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Alcohols and polyols

Organic compounds containing one or more hydroxyl functional groups bonded to a carbon atom; hydroxyls consist of an oxygen atom bonded to a hydrogen atom. Alcohols exist in chain, or as closed rings. Polyols contain two or more hydroxyl groups.
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1

3-Cyclohexyl-1-propanol 99.0+%, TCI America™

CAS: 1124-63-6 Molecular Formula: C9H18O Molecular Weight (g/mol): 142.242 MDL Number: MFCD00001528 InChI Key: CLYAQFSQLQTVNO-UHFFFAOYSA-N Synonym: cyclohexanepropanol,3-cyclohexyl-1-propanol,3-cyclohexylpropanol,unii-kjb3vo906f,kjb3vo906f,cyclohexylpropyl alcohol,3-hydroxypropylcyclohexane,3-cyclohexylpropyl alcohol,acmc-1c5ti PubChem CID: 70763 IUPAC Name: 3-cyclohexylpropan-1-ol SMILES: C1CCC(CC1)CCCO

PubChem CID 70763
CAS 1124-63-6
Molecular Weight (g/mol) 142.242
MDL Number MFCD00001528
SMILES C1CCC(CC1)CCCO
Synonym cyclohexanepropanol,3-cyclohexyl-1-propanol,3-cyclohexylpropanol,unii-kjb3vo906f,kjb3vo906f,cyclohexylpropyl alcohol,3-hydroxypropylcyclohexane,3-cyclohexylpropyl alcohol,acmc-1c5ti
IUPAC Name 3-cyclohexylpropan-1-ol
InChI Key CLYAQFSQLQTVNO-UHFFFAOYSA-N
Molecular Formula C9H18O
2

1,3-Propanediol 98.0+%, TCI America™

CAS: 504-63-2 Molecular Formula: C3H8O2 Molecular Weight (g/mol): 76.10 MDL Number: MFCD00002949 InChI Key: YPFDHNVEDLHUCE-UHFFFAOYSA-N Synonym: 1,3-propanediol,trimethylene glycol,1,3-dihydroxypropane,2-deoxyglycerol,1,3-propylene glycol,1,3-propylenediol,1,3-propandiol,2-hydroxymethyl ethanol,omega-propanediol,beta-propylene glycol PubChem CID: 10442 ChEBI: CHEBI:16109 IUPAC Name: propane-1,3-diol SMILES: OCCCO

PubChem CID 10442
CAS 504-63-2
Molecular Weight (g/mol) 76.10
ChEBI CHEBI:16109
MDL Number MFCD00002949
SMILES OCCCO
Synonym 1,3-propanediol,trimethylene glycol,1,3-dihydroxypropane,2-deoxyglycerol,1,3-propylene glycol,1,3-propylenediol,1,3-propandiol,2-hydroxymethyl ethanol,omega-propanediol,beta-propylene glycol
IUPAC Name propane-1,3-diol
InChI Key YPFDHNVEDLHUCE-UHFFFAOYSA-N
Molecular Formula C3H8O2
3

D-Pinitol 98.0+%, TCI America™

CAS: 10284-63-6 Molecular Formula: C7H14O6 Molecular Weight (g/mol): 194.18 MDL Number: MFCD00216659 InChI Key: DSCFFEYYQKSRSV-FEPQRWDDSA-N Synonym: d-pinitol,pinitol,3-o-methyl-d-chiro-inositol,d-+-pinitol,inzitol,pinit,+-pinitol,methylinositol,sennitol,d-ononitol PubChem CID: 164619 IUPAC Name: (1R,2S,4S,5S)-6-methoxycyclohexane-1,2,3,4,5-pentol SMILES: COC1[C@@H](O)[C@@H](O)C(O)[C@H](O)[C@H]1O

PubChem CID 164619
CAS 10284-63-6
Molecular Weight (g/mol) 194.18
MDL Number MFCD00216659
SMILES COC1[C@@H](O)[C@@H](O)C(O)[C@H](O)[C@H]1O
Synonym d-pinitol,pinitol,3-o-methyl-d-chiro-inositol,d-+-pinitol,inzitol,pinit,+-pinitol,methylinositol,sennitol,d-ononitol
IUPAC Name (1R,2S,4S,5S)-6-methoxycyclohexane-1,2,3,4,5-pentol
InChI Key DSCFFEYYQKSRSV-FEPQRWDDSA-N
Molecular Formula C7H14O6
4

Medchemexpress LLC Olprinone hydrochloride | 119615-63-3 | 99.9% | C14H11ClN4O | 50 MG
SDP

Olprinone Hydrochloride is a potent phosphodiesterase (PDE) 3 inhibitor, showing IC50s of 0.35 μM for PDE3. It is utilized in research for heart failure due to its positive inotropic and vasodilative effects, and also demonstrates anti-inflammatory activity.

  • Potent PDE3 inhibitor
  • Used in research for heart failure
  • Exhibits positive inotropic and vasodilative effects
  • Demonstrates anti-inflammatory activity
  • Modulates inflammation associated with myocardial ischemia-reperfusion injury
  • Reduces pro-inflammatory cytokines such as TNF-α and IL-1β
  • Decreases expression of adhesion molecules like ICAM-1 and P-Selectin
  • Inhibits apoptosis related to myocardial injury

ENCOMPASS_PREFERRED
5

Medchemexpress LLC Olprinone hydrochloride | 119615-63-3 | 99.9% | C14H11ClN4O | 25 MG
SDP

Olprinone Hydrochloride, also known as Loprinone Hydrochloride, is a potent phosphodiesterase (PDE) 3 inhibitor with an IC50 of 0.35 μM. It is utilized in research for heart failure due to its positive inotropic and vasodilative effects, and it also demonstrates anti-inflammatory activity.

  • Potent PDE3 inhibitor (IC50 of 0.35 μM)
  • Used in research for heart failure
  • Exhibits positive inotropic and vasodilative effects
  • Demonstrates anti-inflammatory activity
  • Modulates inflammation associated with myocardial ischemia-reperfusion injury in rats
  • Reduces histological evidence of myocardial injury
  • Decreases pro-inflammatory cytokines (TNF-α and IL-1β)
  • Reduces adhesion molecules (ICAM-1 and P-Selectin)
  • Decreases nitrotyrosine formation and NF-κB expression
  • Reduces PAR formation and apoptosis

ENCOMPASS_PREFERRED
6

eMolecules​ 8-oxa-1-azaspiro[4.5]decane | 51130-63-3 | MFCD14581266 | 1g

Pharmablock | 8-oxa-1-azaspiro[4.5]decane | 1g | 551132258 | PBN2011959 | | 51130-63-3 | MFCD14581266 | 141.214 | C8H15NO

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ENCOMPASS_PREFERRED
7

Medchemexpress LLC Olprinone hydrochloride | 119615-63-3 | MFCD01749474 | ≥98.0% | 286.72 g·mol⁻¹ | C14H11ClN4O | 5 MG
SDP

Olprinone hydrochloride is a research-grade phosphodiesterase 3 (PDE3) inhibitor provided as an analytical standard for pharmacological and biochemical studies, commonly used in investigations of cardiac inotropy and vasodilation. The material is characterized for laboratory use and supplied in small pack sizes for precise dosing in experimental workflows.

  • Research-grade analytical standard suitable for assay development and characterization.
  • Selective phosphodiesterase 3 (PDE3) inhibitory activity relevant to cardiac function studies.
  • Provided in small pack sizes for precise dosing and handling in the laboratory.
  • Molecular formula C14H11ClN4O and molecular weight 286.72 g·mol⁻¹ for reproducible calculations.
  • Available with high purity specifications to support reliable experimental results.

ENCOMPASS_PREFERRED
8

eMolecules​ Ambeed / trans-2-Aminocyclohexanol hydrochloride / 1g / 552736258 / A484581 / / 5456-63-3 / [null] / 303.270 / C12H28Cl2N2O2

Ambeed / trans-2-Aminocyclohexanol hydrochloride / 1g / 552736258 / A484581 / / 5456-63-3 / [null] / 303.270 / C12H28Cl2N2O2

ENCOMPASS_PREFERRED
9

Medchemexpress LLC Benzoic acid, 4-[4-[[(3R)-1-butyl-3-[(R)-cyclohexylhydroxymethyl]-2,5-dioxo-1,4,9-triazaspiro [5.5]undec-9-yl]methyl]phenoxy]-, hydrochloride (1:1) | 461023-63-2 | 99.9% | 614.17 | 1 ML
SDP

Aplaviroc hydrochloride, an SDP derivative, is a potent CCR5 antagonist. It exhibits strong activity against various HIV-1 strains, including wild-type and multidrug-resistant variants, by binding to CCR5 with high affinity and inhibiting gp120/CD4 binding. This compound has been shown to suppress R5 HIV-1 viremia in in vivo models.

