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C24-propyl sterols and derivatives

Organic compounds that consist of sterols, a class of tetracyclic compounds with a cyclopentane perhydrophenanthrene nucleus, a hydroxyl group at position 3 of the A-ring, and a side chain located at carbon 17.
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1

Phytosterols, Practical Grade, MP Biomedicals™

CAS: 83-46-5 Molecular Formula: C29H50O Molecular Weight (g/mol): 414.718 InChI Key: KZJWDPNRJALLNS-VJSFXXLFSA-N Synonym: 22,23-dihydrostigmasterol,α-Dihydrofucosterol,24β-Ethylcholesterol,5-Stigmasten-3β-ol,22,23-dihydrostigmasterol,azuprostat,triastonal,cinchol,rhamnol,harzol PubChem CID: 222284 ChEBI: CHEBI:27693 IUPAC Name: (3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol SMILES: CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C

PubChem CID 222284
CAS 83-46-5
Molecular Weight (g/mol) 414.718
ChEBI CHEBI:27693
SMILES CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C
Synonym 22,23-dihydrostigmasterol,α-Dihydrofucosterol,24β-Ethylcholesterol,5-Stigmasten-3β-ol,22,23-dihydrostigmasterol,azuprostat,triastonal,cinchol,rhamnol,harzol
IUPAC Name (3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
InChI Key KZJWDPNRJALLNS-VJSFXXLFSA-N
Molecular Formula C29H50O
2

Beta-Sitosterol From Soybeans Practical MP Biomedicals

CAS: 83-46-5 Molecular Formula: C29H50O Molecular Weight (g/mol): 414.718 InChI Key: KZJWDPNRJALLNS-VJSFXXLFSA-N Synonym: beta-sitosterol,sitosterol,cupreol,quebrachol,22,23-dihydrostigmasterol,azuprostat,triastonal,cinchol,rhamnol,harzol PubChem CID: 222284 ChEBI: CHEBI:27693 IUPAC Name: (3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol SMILES: CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C

PubChem CID 222284
CAS 83-46-5
Molecular Weight (g/mol) 414.718
ChEBI CHEBI:27693
SMILES CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C
Synonym beta-sitosterol,sitosterol,cupreol,quebrachol,22,23-dihydrostigmasterol,azuprostat,triastonal,cinchol,rhamnol,harzol
IUPAC Name (3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
InChI Key KZJWDPNRJALLNS-VJSFXXLFSA-N
Molecular Formula C29H50O
3
Promotions Available

Stigmasterol, 95%, Thermo Scientific Chemicals

CAS: 83-48-7 Molecular Formula: C29H48O Molecular Weight (g/mol): 412.70 MDL Number: MFCD00003630 InChI Key: HCXVJBMSMIARIN-PHZDYDNGSA-N Synonym: stigmasterol,stigmasterin,beta-stigmasterol,stigmasta-5,22-dien-3beta-ol,24s-5,22-stigmastadien-3beta-ol,unii-99wuk5d0y8,stigmasta-5,22e-dien-3beta-ol,stigmasta-5,22-dien-3-beta-ol,3beta,22e-stigmasta-5,22-dien-3-ol,stigmasta-5,22-dien-3-ol, 3b,22e PubChem CID: 5280794 ChEBI: CHEBI:28824 IUPAC Name: (3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol SMILES: CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C

PubChem CID 5280794
CAS 83-48-7
Molecular Weight (g/mol) 412.70
ChEBI CHEBI:28824
MDL Number MFCD00003630
SMILES CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C
Synonym stigmasterol,stigmasterin,beta-stigmasterol,stigmasta-5,22-dien-3beta-ol,24s-5,22-stigmastadien-3beta-ol,unii-99wuk5d0y8,stigmasta-5,22e-dien-3beta-ol,stigmasta-5,22-dien-3-beta-ol,3beta,22e-stigmasta-5,22-dien-3-ol,stigmasta-5,22-dien-3-ol, 3b,22e
IUPAC Name (3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
InChI Key HCXVJBMSMIARIN-PHZDYDNGSA-N
Molecular Formula C29H48O
4

beta-Sitosterol (contains Campesterol) 40.0+%, TCI America™

CAS: 83-46-5 Molecular Formula: C29H50O Molecular Weight (g/mol): 414.718 MDL Number: MFCD00003631 InChI Key: KZJWDPNRJALLNS-VJSFXXLFSA-N Synonym: beta-sitosterol,sitosterol,cupreol,quebrachol,22,23-dihydrostigmasterol,azuprostat,triastonal,cinchol,rhamnol,harzol PubChem CID: 222284 ChEBI: CHEBI:27693 IUPAC Name: (3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol SMILES: CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C

