Ginsenoside Rb1 information

Ginsenoside Rb₁
Names
	IUPAC name 20-[β-D-Glucopyranosyl-(1→6)-β-D-glucopyranosyloxy]-12β-hydroxydammar-24-en-3β-yl β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside
	Systematic IUPAC name (12S,13R,14S,15S,16R,32R,33R,34S,35S,36R,51S,53aR,53bR,55aR,57S,59aR,59bR,511R,511aR,6S,82S,83R,84S,85S,86R,112R,113R,114S,115R,116R)-16,36,116-Tris(hydroxymethyl)-53a,53b,56,56,59a,6-hexamethyl-6-(4-methylpent-3-en-1-yl)hexadecahydro-51H-2,4,7,10-tetraoxa-1,11(2),3(3,2),8(2,6)-tetrakis(oxana)-5(7,1)-cyclopenta[a]phenanthrenaundecaphane-13,14,15,34,35,511,83,84,85,113,114,115-dodecol
	Other names Ginsenoside-Rb1; GRb 1; GSRb1; Panax saponin E; Panaxsaponin E; Panaxoside Rb1; Pseudoginsenoside D; Gynosaponin C; Gypenoside III; Sanchinoside E1; Sanchinoside R1; Sanchinoside Rb1; Arasaponin E1; Notoginsenoside Rb1;
Identifiers
CAS Number	41753-43-9;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:CHEBI:67989;
ChemSpider	8073937;
DrugBank	DB06749;
ECHA InfoCard	100.050.466
EC Number	255-532-8;
KEGG	C20713;
PubChem CID	9898279;
UNII	7413S0WMH6;
CompTox Dashboard (EPA)	DTXSID401316929 ;
	InChI InChI=1S/C54H92O23/c1-23(2)10-9-14-54(8,77-48-44(69)40(65)37(62)29(74-48)22-70-46-42(67)38(63)34(59)26(19-55)71-46)24-11-16-53(7)33(24)25(58)18-31-51(5)15-13-32(50(3,4)30(51)12-17-52(31,53)6)75-49-45(41(66)36(61)28(21-57)73-49)76-47-43(68)39(64)35(60)27(20-56)72-47/h10,24-49,55-69H,9,11-22H2,1-8H3/t24-,25+,26+,27+,28+,29+,30-,31+,32-,33-,34+,35+,36+,37+,38-,39-,40-,41-,42+,43+,44+,45+,46+,47-,48-,49-,51-,52+,53+,54-/m0/s1 Key: GZYPWOGIYAIIPV-JBDTYSNRSA-N;
	SMILES CC(=CCC[C@@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)C)O)C)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO)O)O)O)O)O)O)C;
Properties
Chemical formula	C54H92O23
Molar mass	1109.307 g·mol−1
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H302, H312, H332
Precautionary statements	P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Ginsenoside Rb₁ (or Ginsenoside Rb1 or GRb₁ or GRb1) is a chemical compound belonging to the ginsenoside family.

Like other ginsenosides, it is found in the plant genus Panax (ginseng), and has a variety of potential health effects including anticarcinogenic, immunomodulatory, anti‐inflammatory, antiallergic, antiatherosclerotic, antihypertensive, and antidiabetic effects as well as antistress activity and effects on the central nervous system.^[3]

^ PubChem. "Ginsenoside rb1 - Depositor-Supplied Synonyms". pubchem.ncbi.nlm.nih.gov. Retrieved 2020-07-24.
^ "Common Chemistry - Substance Details - 41753-43-9". www.commonchemistry.org. Retrieved 2020-07-29.
^ Christensen, L. P. (2008). "Chapter 1 Ginsenosides: Chemistry, Biosynthesis, Analysis, and Potential Health Effects". Advances in Food and Nutrition Research. 55: 1–99. doi:10.1016/S1043-4526(08)00401-4. PMID 18772102.

[1] PubChem. "Ginsenoside rb1 - Depositor-Supplied Synonyms". pubchem.ncbi.nlm.nih.gov. Retrieved 2020-07-24.

