Berbamine (dihydrochloride)

Base Information Edit

Chemical Name:Berbamine (dihydrochloride)
CAS No.:6078-17-7
Molecular Formula:C₃₇H₄₀N₂O₆*2ClH
Molecular Weight:681.656
Hs Code.:2933990090
European Community (EC) Number:207-523-5,623-510-0
UNII:K44OC6U989
ChEMBL ID:CHEMBL3142494
Metabolomics Workbench ID:140042
NCI Thesaurus Code:C162340
Wikidata:Q27896680
Wikipedia:Berbamine
Mol file:6078-17-7.mol

Synonyms:(+)-berbamine;16h-1,24:6,9-dietheno-11,15-metheno-2H-pyrido(2',3':17,18)(1,11)dioxacycloeicosino(2,3,4-ij)isoquinolin-12-ol, 3,4,4a,5,16a,17,18,19-octahydro-21,22,26-trimethoxy-4,17-dimethyl-, (4aS,16aR)-;16h-1,24:6,9-dietheno-11,15-metheno-2H-pyrido(2',3':17,18)(1,11)dioxacycloeicosino(2,3,4-ij)isoquinolin-12-ol, 3,4,4a,5,16a,17,18,19-octahydro-21,22,26-trimethoxy-4,17-dimethyl-, (4aS-(4aR*,16aS*))-;16H-1,24:6,9-dietheno-11,15-metheno-2H-pyrido(2',3':17,18)(1,11)dioxacycloeicosino(2,3,4-ij)isoquinolin-12-ol, 3,4,4a,5,16a,17,18,19-octahydro-21,22,26-trimethoxy-4,17-dimethyl-, hydrochloride (1:2), (4aS,16aR)-;16H-1,24:6,9-dietheno-11,15-metheno-2H-pyrido(2',3':17,18)(1,11)dioxacycloeicosino(2,3,4-ij)isoquinolin-12-ol, 3,4,4a,5,16a,17,18,19-octahydro-21,22,26-trimethoxy-4,17-dimethyl-, hydrochloride, hydrate (1:1:4), (4aS,16aR)-;6,6',7-trimethoxy-2,2'-dimethylberbaman-12-ol;berbaman-12-ol, 6,6',7-trimethoxy-2,2'-dimethyl-;berbaman-12-ol, 6,6',7-trimethoxy-2,2'-dimethyl-, dihydrochloride;berbamine;berbamine dihydrochloride;berbamine hydrochloride;berbamine hydrochloride tetrahydrate;berbamine monohydrochloride;berbamine, (+);berbamine, (1'beta)-isomer;berbamine, (1beta)-isomer;berbamine, monohydrochloride, tetrahydrate;D-berbamine;penduline;pycnamine

Suppliers and Price of Berbamine (dihydrochloride)

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(+)-BerbamineDihydrochloride
50mg
$ 45.00

Sigma-Aldrich
Berbamine dihydrochloride
1g
$ 130.00

Sigma-Aldrich
Berbamine dihydrochloride phyproof? Reference Substance
25 mg
$ 218.00

Matrix Scientific
Berbamine dihydrochloride 95+%
5g
$ 504.00

Matrix Scientific
Berbamine dihydrochloride 95+%
1g
$ 189.00

DC Chemicals
Berbamine dihydrochloride >98%,StandardReferencesGrade
20 mg
$ 280.00

ChemScene
Berbamine dihydrochloride 95.25%
200mg
$ 60.00

ChemScene
Berbamine dihydrochloride 95.25%
500mg
$ 96.00

Biosynth Carbosynth
Berbamine dihydrochloride
1 g
$ 75.00

Biosynth Carbosynth
Berbamine dihydrochloride
2 g
$ 200.00

Total 70 raw suppliers

Chemical Property of Berbamine (dihydrochloride) Edit

Chemical Property:

Melting Point:270 °C
Boiling Point:744.4 °C at 760 mmHg
Flash Point:404 °C
PSA：72.86000
LogP:7.53720
Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C
Solubility.:≥68 mg/mL in DMSO; ≥10.68 mg/mL in H2O; ≥4.57 mg/mL in EtOH
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:680.2419925
Heavy Atom Count:47
Complexity:963

Purity/Quality:

98%,99%, ^*data from raw suppliers

(+)-BerbamineDihydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 22-36/37/38
Safety Statements: 26-36

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC.Cl.Cl
Isomeric SMILES:CN1CCC2=CC(=C3C=C2[C@@H]1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C[C@@H]6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC.Cl.Cl
Uses Reactant for:Preparation of and anti-leukemia active berbamine derivatives (+)-Berbamine Dihydrochloride exerts anti-inflammatory effects through inhibition of NF-κB and MAPK signalling pathways.

Technology Process of Berbamine (dihydrochloride)

There total 1 articles about Berbamine (dihydrochloride) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: