Trigothysoid L

Inquiry

For Research Use Only.

Category

Diterpenoids

Cat.No.

NP1621

CAS

1501943-06-1

Product Name

Trigothysoid L

Structure

Product Details

Description

Trigothysoid L is a natural compound exhibiting commendable efficacy in studying autoimmune ailments, notably rheumatoid arthritand psoriasis. Its mechanism of action entails a substantial impediment to both T-cell activation and cytokine generation, thus inducing an immunosuppressive state.

Synonyms

7,9-Epoxy-3a,5-methano-3aH-cyclopenta[a][1,3]dioxolo[4,5-h][3]benzoxepin-3,6,11a,13(5H)-tetrol, decahydro-2,5,11-trimethyl-7a-(1-methylethenyl)-9-phenyl-, 3,6-diacetate 13-benzoate, (2S,3S,3aR,5R,6S,6aS,7R,7aS,9R,10aS,11R,11aR,11bS,13R)-

IUPAC Name

[(1R,2S,3S,4R,6R,7S,8S,10S,11R,12R,13S,15R,17S,19R)-3,7-diacetyloxy-11-hydroxy-4,8,12-trimethyl-15-phenyl-17-prop-1-en-2-yl-5,14,16,18-tetraoxahexacyclo[13.2.1.14,6.02,11.06,10.013,17]nonadecan-19-yl] benzoate

Molecular Weight

674.74

Molecular Formula

C38H42O11

Canonical SMILES

O=C(OC1C2(OC31C(OC(=O)C)C(C)CC3C4(O)C(C)C5OC6(OC(C4C2OC(=O)C)C5(O6)C(=C)C)C=7C=CC=CC7)C)C=8C=CC=CC8

InChI

InChI=1S/C38H42O11/c1-19(2)36-29-21(4)35(42)26-18-20(3)28(43-22(5)39)37(26)33(45-32(41)24-14-10-8-11-15-24)34(7,48-37)30(44-23(6)40)27(35)31(36)47-38(46-29,49-36)25-16-12-9-13-17-25/h8-17,20-21,26-31,33,42H,1,18H2,2-7H3/t20-,21+,26-,27-,28-,29-,30-,31+,33+,34+,35-,36-,37+,38+/m0/s1

InChIKey

WNPJCCBGGBXPSC-QEDJMQNKSA-N

Boiling Point

747.1±60.0°C (Predicted)

Purity

≥95%

Density

1.37±0.1 g/cm3 (Predicted)

Solubility

Soluble in Acetone, Chloroform, Dichloromethane, DMSO, Ethyl Acetate

Appearance

Powder

Storage

Store at -20°C

Color

Yellow

Form

Powder

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