -80°C for up to 6 months; sealed -20°C for up to 1 month.
- Supplied in small research pack sizes suitable for preclinical studies.
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Medchemexpress LLC Tivanisiran (siRNA) | 1848224-71-4 | 97.5% | 12068.30 (AS: 5294.6 + SS: 6125.7) | C361H447N141O262P36 | 5 MG
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Tivanisiran (SYL1001) is a double-stranded small interfering RNA (siRNA) designed to silence transient receptor potential vanilloid 1 (TRPV1) mRNA for research into dry eye disease. It is supplied as an oligonucleotide reagent intended for laboratory and preclinical gene-silencing studies.
- Silences TRPV1 mRNA to reduce ocular discomfort in dry eye models.
- Double-stranded siRNA sequence for targeted gene knockdown.
- High purity suitable for research applications (97.5%).
- Characterized molecular weight approximately 12,068 Da.
- Available in small pack sizes suitable for experiments (for example, 5 mg).
- Sequence information provided to support assay design and verification.
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