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Tetrahydroisoquinolines

Organic heterocyclic compounds that consist of an isoquinoline ring with no double bonds; contains a benzene ring fused to a six-membered ring with one nitrogen atom and five carbon atoms.
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Search Within Results
Keyword Search:
226 – 240 of 290 results
226

eMolecules​ 372523-75-6 | Medchem Express | TCS-OX2-29 | 5mg | 446255494 | HY-100452 | MFCD26142103 | 397.519 | C23H31N3O3

Ambeed | 6-Chloro-5-methylpyridine-2-carbonitrile | 100mg | 600841941 | A504845 | 875293-89-3 | MFCD18257989 | 152.580 | C7H5ClN2

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227

eMolecules​ 53899-17-5 | 8-METHOXY-1,2,3,4-TETRAHYDROQUINOLINE | AstaTech | MFCD07800307 | 163.220 | C10H13NO | 95.000 | COc1cccc2CCCNc12 | 1g | 449746540

8-METHOXY-1,2,3,4-TETRAHYDROQUINOLINE | AstaTech | 53899-17-5 | MFCD07800307 | 163.220 | C10H13NO | 95.000 | COc1cccc2CCCNc12 | 1g | 449746540

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228

Medchemexpress LLC Nampt-IN-5 | 2380013-17-0 | 98.0% | C25H25N5O2 | 10MG
SDP

Nampt-IN-5 is a research-stage small molecule inhibitor of nicotinamide phosphoribosyltransferase (NAMPT) that demonstrates potent antiproliferative activity in cancer cell lines and has documented metabolic interaction with CYP3A4. The compound is characterized by a defined purity and recommended solvent/formulation guidance for both in vitro and in vivo studies, and is intended for research use only.

  • Potent nicotinamide phosphoribosyltransferase (NAMPT) inhibitor with sub-nanomolar cellular activity.
  • Demonstrated cellular IC50s of 0.7 nM (A2780) and 3.9 nM (COR-L23).
  • Inhibits CYP3A4, enabling metabolic interaction studies.
  • High purity (98.02%) suitable for research applications.
  • Soluble in DMSO and compatible with recommended in vivo formulations.
  • Stable as a powder at -20°C; follow solvent storage guidelines for solutions.

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229

eMolecules​ 2716849-16-8 | [1-Methyl-1,2,5,6-tetrahydropyridine-3-yl]boronic acid pinacol ester hydrochloride | J & W PharmLab LLC259.580 | C12H23BClNO2 | 96.000 | Cl.CN1CCC=C(C1)B1OC(C)(C)C(C)(C)O1 | 1g | 517670060

[1-Methyl-1,2,5,6-tetrahydropyridine-3-yl]boronic acid pinacol ester hydrochloride | J & W PharmLab LLC | 2716849-16-8259.580 | C12H23BClNO2 | 96.000 | Cl.CN1CCC=C(C1)B1OC(C)(C)C(C)(C)O1 | 1g | 517670060

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230

Medchemexpress LLC OLODANRIGAN 10MG
SDP

OLODANRIGAN 10mg CAS#1316755-16-4 C₃₂H₂₉NO₅ MW:507.58

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231

Medchemexpress LLC HY-15793 5mg Medchemexpress, NBI-98782 CAS:85081-18-1 Purity:>98%
SDP

Medchemexpress, HY-15793 5mg NBI-98782 CAS:85081-18-1 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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232

eMolecules​ 6024-85-7 | Medchem Express | Tetrahydropalmatine (hydrochloride) | 10mg | 602878490 | HY-N0300A | MFCD00156231 | 391.89 | C21H26ClNO4

Medchem Express | Tetrahydropalmatine (hydrochloride) | 10mg | 602878490 | HY-N0300A | 6024-85-7 | MFCD00156231 | 391.890 | C21H26ClNO4

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233

eMolecules​ (S)-2-CBZ-1,2,3,4-TETRAHYDROISOQUINOLINE-1-CARBOXYLIC ACID | 151004-90-9 | MFCD28404665 | 1g

AstaTech | (S)-2-CBZ-1,2,3,4-TETRAHYDROISOQUINOLINE-1-CARBOXYLIC ACID | 1g | 273166134 | 66325 | 95.000 | 151004-90-9 | MFCD28404665 | 311.337 | C18H17NO4

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234

Medchemexpress LLC Ecteinascidin 770 | 114899-80-8 | 99.8% | 770.85 g/mol | C40H42N4O10S | 10 MG
SDP

Ecteinascidin 770 is a 1,2,3,4-tetrahydroisoquinoline alkaloid natural product used in preclinical cancer research for its potent cytotoxic and apoptosis-inducing activities. It is typically handled as a solid and prepared in solvent for in vitro assays, showing low-nanomolar inhibitory potency across several human tumor cell lines.

