accessibility menu, dialog, popup

UserName
Viewing profile as user:

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.

Filtered Search Results

Products from some of our suppliers do not display in filtered search results. Please clear all filters to see these products.

Narrow Results

Narrow Results

category

brands

  • (9)
  • (3)

special interests

  • (9)
Search Within Results
Keyword Search:
1 – 12 of 12 results
1

Medchemexpress LLC OP-5244 | 2381268-71-7 | 99.1% | C19H29ClN5O9P | 10MG
SDP

This compound is a potent, orally active CD73 (ecto-5'-nucleotidase, NT5E) inhibitor developed for cancer and immunology research. It blocks adenosine production to reverse immunosuppression and demonstrates low-nanomolar biochemical potency.

  • Potent CD73 inhibition with low-nanomolar biochemical potency.
  • Orally bioavailable in preclinical studies.
  • Reverses adenosine-mediated immunosuppression to enhance immune responses.
  • High reported purity suitable for research applications.
  • Available in small-quantity packages for screening and lead optimization.

ENCOMPASS_PREFERRED
2

Medchemexpress LLC BI-2545 | 2162961-71-7 | ≥98.0% | 527.4 g/mol | C23H19F6N5O3 | 100MG
SDP

BI-2545 is a research chemical probe that potently inhibits autotaxin (ATX) and lowers lysophosphatidic acid (LPA) levels in vivo. It is suitable for both in vitro and in vivo studies, shows selectivity in biochemical assays, and has documented whole-blood activity and favorable safety margins in preclinical profiling.

  • Potent ATX inhibition with human ATX IC50 ≈ 2.2 nM and rat ATX IC50 ≈ 3.4 nM.
  • Reduces LPA levels in vivo in animal studies.
  • Suitable for both in vitro and in vivo experimental use.
  • Demonstrated whole-blood activity (human ≈ 29 nM, rat ≈ 96 nM).
  • High chemical purity available (≥98.0%).
  • Molecular weight 527.4 g/mol; formula C23H19F6N5O3.

ENCOMPASS_PREFERRED
3

eMolecules​ Medchem Express / AEG3482 / 5mg / 673358654 / HY-107599 / / 63735-71-7 / MFCD02064987 / 280.320 / C10H8N4O2S2

Medchem Express / AEG3482 / 5mg / 673358654 / HY-107599 / / 63735-71-7 / MFCD02064987 / 280.320 / C10H8N4O2S2

ENCOMPASS_PREFERRED
4

eMolecules​ Medchem Express / CAY10526 / 5mg / 771358295 / HY-118119 / / 938069-71-7 / [null] / 311.150 / C12H7BrO3S

Medchem Express / CAY10526 / 5mg / 771358295 / HY-118119 / / 938069-71-7 / [null] / 311.150 / C12H7BrO3S

ENCOMPASS_PREFERRED
5

Medchemexpress LLC Trans-3-indoleacrylic acid | 29953-71-7 | MFCD00005633 | 99.4% | 187.19 g/mol | C11H9NO2 | 50 MG
SDP

Trans-3-indoleacrylic acid (CAS 29953-71-7) is a tryptophan metabolite used in biochemical research and reported to inhibit ferroptosis in cell-based studies. It is provided as a high-purity solid and as a ready-to-use DMSO solution for in vitro applications.

  • High purity suitable for biochemical and cell biology assays.
  • Available as a solid and as a 10 mM solution in DMSO for convenience.
  • Relevant for ferroptosis and metabolic pathway research.
  • Molecular weight and formula provided for analytical reference.
  • Supplied in small research-friendly packaging sizes.

ENCOMPASS_PREFERRED
6

Medchemexpress LLC Trans-3-indoleacrylic acid | 29953-71-7 | MFCD00005633 | 99.4% | 187.19 g/mol | C11H9NO2 | 100 MG
SDP

Trans-3-indoleacrylic acid is a tryptophan metabolite used in biochemical research. It modulates ferroptosis by inhibiting RSL3-induced ferroptosis via the AHR-ALDH1A3-FSP1-CoQ10 axis and is applied in studies of colorectal carcinogenesis and cellular metabolism.

