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Triterpenoids

Compounds with a carbon skeleton based on six isoprene units that are derived biosynthetically from the acyclic C30 hydrocarbon, squalene. They have relatively complex cyclic structures, most being either alcohols, aldehydes or carboxylic acids.
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Keyword Search:
16 – 30 of 198 results
16

Forskolin, (from Coleus forskohlii), MP Biomedicals™

CAS: 66575-29-9 Molecular Formula: C22H34O7 Molecular Weight (g/mol): 410.507 MDL Number: MFCD00082317 InChI Key: OHCQJHSOBUTRHG-KGGHGJDLSA-N Synonym: forskolin,colforsin,coleonol,colforsina,colforsine,colforsinum,boforsin,colforsine french,colforsinum latin,colforsina spanish PubChem CID: 47936 ChEBI: CHEBI:42471 IUPAC Name: [(3R,4aR,5S,6S,6aS,10S,10aR,10bS)-3-ethenyl-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-5-yl] acetate SMILES: CC(=O)OC1C(C2C(CCC(C2(C3(C1(OC(CC3=O)(C)C=C)C)O)C)O)(C)C)O

PubChem CID 47936
CAS 66575-29-9
Molecular Weight (g/mol) 410.507
ChEBI CHEBI:42471
MDL Number MFCD00082317
SMILES CC(=O)OC1C(C2C(CCC(C2(C3(C1(OC(CC3=O)(C)C=C)C)O)C)O)(C)C)O
Synonym forskolin,colforsin,coleonol,colforsina,colforsine,colforsinum,boforsin,colforsine french,colforsinum latin,colforsina spanish
IUPAC Name [(3R,4aR,5S,6S,6aS,10S,10aR,10bS)-3-ethenyl-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-5-yl] acetate
InChI Key OHCQJHSOBUTRHG-KGGHGJDLSA-N
Molecular Formula C22H34O7
18

Glycyrrhetic Acid 97.0+%, TCI America™

CAS: 471-53-4 Molecular Formula: C30H46O4 Molecular Weight (g/mol): 470.69 MDL Number: MFCD00003706,MFCD00066716 InChI Key: MPDGHEJMBKOTSU-YKLVYJNSSA-N Synonym: enoxolone,glycyrrhetinic acid,uralenic acid,glycyrrhetic acid,18-beta-glycyrrhetinic acid,glycyrrhetin,arthrodont,jintan,18beta-glycyrrhetinic acid,rhetinic acid PubChem CID: 10114 ChEBI: CHEBI:30853 IUPAC Name: (2S,4aS,6aS,6bR,8aR,10S,12aS,12bR,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-2-carboxylic acid SMILES: CC1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@]1(C)[C@@H]2C(=O)C=C2[C@@H]3C[C@](C)(CC[C@]3(C)CC[C@@]12C)C(O)=O

PubChem CID 10114
CAS 471-53-4
Molecular Weight (g/mol) 470.69
ChEBI CHEBI:30853
MDL Number MFCD00003706,MFCD00066716
SMILES CC1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@]1(C)[C@@H]2C(=O)C=C2[C@@H]3C[C@](C)(CC[C@]3(C)CC[C@@]12C)C(O)=O
Synonym enoxolone,glycyrrhetinic acid,uralenic acid,glycyrrhetic acid,18-beta-glycyrrhetinic acid,glycyrrhetin,arthrodont,jintan,18beta-glycyrrhetinic acid,rhetinic acid
IUPAC Name (2S,4aS,6aS,6bR,8aR,10S,12aS,12bR,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-13-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-2-carboxylic acid
InChI Key MPDGHEJMBKOTSU-YKLVYJNSSA-N
Molecular Formula C30H46O4
19

Forskolin 95.0+%, TCI America™

CAS: 66575-29-9 Molecular Formula: C22H34O7 Molecular Weight (g/mol): 410.507 MDL Number: MFCD00082317 InChI Key: OHCQJHSOBUTRHG-KGGHGJDLSA-N Synonym: forskolin,colforsin,coleonol,colforsina,colforsine,colforsinum,boforsin,colforsine french,colforsinum latin,colforsina spanish PubChem CID: 47936 ChEBI: CHEBI:42471 IUPAC Name: [(3R,4aR,5S,6S,6aS,10S,10aR,10bS)-3-ethenyl-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-5-yl] acetate SMILES: CC(=O)OC1C(C2C(CCC(C2(C3(C1(OC(CC3=O)(C)C=C)C)O)C)O)(C)C)O

