Indoles and derivatives
- (1)
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- (1)
- (1)
- (54)
- (121)
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- (18)
- (2)
- (10)
- (1)
- (87)
- (1)
- (287)
- (2)
- (1)
- (6)
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- (1)
- (33)
- (1)
- (12)
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- (1)
- (1)
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- (21)
- (1)
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- (1)
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- (1)
- (1)
- (1)
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- (1)
- (1)
- (1)
- (1)
- (1)
- (7)
- (5)
- (1)
- (1)
- (1)
- (1)
- (2)
- (13)
- (2)
- (4)
- (7)
- (1)
- (10)
- (1)
- (6)
- (1)
- (11)
- (5)
- (4)
- (1)
- (5)
- (1)
- (1)
- (1)
- (1)
- (2)
- (11)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (4)
- (1)
- (1)
- (2)
- (2)
- (6)
- (2)
- (2)
- (4)
- (21)
- (16)
- (2)
- (2)
- (4)
- (2)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (7)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (13)
- (2)
- (1)
- (2)
- (1)
- (2)
- (1)
- (6)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (7)
- (3)
- (1)
- (1)
- (1)
- (2)
- (4)
- (8)
- (1)
- (1)
- (1)
- (7)
- (1)
- (1)
- (4)
- (5)
- (2)
- (2)
- (1)
- (1)
- (2)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (5)
- (4)
- (12)
- (1)
- (5)
- (2)
- (6)
- (1)
- (2)
- (2)
- (1)
- (1)
- (7)
- (2)
- (2)
- (1)
- (2)
- (1)
- (9)
- (7)
- (1)
- (3)
- (3)
- (1)
- (9)
- (2)
- (1)
- (2)
- (1)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (2)
- (7)
- (1)
- (4)
- (2)
- (2)
- (2)
- (3)
- (1)
- (1)
- (2)
- (4)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (5)
- (2)
- (1)
- (1)
- (2)
- (1)
- (4)
- (4)
- (2)
- (3)
- (5)
- (1)
- (2)
- (2)
- (1)
- (1)
- (6)
- (3)
- (8)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (3)
- (2)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (4)
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- (1)
- (1)
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- (1)
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- (3)
- (3)
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- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (4)
- (1)
- (2)
- (9)
- (7)
- (2)
- (1)
- (1)
- (1)
- (7)
- (2)
- (1)
- (2)
- (4)
- (4)
- (2)
- (2)
- (1)
- (4)
- (5)
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- (1)
- (2)
- (2)
- (1)
- (1)
- (8)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (17)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (4)
- (4)
- (5)
- (2)
- (1)
- (4)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (3)
- (1)
- (1)
- (4)
- (8)
- (2)
- (2)
- (6)
- (2)
- (2)
- (1)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (5)
- (4)
- (2)
- (2)
- (1)
- (2)
- (2)
- (1)
- (2)
- (3)
- (3)
- (2)
- (4)
- (4)
- (2)
- (2)
- (1)
- (1)
- (2)
- (5)
- (1)
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- (2)
- (1)
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- (2)
- (3)
- (22)
- (1)
- (7)
- (2)
- (4)
- (5)
- (2)
- (3)
- (26)
- (1)
- (177)
- (9)
- (17)
- (39)
- (70)
- (52)
- (9)
- (15)
- (2)
- (2)
- (10)
- (9)
- (1)
- (5)
- (2)
- (4)
- (19)
- (2)
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- (2)
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- (6)
- (5)
- (2)
- (3)
- (3)
- (1)
- (11)
- (3)
- (66)
- (23)
- (181)
- (2)
- (1)
- (126)
- (5)
- (43)
- (2)
- (2)
- (3)
- (494)
- (2)
- (5)
- (3)
- (5)
- (3)
- (4)
- (2)
- (2)
- (2)
- (31)
- (1)
- (66)
- (6)
- (3)
- (81)
- (2)
- (1)
- (1)
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Filtered Search Results
TARGETMOL CHEMICALS INC Carazolol 100MG
Also available in 25 mg, 50 mg and bulk. Please contact Fisher for quotes. Carazolol (Suacron) is a high-affinity antagonist/partial inverse agonist (also referred to as a beta blocker) of the beta-adrenergic receptor. Purity 99.08%
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Selleck Chemical LLC Carazolol
Carazolol is a non-specific -adrenergic receptor blocking agent and binds to receptors irreversibly
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eMolecules 102554-97-2 | 4-(4-Biphenylyl)-2-(4-pyridyl)thiazole | Oakwood Chemicals | MFCD12937797 | 314.410 | C20H14N2S | 97.000 | c1sc(nc1-c1ccc(cc1)-c1ccccc1)-c1ccncc1 | 1g | 480147611
4-(4-Biphenylyl)-2-(4-pyridyl)thiazole | Oakwood Chemicals | 102554-97-2 | MFCD12937797 | 314.410 | C20H14N2S | 97.000 | c1sc(nc1-c1ccc(cc1)-c1ccccc1)-c1ccncc1 | 1g | 480147611
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Medchemexpress LLC Indoline | 496-15-1 | MFCD00005705 | 99.9% | 119.17 g/mol | C8H9N | 1mL
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Indoline is a derivative of Indole (HY-W001132) Indoline can use as the basic structure for CD4 mimetic compounds (CD4mcs) which triggers conformational changes of the HIV-1 envelope glycoprotein (Env) in advance and causes viral inactivation Indoline binds to gp120 Indoline CD4mcs can inhibit HIV-1AD8 with an IC50 in the micromolar range[1]
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Medchemexpress LLC Indole-3-carboxylic acid | 771-50-6 | 161.16 | 10 G
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Indole-3-carboxylic acid is an orally active urinary indolic tryptophan metabolite. It acts as a mediator of priming against *Plectosphaerella cucumerina* and enhances the anti-colorectal cancer potency of Doxorubicin by inducing cell senescence. It can also be used in liver disease research.
- Orally active urinary indolic tryptophan metabolite.
- Mediates priming against *Plectosphaerella cucumerina*.
- Enhances anti-colorectal cancer potency by inducing cell senescence.
- Can be used in liver disease research.
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eMolecules 143612-79-7 | 3-(4-chlorobuty)indole-5-carbonitrile | MFCD09833261 | 25g
Ambeed | (4-Methoxypyridin-2-yl)methanamine | 100mg | 524984303 | A100929 | 194658-14-5 | MFCD11111886 | 138.170 | C7H10N2O
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eMolecules Building Block Tool<|a>
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Medchemexpress LLC INDOLE-2-CARBOXYLIC 10G
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INDOLE-2-CARBOXYLIC 10G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000770809 CARBOXYL DIAZIRINE A 250MG
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eMolecules TETRAHYDROFURAN-3-CARBOXYL 1MG
5000191687 TETRAHYDROFURAN-3-CARBOXYL 1MG
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eMolecules 3-OXOCYCLOBUTANE-1-CARBOXYL 5G
5000191637 3-OXOCYCLOBUTANE-1-CARBOXYL 5G
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Medchemexpress LLC INDOLE-2-CARBOXYLIC 50 mg
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INDOLE-2-CARBOXYLIC 50MG
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Medchemexpress LLC DISULFO-ICG CARBOXYL 5 mg
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DISULFO-ICG CARBOXYL 5MG
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Chemscene CHEMSCENE
5000579128 INDOLE-5-CARBOXYLIC ACID 9 10G
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Chemscene CHEMSCENE
5000579547 INDOLE-2-CARBOXYLIC ACID 10G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000743853 CLOPIDOGREL CARBOXYL 10MG
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