33289-85-9 Usage
Uses
Used in Pharmaceutical Industry:
Dipsacoside B is used as a cytotoxic agent for its ability to inhibit the growth and proliferation of cancer cells. It has demonstrated potential in targeting various types of cancer, including solid tumors, due to its natural cytotoxic properties.
Used in Drug Development:
Dipsacoside B is utilized as a key component in the development of novel anticancer drugs. Its cytotoxic nature allows researchers to explore its potential in creating new therapeutic options for cancer treatment, either as a standalone agent or in combination with other chemotherapeutic drugs.
Used in Cancer Research:
In the field of cancer research, Dipsacoside B serves as a valuable tool for studying the mechanisms of cancer cell growth and apoptosis. Its cytotoxic properties make it an important compound for investigating the underlying pathways involved in cancer progression and identifying potential targets for therapeutic intervention.
Used in Drug Delivery Systems:
Similar to gallotannin, Dipsacoside B can also be incorporated into drug delivery systems to enhance its bioavailability, delivery, and therapeutic outcomes. Researchers are exploring the use of various organic and metallic nanoparticles as carriers for Dipsacoside B, aiming to improve its overall effectiveness in cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 33289-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,8 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33289-85:
(7*3)+(6*3)+(5*2)+(4*8)+(3*9)+(2*8)+(1*5)=129
129 % 10 = 9
So 33289-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C53H86O22/c1-23-32(57)36(61)40(65)44(70-23)74-42-33(58)26(56)20-68-46(42)73-31-11-12-49(4)29(50(31,5)22-55)10-13-52(7)30(49)9-8-24-25-18-48(2,3)14-16-53(25,17-15-51(24,52)6)47(67)75-45-41(66)38(63)35(60)28(72-45)21-69-43-39(64)37(62)34(59)27(19-54)71-43/h8,23,25-46,54-66H,9-22H2,1-7H3/t23-,25?,26-,27+,28+,29?,30?,31-,32-,33-,34+,35+,36+,37-,38-,39+,40+,41+,42+,43+,44-,45-,46-,49-,50-,51+,52+,53-/m0/s1
33289-85-9Relevant academic research and scientific papers
Studies on the constituents of Hedera rhombea Bean. IV. On the hederagenin glycosides
Kizu,Hirabayashi,Suzuki,Tomimori
, p. 3473 - 3478 (2007/10/02)
On the basis of chemical and physicochemical evidence, the structures of two new hederagenin bisdesmosides, named Kizuta saponins K8 (X) and K11 (I), which were isolated from the stem and bark of Hedera rhombea Bean (Araliaceae), were established to be as follows: X, 3-O-α-L-arabinopyranosyl-hederagenin 28-O-α-L-rhamnopyranosyl-(1 →4)-6-O-acetyl-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester; I,3-O-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl-hederagenin 28-O-α-L-rhamnopyranosyl(1→4)-6-O-acetyl-β-D-glucopyranosyl-(1→6)-β-D -glucopyranosyl ester. A glucoside mixture (XIII) was considered to be a mixture of the β-D glucopyranosides of campesterol (trace), stigmasterol and β-sitosterol based on chemical and physicochemical evidence.
