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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 |
MP Biomedicals, Inc 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 |
MP Biomedicals, Inc 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 |
Stigmasterol 90.0+%, TCI America™
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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 |
beta-Sitosterol (contains Campesterol) 40.0+%, TCI America™
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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 |
Sigma Aldrich Fine Chemicals Biosciences beta-Sitosterol >=70% | 83-46-5 | MFCD00003631 | 100G
beta-Sitosterol >=70% | Purity: >=70% | Mol Wt: 414.71 | 83-46-5 | MFCD00003631 | 100G

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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

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Sertraline HCl 79559-97-0 10mg
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

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Indofine Chemical STIGMASTEROL, Lipid Research, 83-48-7, 98+%, 1 gm
STIGMASTEROL, Lipid Research, 83-48-7, 98+%, 1 gm

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Sigma Aldrich Fine Chemicals Biosciences Stigmasterol ~95% | 83-48-7 | MFCD00003630 | 10G
Stigmasterol ~95% | Purity: ~95% | Mol Wt: 412.69 | 83-48-7 | MFCD00003630 | 10G

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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

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Cayman Chemical StIgmasterol 10g
Differs from BB-22 structurally by having the hydroxyquinoline group attached at the four carbon instead of through the eight position of the ring intended for forensic and research applications

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Chem-Impex International, Inc. b-Sitosterol | MFCD00003631 | 100G
b-Sitosterol, MFCD00003631, 100G

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Med Vet International Sertaline Hcl Tablets (Zoloft), 100mg, 30ct
Sertaline is a generic version of Zoloft. It is classified as an SRRI antidepressant that affects chemicals in the brain that may be unbalanced.

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AdipoGen Stigmasterol (10 g)
Chemical. CAS: 83-48-7. Formula: C29H48O. MW: 412.69. Stigmasterol is a phytosterol with chemical structure similar to cholesterol and anti-hypercholestrolemic activity. It exhibits anticancer, anti-inflammatory, antioxidant, antidiabetic, neuroprotective and immune-modulating properties. Stigmasterol exhibits antitumor effects in cancer cells mediated via inhibition of cell migration, cell cycle arrest, apoptosis/autophagy induction and angiogenesis inhibition. Stigmasterol is a potent in vitro antagonist of FXR (farnesoid X receptor), a DNA polymerase beta inhibitor and targets the GLUT4 glucose transporter. It has anti-osteoarthritic effects, by decreasing the expression of matrix metalloproteinases. Stigmasterol shows acetylcholinesterase inhibitory activity and also enriched glutamatergic synapses in cultures of brain neurons.

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