PubChem CID 47936
CAS 66575-29-9
Molecular Weight (g/mol) 410.507
ChEBI CHEBI:42471
MDL Number MFCD00082317
SMILES CC(=O)OC1C(C2C(CCC(C2(C3(C1(OC(CC3=O)(C)C=C)C)O)C)O)(C)C)O
Synonym forskolin,colforsin,coleonol,colforsina,colforsine,colforsinum,boforsin,colforsine french,colforsinum latin,colforsina spanish
IUPAC Name [(3R,4aR,5S,6S,6aS,10S,10aR,10bS)-3-ethenyl-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-5-yl] acetate
InChI Key OHCQJHSOBUTRHG-KGGHGJDLSA-N
Molecular Formula C22H34O7
20

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

CAS: 915-05-9 Molecular Formula: C31H52O2 Molecular Weight (g/mol): 456.755 MDL Number: MFCD00083497 InChI Key: PBWOIPCULUXTNY-LBKBYZTLSA-N PubChem CID: 5354503 ChEBI: CHEBI:69433 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-yl] acetate SMILES: CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C

PubChem CID 5354503
CAS 915-05-9
Molecular Weight (g/mol) 456.755
ChEBI CHEBI:69433
MDL Number MFCD00083497
SMILES CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C
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-yl] acetate
InChI Key PBWOIPCULUXTNY-LBKBYZTLSA-N
Molecular Formula C31H52O2
21

Betulinic Acid 97.0+%, TCI America™

CAS: 472-15-1 Molecular Formula: C30H48O3 Molecular Weight (g/mol): 456.711 InChI Key: QGJZLNKBHJESQX-FZFNOLFKSA-N Synonym: betulinic acid,mairin,betulic acid,ccris 6748,3-hydroxylup-20 29-en-28-oic acid,3beta-hydroxy-20 29-lupaene-28-oic acid,3beta-hydroxy-lup-20 29-en-28-oic acid,lup-20 29-en-28-oic acid, 3-hydroxy-, 3beta,1r,3as,5ar,5br,7ar,9s,11ar,11br,13ar,13br-9-hydroxy-1-isopropenyl-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta a chrysene-3a-carboxylic acid,1r,3as,5ar,5br,7ar,9s,11ar,11br,13ar,13br-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta a chrysene-3a-carboxylic acid PubChem CID: 64971 ChEBI: CHEBI:3087 IUPAC Name: (1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid SMILES: CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O

PubChem CID 64971
CAS 472-15-1
Molecular Weight (g/mol) 456.711
ChEBI CHEBI:3087
SMILES CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O
Synonym betulinic acid,mairin,betulic acid,ccris 6748,3-hydroxylup-20 29-en-28-oic acid,3beta-hydroxy-20 29-lupaene-28-oic acid,3beta-hydroxy-lup-20 29-en-28-oic acid,lup-20 29-en-28-oic acid, 3-hydroxy-, 3beta,1r,3as,5ar,5br,7ar,9s,11ar,11br,13ar,13br-9-hydroxy-1-isopropenyl-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta a chrysene-3a-carboxylic acid,1r,3as,5ar,5br,7ar,9s,11ar,11br,13ar,13br-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta a chrysene-3a-carboxylic acid
IUPAC Name (1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid
InChI Key QGJZLNKBHJESQX-FZFNOLFKSA-N
Molecular Formula C30H48O3
22

Oleanolic Acid Hydrate 98.0+%, TCI America™

CAS: 508-02-1 Molecular Formula: C30H48O3 Molecular Weight (g/mol): 456.711 MDL Number: MFCD00064914 InChI Key: MIJYXULNPSFWEK-GTOFXWBISA-N Synonym: oleanolic acid,oleanic acid,caryophyllin,astrantiagenin c,giganteumgenin c,virgaureagenin b,3beta-hydroxyolean-12-en-28-oic acid,unii-6smk8r7tgj,ccris 6493,oleanolic_acid PubChem CID: 10494 ChEBI: CHEBI:37659 IUPAC Name: (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid SMILES: CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C

