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3alpha-Akeboic acid is a naturally occurring triterpenoid compound found in plants such as Senecio vulgaris. It is known for its diverse biological activities, including anti-tumor, anti-inflammatory, and anti-diabetic properties. 3alpha-Akeboic acid's ability to inhibit cancer cell growth, induce apoptosis, and regulate inflammatory responses and blood sugar levels makes it a promising candidate for further research and potential therapeutic applications.

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  • 104777-61-9 Structure
  • Basic information

    1. Product Name: 3alpha-Akeboic acid
    2. Synonyms: 3alpha-Akeboic acid;3alpha-Akebonoic acid;3-Epiakebonoic acid;(3alpha)-3-Hydroxy-30-noroleana-12,20(29)-dien-28-oic acid
    3. CAS NO:104777-61-9
    4. Molecular Formula: C29H44O3
    5. Molecular Weight: 440.65786
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104777-61-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3alpha-Akeboic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3alpha-Akeboic acid(104777-61-9)
    11. EPA Substance Registry System: 3alpha-Akeboic acid(104777-61-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 104777-61-9(Hazardous Substances Data)

104777-61-9 Usage

Uses

Used in Pharmaceutical Industry:
3alpha-Akeboic acid is used as an anti-tumor agent for its ability to inhibit the growth of cancer cells and induce apoptosis, making it a potential candidate for cancer treatment.
Used in Anti-inflammatory Applications:
3alpha-Akeboic acid is used as an anti-inflammatory agent for its capacity to inhibit the production of inflammatory mediators, thereby reducing inflammation.
Used in Diabetes Treatment:
3alpha-Akeboic acid is used as a potential treatment for diabetes due to its demonstrated ability to regulate blood sugar levels and improve insulin sensitivity, suggesting its potential use in managing and treating diabetes.

Check Digit Verification of cas no

The CAS Registry Mumber 104777-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,7 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104777-61:
(8*1)+(7*0)+(6*4)+(5*7)+(4*7)+(3*7)+(2*6)+(1*1)=129
129 % 10 = 9
So 104777-61-9 is a valid CAS Registry Number.

104777-61-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4aS,6aS,6bR,8aR,10R,12aR,12bR,14bS)-10-Hydroxy-6a,6b,9,9,12a-pen tamethyl-2-methylene-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13 ,14b-octadecahydro-4a(2H)-picenecarboxylic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:104777-61-9 SDS

104777-61-9Downstream Products

104777-61-9Relevant articles and documents

Triterpenoid saponins and phenylethanoid glycosides from stem of Akebia trifoliata var. australis

Gao, Huimin,Wang, Zhimin

, p. 2697 - 2705 (2006)

A detailed phytochemical study on the 70% aqueous ethanol extract of stems of Akebia trifoliata (Thunb.) Koidz. var. australis (Diels) Rehd led to isolation of five compounds, together with 12 known triterpenoid saponins and three known phenylethanoid glycosides. The structures of the five compounds were elucidated on the basis of analysis of spectroscopic data and physicochemical properties as: 2α, 3β, 23-trihydroxy-30-norolean-12-en-28-oic acid β-d-glucopyranosyl ester (1), 2α, 3β, 23-trihydroxy-30-norolean-12-en-28-oic acid β-d-xylopyranosyl-(1 → 3)-O-α-d-rhamnopyranosyl-(1 → 4)-O-β-d-glucopyranosyl-(1 → 6)-O-β-d-glucopyranosyl ester (2), 2α, 3β, 23-trihydroxyurs-12-en-28-oic acid β-d-xylopyranosyl-(1 → 3)-O-α-l-rhamnopyranosyl-(1 → 4)-O-β-d-glucopyranosyl-(1 → 6)-O-β-d-glucopyranosyl ester (3), 3-β-[(β-d-glucopyranosyl-(1 → 3)-O-α-l-arabinopyranosyl)oxy]-23-hydroxy-30-norolean-12-en-28-oic acid α-l-rhamnopyranosyl-(1 → 4)-O-β-d-glucopyranosyl-(1 → 6)-O-β-d-glucopyranosyl ester (4) and 3-β-[(α-l-xylopyranosyl-(1 → 2)-O-α-l-arabinopyranosyl)oxy]-30-norolean-12-en-28-oic acid α-l-rhamnopyranosyl-(1 → 4)-O-β-d-glucopyranosyl-(1 → 6)-O-β-d-glucopyranosyl ester (5), named mutongsaponin A, B, C, D and E, respectively.

