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nimbolide

Product Name
nimbolide
CAS No.
25990-37-8
Chemical Name
nimbolide
Synonyms
nimbolide;NSC 309909;Nimbolide (25 mg);Nimbolide, 10 mM in DMSO;Nimbolide, CyclinA and ERK1/2 inhibitor;(17R)-7α,15β:21,23-Diepoxy-6α-hydroxy-4,8-dimethyl-1-oxo-11-methoxycarbonyl-18,24-dinor-11,12-seco-5α-chola-2,13,20,22-tetrene-4α-carboxylic acid γ-lactone;methyl [(2aR,5aR,6S,6aR,8R,9aR,10aS,10bR,10cR)-8-furan-3-yl-2a,5a,6a,7-tetramethyl-2,5-dioxo-2a,5a,6,6a,8,9,9a,10a,10b,10c-decahydro-2H,5H-cyclopenta[d]naphtho[2,3-b:1,8-b''c'']difuran-6-yl]acetate;2H,5H-Cyclopenta[d']naphtho[1,8-bc:2,3-b']difuran-6-acetic acid, 8-(3-furanyl)-2a,5a,6,6a,8,9,9a,10a,10b,10c-decahydro-2a,5a,6a,7-tetramethyl-2,5-dioxo-, methyl ester, (2aR,5aR,6S,6aR,8R,9aR,10aS,10bR,10cR)-
CBNumber
CB11328652
Molecular Formula
C27H30O7
Formula Weight
466.52
MOL File
25990-37-8.mol
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nimbolide Property

Melting point:
>223°C (dec.)
Boiling point:
608.6±55.0 °C(Predicted)
Density 
1.32±0.1 g/cm3(Predicted)
storage temp. 
Hygroscopic, -20°C Freezer, Under Inert Atmosphere
solubility 
Chloroform, Ethyl Acetate
form 
powder
color 
Light Beige to Yellow
InChIKey
KMTFKEPRKBPCJW-UHFFFAOYSA-N
SMILES
C12C3(C)C=CC(=O)C1(C)C(CC(=O)OC)C1(C)C4C(C(C=C4C)C4=COC=C4)OC1C2OC3=O
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Safety

RTECS 
GY2370000
Toxicity
hamster,LD50,intraperitoneal,> 500mg/kg (500mg/kg),Toxicology Letters. Vol. 30, Pg. 159, 1986.
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SMB00586
Product name
Nimbolide
Purity
from Azadirachta indica, ≥98%
Packaging
5mg
Price
$354.9
Updated
2025/07/31
Cayman Chemical
Product number
19230
Product name
Nimbolide
Purity
≥97%
Packaging
5mg
Price
$251
Updated
2024/03/01
Cayman Chemical
Product number
19230
Product name
Nimbolide
Purity
≥97%
Packaging
25mg
Price
$1058
Updated
2024/03/01
Tocris
Product number
7289
Product name
Nimbolide
Purity
≥97%(HPLC)
Packaging
25
Price
$1029
Updated
2021/12/16
Usbiological
Product number
N2567-38
Product name
Nimbolide
Packaging
5mg
Price
$440
Updated
2021/12/16
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nimbolide Chemical Properties,Usage,Production

Chemical Properties

Light Beige Solid

Uses

Nimbolide, a natural triterpenoid present in the edible parts of the neem tree (Azadirachta indica), was found to be growth-inhibitory in human colon carcinoma HT-29 cells. Nimbolide treatment of cells at 2.5 - 10 μM resulted in moderate to very strong growth inhibition.

Biological Activity

Nimbolide exhibits anti-malarial, anti-bacterial, and anti-cancer activities. It has been shown to induce apoptosis in osteosarcoma cells and inhibits cell migration of these cells by modulating the expression of integrin αvβ5. In human renal carcinoma cells, nimbolide induced cell cycle arrest, DNA damage, and apoptosis.It has been shown to modulate autophagy and apoptosis in pancreatic cancer.

in vivo

Nimbolide (10 mg/kg, i.v., daily, 7 days) inhibits glioblastoma multiforme tumor growth in U87EGFRvⅢ xenografted mouse model[2].
Nimbolide (5 mg/kg, 20 mg/kg; i.p.; daily, 10 days), inhibits tumor growth in HCT-116-derived xenograft mouse, reduces the expression of proteins involved in invasion, metastasis, and angiogenesis (MMP-9, CXCR4, ICAM-1, and VEGF)[5].