  • High purity (99.4%).
  • Molecular weight 187.19 g/mol.
  • Chemical formula C11H9NO2.
  • Soluble in DMSO up to 250 mg/mL; ultrasonic recommended.
  • Stored as powder at -20°C for long-term stability.
  • Available in multiple small-scale quantities suitable for research.

ENCOMPASS_PREFERRED
7

eMolecules​ Medchem Express / BI-2545 / 5mg / 532149168 / HY-124772 / / 2162961-71-7 / [null] / 527.427 / C23H19F6N5O3

Medchem Express / BI-2545 / 5mg / 532149168 / HY-124772 / / 2162961-71-7 / [null] / 527.427 / C23H19F6N5O3

ENCOMPASS_PREFERRED
8

Medchemexpress LLC N-(7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)demethyltamoxifen | 1481401-71-1 | 99.8% | 10 MG
SDP

FLTX1 is a fluorescent tamoxifen derivative used to label intracellular tamoxifen-binding sites (estrogen receptors) in permeabilized and non-permeabilized cells. It retains antiestrogenic activity of tamoxifen in breast cancer cells while lacking estrogenic agonist effects on the uterus. Supplied as a high-purity research reagent for cellular imaging and receptor localization studies.

  • Fluorescent probe for estrogen receptor localization.
  • Retains antiestrogenic activity without uterine agonism.
  • High purity suitable for imaging and biochemical assays.
  • Soluble in DMSO; available as solid or solution formats.
  • Available in multiple packaging sizes, including 10 MG for small-scale studies.

ENCOMPASS_PREFERRED
9

Medchemexpress LLC 3,5-bis(trifluoromethyl)benzyl azabicyclo[3.1.0]hexane carboxylate | 2162961-71-7 | ≥98.0% | 527.4 | C23H19F6N5O3 | 25MG
SDP

BI-2545 is a small-molecule chemical probe developed for research that potently inhibits autotaxin (ATX) and is suitable for both in vitro and in vivo studies. It demonstrates single-digit nanomolar biochemical potency against ATX and has been shown to lower plasma lysophosphatidic acid (LPA) levels following oral dosing in rodents.

ENCOMPASS_PREFERRED
10

Medchemexpress LLC 6-phenylimidazo[2,1-b]thiadiazole-2-sulfonamide | 63735-71-7 | MFCD02064987 | 99.8% | 280.33 g·mol⁻1 | C10H8N4O2S2 | 5 MG
SDP

AEG3482 is a small-molecule JNK inhibitor used in research to probe apoptosis and stress-response signaling. It binds Hsp90, promotes HSF1-dependent induction of heat shock proteins such as Hsp70 and Hsp25, and shows antiapoptotic activity in cellular and in vivo models. Supplied as a solid for laboratory use, it is intended for research only.

ENCOMPASS_PREFERRED
11

Medchemexpress LLC Benzotriazole-5-carbonylamino methyl 3-azabicyclo[3.1.0]hexane-3-carboxylate | 2162961-71-7 | >98.0% | 527.4 g/mol | C23H19F6N5O3 | 50MG
SDP

BI-2545 is a potent autotaxin (ATX) inhibitor developed as a chemical probe for in vitro and in vivo research. It exhibits single-digit nanomolar potency against purified ATX and lowers plasma lysophosphatidic acid (LPA) levels in animal studies, with demonstrated oral activity in rats. The compound is provided as a solid and has reported chemical identifiers and physical properties suitable for laboratory use.

ENCOMPASS_PREFERRED
12

Medchemexpress LLC (Z)-4-hydroxy-N'-((2-oxonaphthalen-1(2H)-ylidene)methyl)benzohydrazide | 2250156-71-7 | 99.0% | 306.32 g/mol | C18H14N2O3 | 5 MG
SDP

MEISi-2 is a small-molecule, selective inhibitor of MEIS transcription factors developed for research into hematopoietic stem cell self-renewal, cardiac injury, bone marrow transplantation, and cancer. Supplied as a high-purity research reagent, it is intended for in vitro screening and mechanistic studies.

  • Selective MEIS transcription factor inhibition for target validation.
  • High purity suitable for biochemical and cell-based assays.
  • Small pack size ideal for screening and pilot experiments.
  • Molecular weight 306.32 g/mol and formula C18H14N2O3 for accurate dosing calculations.
  • Supplied with CAS number 2250156-71-7 for unambiguous identification.

ENCOMPASS_PREFERRED