New 30-noroleanane triterpenoid saponins from Holboellia coriacea Diels

Ding, Wenbing,Li, Ye,Li, Guanhua,He, Hualiang,Li, Zhiwen,Li, Youzhi

, (2016)

Three new 30-noroleanane triterpenoid saponins, akebonoic acid 28-O-β-D-glucopyranosyl-(1″→6′)-β-D-glucopyranosyl ester (1), akebonoic acid 28-O-(6″-O-caffeoyl)-β-D-glucopyranosyl-(1″→6′)-β-D-glucopyranosyl ester (Holboelliside A, 2) and 3β,20α,24-trihydroxy-29-norolean-12-en-28-oic acid 3-O-(6′-O-caffeoyl)-β-D-glucopyranoside (Holboelliside B, 3) were isolated from the stems of Holboellia coriacea Diels, together with five known compounds, eupteleasaponin VIII (4), 3α-akebonoic acid (5), quinatic acid (6), 3β-hydroxy-30-norhederagenin (7) and quinatoside A (8). The structures of these compounds were determined on the basis of spectral and chemical evidence. Compounds 1-5 were evaluated for their inhibitory activity against three human tumors HepG2, HCT116 and SGC-7901 cell lines in vitro.

Bidesmoside triterpenoid glycosides from Stauntonia chinensis and relationship to anti-inflammation

Gao, Hao,Zhao, Feng,Chen, Guo-Dong,Chen, Shao-Dan,Yu, Yang,Yao, Zhi-Hong,Lau, Brad W.C.,Wang, Zhao,Li, Jin,Yao, Xin-Sheng

experimental part, p. 795 - 806 (2010/05/17)

Ten triterpenoid glycosides, yemuoside YM26-35 (1-9 and 12), were isolated from a traditional Chinese medicine known as "Ye Mu Gua" (Stauntonia chinensis DC.) along with two known ones, kalopanax saponin C (10) and sieboldianoside A (11). Their

TRITERPENOID SAPONINS OF Guaiacum officinale

Ahmad, Viqar Uddin,Bano, Shaheen,Fatima, Iqbal,Bano, Nasreen,Riccio, Raffaele,Minale, Luigi

, p. 31 - 34 (2007/10/02)

Three new nortriterpenoidal saponins, guaianins A, 1, A1, 2, and B, 3, have been isolated from the stem bark of Guaiacum officinale(Zygophyllaceae).The structure of these saponins have been established on the basis of spectral evidence as 3-O--30-norolea-12,20(29)-dien-28-oic acid, 3-O--30-norolea-12,20(29)-dien-28-oic acid and 3-O-(1-3)-α-L-arabinopyranosyl-30-norolea-12,20(29)-dien-28-O-β-D-glucopyranosyl ester, respectively.

Saponins from Leaves of Acanthopanax senticosus HARMS., Ciwujia; Structures of Ciwujianosides B, C1, C2, C3, C4, D1, D2 and E

Shao, Chun-Jie,Kasai, Ryoji,Xu, Jing-Da,Tanaka, Osamu

, p. 601 - 608 (2007/10/02)

Eleven triterpenoid saponins were isolated from the leaves of a Chinese folk medicine, Acanthopanax senticosus (RUPR. et MAXIM) HARMS.Of these compounds, three were identified as known saponins.The structures of eight new saponins named ciwujianosides B (1), C1, (2), C2 (3), C3 (4), C4 (5), D1 (6), D2 (7), and E (8) were elucidated to be as follows: (1), 3-O-α-rhamnopyranosyl-(1->2)-β-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (2), 3-O-α-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (3), 3-O-α-rhamnopyranosyl-(1->2)-α-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (4), 3-O-α-arabinopyranosyl oleanolic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl(1->6)-β-glucopyranosyl ester; (5), 3-O-α-rhamnopyranosyl-(1->2)-α-arabinopyranosyl oleanolic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (6), 3-O-α-arabinopyranosyl oleanolic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl(1->6)-β-glucopyranosyl ester; (7), 3-O-α-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-b-glucopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (8), 3-O-α-rhamnopyranosyl-(1->2)-α-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid.Keywords - Acanthopanax senticosus; Araliaceae; saponin; Chinese folk medicine; ciwujianoside; oleanolic acid glycoside; noroleanolic acid glycoside; 30-norolean-12,20(29)-dien-28-oic acid; ciwujia

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