PubChem CID 222284
CAS 83-46-5
Molecular Weight (g/mol) 414.718
ChEBI CHEBI:27693
MDL Number MFCD00003631
SMILES CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C
Synonym beta-sitosterol,sitosterol,cupreol,quebrachol,22,23-dihydrostigmasterol,azuprostat,triastonal,cinchol,rhamnol,harzol
IUPAC Name (3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
InChI Key KZJWDPNRJALLNS-VJSFXXLFSA-N
Molecular Formula C29H50O
5

Stigmasterol 90.0+%, TCI America™

CAS: 83-48-7 Molecular Formula: C29H48O Molecular Weight (g/mol): 412.70 MDL Number: MFCD00003630 InChI Key: HCXVJBMSMIARIN-PHZDYDNGSA-N Synonym: stigmasterol,stigmasterin,beta-stigmasterol,stigmasta-5,22-dien-3beta-ol,24s-5,22-stigmastadien-3beta-ol,unii-99wuk5d0y8,stigmasta-5,22e-dien-3beta-ol,stigmasta-5,22-dien-3-beta-ol,3beta,22e-stigmasta-5,22-dien-3-ol,stigmasta-5,22-dien-3-ol, 3b,22e PubChem CID: 5280794 ChEBI: CHEBI:28824 IUPAC Name: (1R,3aS,3bS,7S,9aR,9bS,11aR)-1-[(2R,3E,5S)-5-ethyl-6-methylhept-3-en-2-yl]-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-ol SMILES: CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C

PubChem CID 5280794
CAS 83-48-7
Molecular Weight (g/mol) 412.70
ChEBI CHEBI:28824
MDL Number MFCD00003630
SMILES CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C
Synonym stigmasterol,stigmasterin,beta-stigmasterol,stigmasta-5,22-dien-3beta-ol,24s-5,22-stigmastadien-3beta-ol,unii-99wuk5d0y8,stigmasta-5,22e-dien-3beta-ol,stigmasta-5,22-dien-3-beta-ol,3beta,22e-stigmasta-5,22-dien-3-ol,stigmasta-5,22-dien-3-ol, 3b,22e
IUPAC Name (1R,3aS,3bS,7S,9aR,9bS,11aR)-1-[(2R,3E,5S)-5-ethyl-6-methylhept-3-en-2-yl]-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-ol
InChI Key HCXVJBMSMIARIN-PHZDYDNGSA-N
Molecular Formula C29H48O
6

AVANTI POLAR LIPIDS INC SITOSTEROL SYN FRM PLANT 200MG
SDP

NC2587908 SITOSTEROL SYN FRM PLANT 200MG

ENCOMPASS
7

eMolecules​ 83-48-7 | STIGMASTEROL | AstaTech | MFCD00003630 | 412.702 | C29H48O | 95.000 | CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C | 100g | 449731639

STIGMASTEROL | AstaTech | 83-48-7 | MFCD00003630 | 412.702 | C29H48O | 95.000 | CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C | 100g | 449731639

ENCOMPASS_PREFERRED
8

eMolecules​ 83-48-7 | Stigmasterol | Broadpharm | MFCD00003630 | 412.702 | C29H48O | 0.000 | CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C | 1g | 809115460

Stigmasterol | Broadpharm | 83-48-7 | MFCD00003630 | 412.702 | C29H48O | 0.000 | CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C | 1g | 809115460

ENCOMPASS_PREFERRED
9

eMolecules​ 83-48-7 | STIGMASTEROL | AstaTech | MFCD00003630 | 412.702 | C29H48O | 95.000 | CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C | 5g | 449731637

STIGMASTEROL | AstaTech | 83-48-7 | MFCD00003630 | 412.702 | C29H48O | 95.000 | CC[C@H](\C=C\[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C | 5g | 449731637

ENCOMPASS_PREFERRED
10

Kyfora Bio STEMS (Stigmasterol Hemisuccinate) 1 GR

Stigmasterol hemisuccinate (STEMS) is a stigmasterol derivative that is responsive to changes in pH. Stigmasterol is a naturally occurring phytosterol lipid that is growing in the bioprocessing space for its ability to improve lipid nanoparticle (LNP)-based mRNA transfection efficiency. Conjugation to hemiscuccinate has been shown to improve the cellular uptake in acidic microenvironments, such as those around tumors.Key application(s): LNP, acid-delivery systems