  • Potent activity against three wild-type R5 HIV-1 strains (HIV-1Ba-L, HIV-1JRFL, and HIV-1MOKW).
  • Substantially more potent than previously published CCR5 inhibitors.
  • Suppresses infectivity and replication of two HIV-1MDR variants.
  • Binds to CCR5 with high affinity.
  • Potently blocks rgp120/sCD4 binding to CCR5.
  • Exerts potent anti-R5 human immunodeficiency virus type 1 effects in a novel AIDS mouse model.
  • Suppresses R5 HIV-1 viremia in hu-PBMC-NOG mice.

ENCOMPASS_PREFERRED
10

Medchemexpress LLC Benzoic acid, 4-[4-[[(3R)-1-butyl-3-[(R)-cyclohexylhydroxymethyl]-2,5-dioxo-1,4,9-triazaspiro [5.5]undec-9-yl]methyl]phenoxy]-, hydrochloride (1:1) | 461023-63-2 | 99.9% | 614.17 | 25 MG
SDP

Aplaviroc hydrochloride is a CCR5 antagonist derived from SDP, with IC50s ranging from 0.1-0.4 nM for HIV-1Ba-L, HIV-1JRFL, and HIV-1MOKW. It is intended for research use only.

  • Target: CCR5 antagonist
  • Potency: Potent activity against wild-type R5 HIV-1 strains with IC50 values of 0.1 to 0.4 nM
  • Mechanism: Suppresses infectivity and replication of HIV-1MDR variants at low concentrations (IC50 values of 0.4 to 0.6 nM)
  • Binding Affinity: Binds to CCR5 with high affinity (Kd value of 2.9±1.0 nM)
  • Inhibition: Potently blocks rgp120/sCD4 binding to CCR5 with an IC50 value of 2.7 nM
  • In Vivo Efficacy: Suppresses R5 HIV-1 viremia in hu-PBMC-NOG mice at a dosage of 60 mg/kg

ENCOMPASS_PREFERRED
11

Sigma Aldrich 1,3-Propanediol

MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

ENCOMPASS ENCOMPASS_PREFERRED
Boiling Point 214°C (760 mmHg)
Linear Formula HO(CH2)3 OH
Molecular Weight (g/mol) 76.09
Density 1.053 g/mL (at 25°C (literature))
Percent Purity 98%
CAS 504-63-2
MDL Number MFCD00002949
Refractive Index n20/D 1.440 (literature)
Synonym 1,3-Dihydroxypropane; Bio-PDO; PG; Trimethylene glycol
RTECS Number TY2010000
Recommended Storage Room Temperature
Molecular Formula C3H8O2
EINECS Number 207-997-3
Melting Point -27°C (lit.)
12

Medchemexpress LLC Cct241533 hydrochloride | 1431697-96-9 | 98.55% | 478.94 | 50 MG
SDP

CCT241533 hydrochloride is a potent and selective CHK2 inhibitor with an IC50 of 3 nM and a Ki of 1.16 nM. It exhibits minimal cross-reactivity against a panel of kinases at 1 μM. X-ray crystallography confirms its binding to CHK2 in the ATP pocket. The compound blocks CHK2 activity in human tumor cell lines in response to DNA damage, significantly enhancing the cytotoxicity of two structurally distinct PARP inhibitors. Clear induction of the pS516 CHK2 signal by PARP inhibitor alone is abolished by CCT241533. The cytotoxicity (GI50) in HT-29, HeLa, and MCF-7 cells is 1.7, 2.2, and 5.1 μM, respectively.

  • Potent and selective CHK2 inhibitor (IC50=3 nM)
  • 63-fold selectivity over CHK1 (IC50=190 nM)
  • Low hERG inhibition (IC50=22 μM)
  • Blocks CHK2 activity in human tumor cell lines in response to DNA damage
  • Enhances cytotoxicity of PARP inhibitors

ENCOMPASS_PREFERRED