[2] "Common Chemistry - Substance Details - 41753-43-9". www.commonchemistry.org. Retrieved 2020-07-29.

[3] Christensen, L. P. (2008). "Chapter 1 Ginsenosides: Chemistry, Biosynthesis, Analysis, and Potential Health Effects". Advances in Food and Nutrition Research. 55: 1–99. doi:10.1016/S1043-4526(08)00401-4. PMID 18772102.

Ginsenoside Rb1 information

and 6 Related for: Ginsenoside Rb1 information

Ginsenoside Rb1

Ginsenoside

Panax notoginseng

Acremonium strictum

Terrabacter ginsenosidimutans

American ginseng

Names

IUPAC name 20-[β-D-Glucopyranosyl-(1→6)-β-D-glucopyranosyloxy]-12β-hydroxydammar-24-en-3β-yl β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside
Systematic IUPAC name (1²S,1³R,1⁴S,1⁵S,1⁶R,3²R,3³R,3⁴S,3⁵S,3⁶R,5¹S,5^3aR,5^3bR,5^5aR,5⁷S,5^9aR,5^9bR,5¹¹R,5^11aR,6S,8²S,8³R,8⁴S,8⁵S,8⁶R,11²R,11³R,11⁴S,11⁵R,11⁶R)-1⁶,3⁶,11⁶-Tris(hydroxymethyl)-5^3a,5^3b,5⁶,5⁶,5^9a,6-hexamethyl-6-(4-methylpent-3-en-1-yl)hexadecahydro-5¹H-2,4,7,10-tetraoxa-1,11(2),3(3,2),8(2,6)-tetrakis(oxana)-5(7,1)-cyclopenta[a]phenanthrenaundecaphane-1³,1⁴,1⁵,3⁴,3⁵,5¹¹,8³,8⁴,8⁵,11³,11⁴,11⁵-dodecol
Other names Ginsenoside-Rb1 GRb 1 GSRb1 Panax saponin E Panaxsaponin E Panaxoside Rb1 Pseudoginsenoside D Gynosaponin C Gypenoside III Sanchinoside E1 Sanchinoside R1 Sanchinoside Rb1 Arasaponin E1 Notoginsenoside Rb1 ^[1]^[2]
Identifiers
CAS Number	41753-43-9
3D model (JSmol)	Interactive image
ChEBI	CHEBI:CHEBI:67989
ChemSpider	8073937
DrugBank	DB06749
ECHA InfoCard	100.050.466
EC Number	255-532-8
KEGG	C20713
PubChem CID	9898279
UNII	7413S0WMH6
CompTox Dashboard (EPA)	DTXSID401316929
InChI InChI=1S/C54H92O23/c1-23(2)10-9-14-54(8,77-48-44(69)40(65)37(62)29(74-48)22-70-46-42(67)38(63)34(59)26(19-55)71-46)24-11-16-53(7)33(24)25(58)18-31-51(5)15-13-32(50(3,4)30(51)12-17-52(31,53)6)75-49-45(41(66)36(61)28(21-57)73-49)76-47-43(68)39(64)35(60)27(20-56)72-47/h10,24-49,55-69H,9,11-22H2,1-8H3/t24-,25+,26+,27+,28+,29+,30-,31+,32-,33-,34+,35+,36+,37+,38-,39-,40-,41-,42+,43+,44+,45+,46+,47-,48-,49-,51-,52+,53+,54-/m0/s1 Key: GZYPWOGIYAIIPV-JBDTYSNRSA-N
SMILES CC(=CCC[C@@](C)([C@H]1CC[C@@]2([C@@H]1[C@@H](C[C@H]3[C@]2(CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)C)O)C)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO)O)O)O)O)O)O)C
Properties
Chemical formula	C₅₄H₉₂O₂₃
Molar mass	1109.307 g·mol⁻¹
Hazards
GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H302, H312, H332
Precautionary statements	P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references