ENCOMPASS
11

Medchemexpress LLC Stigmasta-5,22-dien-3-ol, (3β,22E)- | 83-48-7 | 98.5% | 412.69 | 1 G
SDP

Stigmasterol is an orally active, immunomodulatory agent with anti-inflammatory and neuroprotective effects. It can cross the blood-brain barrier. It activates AMPK, inhibiting NF-κB and NLRP3 signaling pathways. Stigmasterol reduces microglia-mediated neuroinflammation and alleviates cognitive impairment and Alzheimer's disease. It also regulates M1/M2 polarization of microglia through the TLR4/NF-κB pathway, reducing neuropathic pain.

  • Orally active immunomodulatory agent
  • Exhibits anti-inflammatory effects
  • Neuroprotective properties
  • Crosses the blood-brain barrier
  • Activates AMPK
  • Inhibits NF-κB and NLRP3 signaling pathways
  • Reduces microglia-mediated neuroinflammation
  • Alleviates cognitive impairment and Alzheimer's disease
  • Regulates M1/M2 polarization of microglia
  • Reduces neuropathic pain

ENCOMPASS_PREFERRED
12

Apexbio Technology LLC Sertraline HCl 79559-97-0 10mM (in 1mL DMSO)

Sertraline hydrochloride (CAS 79559-97-0) is a small molecule classified as a selective serotonin reuptake inhibitor (SSRI) It acts by inhibiting the reabsorption of serotonin (5-HT) into presynaptic neurons thereby increasing synaptic serotonin levels This modulation of serotonergic neurotransmission is widely utilized in neuropharmacological research to investigate the molecular and behavioral effects of altered serotonin signaling Sertraline HCl serves as a reference compound in studies of antidepressant mechanisms neurochemical pathway analysis and the modeling of affective disorders in preclinical systems

ENCOMPASS_PREFERRED
13

Medchemexpress LLC Sertraline hydrochloride | 79559-97-0 | >99.9% | 342.69 | 10 MG
SDP

Sertraline hydrochloride is an antidepressant classified as a selective serotonin reuptake inhibitor (SSRI). It is researched for various conditions such as major depressive disorder and obsessive-compulsive disorder.

  • Functions as a selective serotonin reuptake inhibitor (SSRI) antidepressant.
  • Researched for major depressive disorder and obsessive-compulsive disorder.
  • Inhibits high mobility group box 1 (HMGB1)- or tumor necrosis factor-α (TNF-α)-induced microglial activation.
  • Produces optimal anti-depression effects in chronic unpredictable mild stress (CUMS)-exposed mice.
  • Significantly reduces immobility time during forced swim test in female animals.
  • Does not alter spontaneous locomotor activity in all three genotypes regardless of sex difference.

ENCOMPASS_PREFERRED
14

Kyfora Bio Stigmasterol 1 GR

Stigmasterol is a naturally occurring phytosterol lipid that is growing in the bioprocessing space for its ability to improve lipid nanoparticle (LNP) uptake efficiency. LNPs are well known for facilitating the safe and effective delivery of mRNA to target cells, thus enabling therapeutic action. Cholesterol derivatives like stigmasterol offer two major benefits to LNP formulations: they can improve the stability of the LNP and they can increase the cellular uptake efficiency both in cell cultures and in vivo. Kyfora Bio's high purity, transfection grade stigmasterol can be used in conjunction with our other cationic lipid products to provide reliable performance for a variety of bioprocessing applications.Key application(s): LNP, mRNA vaccine

ENCOMPASS
15

Medchemexpress LLC Sertraline hydrochloride | 79559-97-0 | MFCD00895772 | 99.9% | 1 ML
SDP

Sertraline hydrochloride is an antidepressant classified as a selective serotonin reuptake inhibitor (SSRI). It is currently being researched for the treatment of various conditions, including major depressive disorder and obsessive-compulsive disorder.

  • Shows spermicidal activity against human spermatozoa.
  • Inhibits microglial activation and inflammatory mediator production.
  • Produces anti-depression effects in CUMS-exposed mice.
  • Reduced immobility time during forced swim test in female animals.

ENCOMPASS_PREFERRED