PubChem CID 10494
CAS 508-02-1
Molecular Weight (g/mol) 456.711
ChEBI CHEBI:37659
MDL Number MFCD00064914
SMILES CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C
Synonym oleanolic acid,oleanic acid,caryophyllin,astrantiagenin c,giganteumgenin c,virgaureagenin b,3beta-hydroxyolean-12-en-28-oic acid,unii-6smk8r7tgj,ccris 6493,oleanolic_acid
IUPAC Name (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
InChI Key MIJYXULNPSFWEK-GTOFXWBISA-N
Molecular Formula C30H48O3
23

Celastrol 98.0+%, TCI America™

CAS: 34157-83-0 Molecular Formula: C29H38O4 Molecular Weight (g/mol): 450.62 MDL Number: MFCD03424073 InChI Key: KQJSQWZMSAGSHN-JJWQIEBTSA-N Synonym: celastrol,tripterine,tripterin,2r,4as,6as,12br,14as,14br-10-hydroxy-2,4a,6a,9,12b,14a-hexamethyl-11-oxo-1,2,3,4,4a,5,6,6a,11,12b,13,14,14a,14b-tetradecahydropicene-2-carboxylic acid,triterpene,celastrol, celastrus scandens,unii-l8gg98663l,3-hydroxy-24-nor-2-oxo-1 10 ,3,5,7-friedelatetraen-29-oic acid,2r,4as,6ar,6as,14as,14br-10-hydroxy-2,4a,6a,6a,9,14a-hexamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylic acid,d:a-friedo-24-noroleana-1 10 ,3,5,7-tetraen-29-oic acid, 3-hydroxy-2-oxo-, 20alpha PubChem CID: 122724 ChEBI: CHEBI:63959 IUPAC Name: (2R,4aS,6aS,12bR,14aS,14bR)-10-hydroxy-2,4a,6a,9,12b,14a-hexamethyl-11-oxo-1,2,3,4,4a,5,6,6a,11,12b,13,14,14a,14b-tetradecahydropicene-2-carboxylic acid SMILES: CC1=C(O)C(=O)C=C2C1=CC=C1[C@@]2(C)CC[C@@]2(C)[C@@H]3C[C@@](C)(CC[C@]3(C)CC[C@]12C)C(O)=O

PubChem CID 122724
CAS 34157-83-0
Molecular Weight (g/mol) 450.62
ChEBI CHEBI:63959
MDL Number MFCD03424073
SMILES CC1=C(O)C(=O)C=C2C1=CC=C1[C@@]2(C)CC[C@@]2(C)[C@@H]3C[C@@](C)(CC[C@]3(C)CC[C@]12C)C(O)=O
Synonym celastrol,tripterine,tripterin,2r,4as,6as,12br,14as,14br-10-hydroxy-2,4a,6a,9,12b,14a-hexamethyl-11-oxo-1,2,3,4,4a,5,6,6a,11,12b,13,14,14a,14b-tetradecahydropicene-2-carboxylic acid,triterpene,celastrol, celastrus scandens,unii-l8gg98663l,3-hydroxy-24-nor-2-oxo-1 10 ,3,5,7-friedelatetraen-29-oic acid,2r,4as,6ar,6as,14as,14br-10-hydroxy-2,4a,6a,6a,9,14a-hexamethyl-11-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylic acid,d:a-friedo-24-noroleana-1 10 ,3,5,7-tetraen-29-oic acid, 3-hydroxy-2-oxo-, 20alpha
IUPAC Name (2R,4aS,6aS,12bR,14aS,14bR)-10-hydroxy-2,4a,6a,9,12b,14a-hexamethyl-11-oxo-1,2,3,4,4a,5,6,6a,11,12b,13,14,14a,14b-tetradecahydropicene-2-carboxylic acid
InChI Key KQJSQWZMSAGSHN-JJWQIEBTSA-N
Molecular Formula C29H38O4
24

Squalane, ≥99.0% (GC), Solstice

CAS: 111-01-3 Molecular Formula: C30H62 Molecular Weight (g/mol): 422.826 MDL Number: MFCD00008953 InChI Key: PRAKJMSDJKAYCZ-UHFFFAOYSA-N Synonym: squalane,perhydrosqualene,dodecahydrosqualene,cosbiol,vitabiosol,spinacane,robane,hexamethyltetracosane,tetracosane, 2,6,10,15,19,23-hexamethyl,hexamethyl tetracosane PubChem CID: 8089 IUPAC Name: 2,6,10,15,19,23-hexamethyltetracosane SMILES: CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C