Animal Model:HCT-116-derived xenograft mouse[5]
Dosage:5 mg/kg, 20 mg/kg
Administration:Intraperitoneal injection (i.p.), daily, 10 days
Result:Suppressed tumor growth in nude mice at a dose as low as 5 mg/kg.
Reduced tumor growth by almost 90% on day 10 at a dose as low as 20 mg/kg.
Didn’t affect the body weight of mice.

IC 50

NF-κB; CDK4; CDK6

storage

Store at -20°C

nimbolide Preparation Products And Raw materials

Raw materials

Preparation Products

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nimbolide Suppliers

Wuhan Acumen Bio-Technology Co.,ltd
Tel
027-027-16602739303 16602739303
Email
673003916@qq.com
Country
China
ProdList
2935
Advantage
58
Changsha Fuzhen Biotechnology Co.,LTD
Tel
0731-13823398 15111215862
Email
313359644@qq.com
Country
China
ProdList
4161
Advantage
58
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
ChemStrong Scientific Co.,Ltd
Tel
0755-0755-66853366 13670046396
Fax
0755-28363542
Email
sales@chem-strong.com
Country
China
ProdList
18333
Advantage
56
Finetech Industry Limited
Tel
027-87465837 19945049750
Fax
027-8777-2287
Email
sales@finetechnology-ind.com
Country
China
ProdList
9637
Advantage
58
Hangzhou J&H Chemical Co., Ltd.
Tel
0571-87396432
Fax
0571-87396431
Email
sales@jhechem.com
Country
China
ProdList
14912
Advantage
59
Watec Laboratories, Inc.
Tel
18602586511
Fax
0519-85267382
Email
info@wateclaboratories.com
Country
China
ProdList
170
Advantage
60
Wuhan ChemFaces Biochemical Co., Ltd.
Tel
18607101326 15172504745
Fax
+86-27-84254680
Email
aileen@chemfaces.com
Country
China
ProdList
6905
Advantage
55
Shanghai Synchem Pharma Co., ltd
Tel
21-619849051-1 18521059765
Email
synchempharma@aliyun.com
Country
China
ProdList
6468
Advantage
55

25990-37-8, nimbolideRelated Search:


  • nimbolide
  • (17R)-7α,15β:21,23-Diepoxy-6α-hydroxy-4,8-dimethyl-1-oxo-11-methoxycarbonyl-18,24-dinor-11,12-seco-5α-chola-2,13,20,22-tetrene-4α-carboxylic acid γ-lactone
  • NSC 309909
  • 2H,5H-Cyclopenta[d']naphtho[1,8-bc:2,3-b']difuran-6-acetic acid, 8-(3-furanyl)-2a,5a,6,6a,8,9,9a,10a,10b,10c-decahydro-2a,5a,6a,7-tetramethyl-2,5-dioxo-, methyl ester, (2aR,5aR,6S,6aR,8R,9aR,10aS,10bR,10cR)-
  • methyl [(2aR,5aR,6S,6aR,8R,9aR,10aS,10bR,10cR)-8-furan-3-yl-2a,5a,6a,7-tetramethyl-2,5-dioxo-2a,5a,6,6a,8,9,9a,10a,10b,10c-decahydro-2H,5H-cyclopenta[d]naphtho[2,3-b:1,8-b''c'']difuran-6-yl]acetate
  • Nimbolide (25 mg)
  • Nimbolide, CyclinA and ERK1/2 inhibitor
  • Nimbolide, 10 mM in DMSO
  • 25990-37-8
  • C27H30O72
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals