Alcohols and polyols
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- (30)
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- (102)
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- (13)
- (14)
- (1)
- (2)
- (1)
- (26)
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- (1)
- (6)
- (1)
- (462)
- (9)
- (46)
- (11)
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- (1)
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- (145)
- (114)
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- (1)
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- (1)
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- (1)
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- (2)
- (2)
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- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
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- (2)
- (5)
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- (17)
- (15)
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- (2)
- (5)
- (4)
- (33)
- (4)
- (2)
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- (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)
- (4)
- (2)
- (1)
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- (3)
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- (24)
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- (5)
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- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (7)
- (4)
- (1)
- (1)
- (3)
- (6)
- (11)
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- (3)
- (1)
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- (14)
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- (2)
- (1)
- (3)
- (2)
- (10)
- (1)
- (2)
- (4)
- (4)
- (3)
- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (5)
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- (1)
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- (9)
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- (2)
- (12)
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- (1)
- (1)
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- (1)
- (1)
- (1)
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- (1)
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- (1)
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- (82)
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- (1)
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- (1)
- (81)
- (3)
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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000427589 URSOLIC ACID 100MG
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eMolecules EMOLECULES INC
5000492696 CIS-1 3-CYCLOHEXANEDIOL 1G
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eMolecules EMOLECULES INC
5000493241 CYCLOHEXANOL 100G
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Entegris Inc LITHOCHOLIC ACID-3-SULFATE 1MG
Lithocholic Acid-3-Sulfate Sodium Salt | Purity: 98% | 1mg
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Avanti Polar Lipids URSOCHOLIC ACID 5MG
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Ursocholic acid 5mg
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Selleck Chemical LLC METHYLPREDNISOLONE 50MG
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NC3706764 METHYLPREDNISOLONE 50MG
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A2B CHEM LLC
NC3970272 1R 2S-2-METHYLCYCLOHEXANOL
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eMolecules Medchem Express / Ginsenoside Rg1 / 5mg / 446274535 / HY-N0045 / / 22427-39-0 / MFCD00210293 / 801.024 / C42H72O14
Medchem Express / Ginsenoside Rg1 / 5mg / 446274535 / HY-N0045 / / 22427-39-0 / MFCD00210293 / 801.024 / C42H72O14
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Medchemexpress LLC JBI-589 | 2308504-22-3 | C29H28FN5O | 1 MG
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JBI-589 is a non-covalent, orally bioavailable, and isoform-selective inhibitor of PAD4. It reduces CXCR2 expression and blocks neutrophil chemotaxis, and has been shown to reduce primary tumor and metastases. This compound enhances the anti-tumor effect of checkpoint inhibitors, making it suitable for cancer research.
- Non-covalent and orally bioavailable
- Isoform-selective inhibitor of PAD4
- Reduces CXCR2 expression and blocks neutrophil chemotaxis
- Inhibits primary tumor growth and metastases
- Enhances anti-tumor effect of checkpoint inhibitors
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Medchemexpress LLC HY-101273 5mg Medchemexpress, BAR502 CAS:1612191-86-2 Purity:>98%
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Medchemexpress, HY-101273 5mg BAR502 CAS:1612191-86-2 BAR502 is a dual FXR and GPBAR1 agonist with IC 50 values of 2 μM and 0.4 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.
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Medchemexpress LLC Deprodone propionate | 20424-00-4 | 400.51 | 100 MG
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Deprodone propionate is a corticosteroid obtained by esterifying the 17-position of the prednisolone skeleton with propionic acid and deoxidating its 21-position. It is intended for research use only. Not for sale to patients. Deprodone propionate can exhibit its effects to the maximum extent and over a prolonged period of time, does not cause skin irritation, and is physicochemically stable. It can be maintained in a stably suspended state due to the thickening action of the suspending agent.
- Effective ingredient with prolonged action
- Does not cause skin irritation
- Physicochemically stable
- Maintained in a stably suspended state
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Medchemexpress LLC Ansofaxine hydrochloride | 916918-84-8 | 417.97 | 50 MG
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Ansofaxine hydrochloride is a triple reuptake inhibitor that inhibits serotonin, dopamine, and norepinephrine reuptake. In vivo studies show it rapidly penetrates the rat striatum, converts into desvenlafaxine, and increases 5-HT, dopamine, and norepinephrine levels, ultimately reducing immobility time.
- Inhibits serotonin, dopamine, and norepinephrine reuptake
- Rapidly penetrates rat striatum
- Increases 5-HT, dopamine, and norepinephrine levels
- Reduces immobility time
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Medchemexpress LLC Notoginsenoside Fc | 88122-52-5 | 5 MG
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Notoginsenoside Fc is a protopanaxadiol- (PPD-) type saponin isolated from the leaves of Panax notoginseng. It effectively counteracts platelet aggregation and can accelerate reendothelialization following vascular injury in diabetic rats by promoting autophagy.
- Effectively counteracts platelet aggregation
- Accelerates reendothelialization following vascular injury in diabetic rats by promoting autophagy
- Markedly upregulates the expression of LC3B and Beclin 1, and downregulates that of p62 in RAOECs (in vitro)
- Alleviates excessive neointimal formation following carotid artery injury in diabetic Sprague-Dawley rats (in vivo)
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eMolecules ChemScene / 222-Trifluoro-1-(pyridin-3-yl)ethanone / 100mg / 536796049 / CS-0063929 / 0.000 / 33284-21-8 / MFCD00799596 / 175.110 / C7H4F3NO
ChemScene / 222-Trifluoro-1-(pyridin-3-yl)ethanone / 100mg / 536796049 / CS-0063929 / 0.000 / 33284-21-8 / MFCD00799596 / 175.110 / C7H4F3NO
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Medchemexpress LLC Abiraterone decanoate | 2486052-18-8 | 99.7% | C34H49NO2 | 10MG
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Abiraterone decanoate is the decanoate ester prodrug of abiraterone designed to provide controlled release and prolonged CYP17 inhibition when formulated for intramuscular delivery. Supplied as a high-purity solid for research and formulation studies; consult the datasheet for purity, storage, and handling details.
- Provides controlled release of abiraterone for long-acting CYP17 inhibition.
- High purity suitable for research use (reported 99.69%).
- Solid (powder) physical form for formulation and preclinical studies.
- Documented storage: powder stable at -20°C for extended storage; solvent stability conditions provided in datasheet.
- Intended for use in preclinical and formulation research investigating long-acting androgen biosynthesis inhibition.
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