  • Induces apoptosis in tumor cell lines.
  • Exhibits low-nanomolar potency (reported IC50 values in multiple lines).
  • Molecular formula C40H42N4O10S and molecular weight ~770.85 g/mol.
  • Soluble in DMSO for biological testing.
  • Supplied as a small solid vial suitable for research use.

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235

eMolecules​ Berbamine dihydrochloride | 6078-17-7 | MFCD11982910 | 1g

Matrix Scientific | Berbamine dihydrochloride | 1g | 490660386 | 99125 | 95.000 | 6078-17-7 | MFCD11982910 | 681.650 | C37H42Cl2N2O6

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236

Medchemexpress LLC Ecteinascidin 770 | 114899-80-8 | 99.8% | 770.85 | C40H42N4O10S | 50 MG
SDP

Ecteinascidin 770 is a tetrahydroisoquinoline alkaloid with potent cytotoxic and anticancer activity. It shows low-nanomolar IC50 values across multiple human cancer cell lines and is intended for preclinical in vitro research. The compound is provided as a high-purity solid or as a DMSO solution and is documented with CAS 114899-80-8, formula C40H42N4O10S, and molecular weight 770.85.

  • High purity (≈99.8%).
  • Potent cytotoxic activity with low-nanomolar IC50 in multiple human cancer cell lines.
  • Suitable for in vitro and preclinical research applications.
  • Available in mg-scale quantities and as DMSO solutions.
  • Characterized by CAS 114899-80-8, formula C40H42N4O10S, molecular weight 770.85.

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237

eMolecules​ 103893-45-4 | 5-hydroxy-2-(((tetrahydro-2H-pyran-2-yl)oxy)methyl)-4H-pyran-4-one | 250mg

Ambeed | 4-methoxy-3-(methoxycarbonyl)phenylboronic acid | 100mg | 600845513 | A678135 | 1071958-96-7 | MFCD23380361 | 209.990 | C9H11BO5

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238

Medchemexpress LLC HY-U00448 5mg Medchemexpress, ADDA 5 hydrochloride CAS:473268-46-1 Purity:>98%
SDP

Medchemexpress, HY-U00448 5mg ADDA 5 hydrochloride CAS:473268-46-1 ADDA 5 hydrochloride is a partial non-competitive inhibitor of cytochrome c oxidase (CcO) , with IC 50 s of 18.93 μM and 31.82 μM for purified CcO from human glioma and bovine heart, 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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239

eMolecules​ 486427-17-2 | Medchem Express | CIQ | 5mg | 446269330 | HY-18699 | MFCD04411904 | 467.95 | C26H26ClNO5

Medchem Express | c(phg-isoDGR-(NMe)k) (TFA) | 1mg | 495799750 | HY-111413A | | 717.704 | C29H42F3N9O9

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240

Medchemexpress LLC Nampt-IN-3 | 2121591-52-2 | 99.0% | 503.55 | 100 MG
SDP

Nampt-IN-3 (Compound 35) simultaneously inhibits nicotinamide phosphoribosyltransferase (NAMPT) and HDAC with IC50s of 31 nM and 55 nM, respectively. It effectively induces cell apoptosis and autophagy, leading to cell death.

  • Inhibits nicotinamide phosphoribosyltransferase (NAMPT) and HDAC with IC50s of 31 nM and 55 nM.
  • Effectively induces cell apoptosis and autophagy.
  • Leads to cell death.
  • Demonstrates cytotoxicity in human HCT116 cells with an IC50 of 2.4 μM.
  • Demonstrates cytotoxicity in human HepG2 cells with an IC50 of 4.5 μM.
  • Demonstrates cytotoxicity in human MDA-MB-231 cells with an IC50 of 10 μM.

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