PubChem CID 8089
CAS 111-01-3
Molecular Weight (g/mol) 422.826
MDL Number MFCD00008953
SMILES CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C
Synonym squalane,perhydrosqualene,dodecahydrosqualene,cosbiol,vitabiosol,spinacane,robane,hexamethyltetracosane,tetracosane, 2,6,10,15,19,23-hexamethyl,hexamethyl tetracosane
IUPAC Name 2,6,10,15,19,23-hexamethyltetracosane
InChI Key PRAKJMSDJKAYCZ-UHFFFAOYSA-N
Molecular Formula C30H62
25

Sigma Aldrich Squalane

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
Boiling Point 176°C (0.05 mmHg)
Percent Purity 96%
Linear Formula [(CH3)2 CH(CH2)3 CH(CH3)(CH2)3 CH(CH3)CH2CH2-]2
CAS 111-01-3
Molecular Weight (g/mol) 422.81
MDL Number MFCD00008953
Refractive Index n20/D 1.452 (literature)
Synonym 2,6,10,15,19,23-Hexamethyltetracosane; Cosbiol; Perhydrosqualene; Robane
RTECS Number XB6070000
Recommended Storage Room Temperature
Molecular Formula C30H62
Density 0.81 g/mL (at 25°C (literature))
Melting Point -38°C (lit.)
26

Medchemexpress LLC Lupeol | 545-47-1 | MFCD00017351 | 426.72 | 5 MG
SDP

Lupeol, also known as Clerodol, Monogynol B, or Fagarasterol, is an active pentacyclic triterpenoid. It exhibits anti-oxidant, anti-mutagenic, anti-tumor, and anti-inflammatory activities. This compound is a potent androgen receptor (AR) inhibitor, making it suitable for cancer research, particularly for prostate cancer of androgen-dependent phenotype (ADPC) and castration-resistant phenotype (CRPC).

  • Active pentacyclic triterpenoid
  • Potent androgen receptor (AR) inhibitor
  • Anti-oxidant activity
  • Anti-mutagenic activity
  • Anti-tumor activity
  • Anti-inflammatory activity
  • Used in cancer research, especially for prostate cancer

ENCOMPASS_PREFERRED
27

Apexbio Technology LLC Glycyrrhizic acid 1405-86-3 20mg

Glycyrrhizic acid (CAS 1405-86-3) is a triterpenoid saponin antagonist targeting high mobility group box 1 (HMGB1) and inhibitor of monoamine oxidase (MAO) as well as cytochrome P450 enzymes (CYP3A4 CYP2C9 CYP2C19) and 11 -hydroxysteroid dehydrogenase type 2 (11 -HSD2) It is designed to antagonize HMGB1-mediated pro-inflammatory responses and oxidative stress inhibit the enzymatic activity of MAO and 11 -HSD2 and modulate cytochrome P450-mediated metabolism Glycyrrhizic acid exerts its biological activity primarily through competitive inhibition of these enzymes It demonstrates MAO inhibition with an IC50 of approximately 0 16 M and competitively inhibits CYP3A4 (IC50 8 2 M) CYP2C9 ( 42 9 M) and CYP2C19 ( 40 3 M) Based on these pharmacological properties glycyrrhizic acid holds research potential in anti-inflammatory pathways enzyme inhibition and glucose metabolic modulation

ENCOMPASS_PREFERRED
28

Medchemexpress LLC OLEANOLIC ACID STAN 100 mg
SDP

OLEANOLIC ACID STAN 100MG

ENCOMPASS_PREFERRED
29

Medchemexpress LLC LIMONIN 500 mg
SDP

LIMONIN 500MG

ENCOMPASS_PREFERRED
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Apexbio Technology LLC LUPEOL-50MG

Lupeol (CAS No 545-47-1) is a pentacyclic triterpenoid found in various fruits vegetables and medicinal plants It is primarily researched in the fields of oncology and pharmacology due to its potential anticancer anti-inflammatory and antioxidant properties Lupeol exerts its effects by modulating key signaling pathways such as PI3K/Akt and NF- B which are critical in cellular proliferation apoptosis and inflammation Its in vitro activity often ranges from nanomolar to low micromolar concentrations showcasing its potency in different experimental setups Lupeol s applications extend to various cancer cell lines animal models of inflammation and drug screening processes to explore its therapeutic potential against tumors and inflammatory diseases Experimental concentrations typically depend on the specific research design allowing researchers to tailor studies for acute or chronic exposure assessments

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