CTN-986
CTN-986
Names
IUPAC name
3′,4′,5,7-Tetrahydroxy-3-{[3-C -(hydroxymethyl)-β-D -erythrofuranosyl]-(1→2)-[α-L -rhamnopyranosyl-(1→6)]-β-D -glucopyranosyloxy}flavone
Systematic IUPAC name
(42 S ,43 R ,44 S ,45 S ,46 R ,72 R ,73 R ,74 R ,75 R ,76 S )-43 -{[(2S ,3R ,4R )-3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-13 ,14 ,25 ,27 ,44 ,45 ,73 ,74 ,75 -nonahydroxy-76 -methyl-24 H -3,6-dioxa-2(2,3)-[1]benzofurana-4(2,6),7(2)-bis(oxana)-1(1)-benzenaheptaphane-24 -one
Other names
3-[(
O -
D -
apio -β-
D -furanosyl-(1→2)-
O -[6-deoxy-α-
L -
mannopyranosyl -(1→6)]-β-
D -
glucopyranosyl )oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4
H -1-benzopyran-4-one
Quercetin 3-O-b-d-apiofuranosyl-(1→2)-[a-l-rhamnopyranosyl-(1→6)]-b-d-glucopyranoside
Identifiers
ChemSpider
UNII
InChI=1S/C32H38O20/c1-10-19(38)22(41)24(43)29(48-10)46-7-17-20(39)23(42)27(52-31-28(44)32(45,8-33)9-47-31)30(50-17)51-26-21(40)18-15(37)5-12(34)6-16(18)49-25(26)11-2-3-13(35)14(36)4-11/h2-6,10,17,19-20,22-24,27-31,33-39,41-45H,7-9H2,1H3/t10-,17+,19-,20+,22+,23-,24+,27+,28-,29+,30-,31-,32+/m0/s1
Key: UPVDFUGORYNXMW-VCKCKQTPSA-N
InChI=1/C32H38O20/c1-10-19(38)22(41)24(43)29(48-10)46-7-17-20(39)23(42)27(52-31-28(44)32(45,8-33)9-47-31)30(50-17)51-26-21(40)18-15(37)5-12(34)6-16(18)49-25(26)11-2-3-13(35)14(36)4-11/h2-6,10,17,19-20,22-24,27-31,33-39,41-45H,7-9H2,1H3/t10-,17+,19-,20+,22+,23-,24+,27+,28-,29+,30-,31-,32+/m0/s1
Key: UPVDFUGORYNXMW-VCKCKQTPBC
OC1=CC(O)=C(C(C(O[C@H]2[C@H](O[C@@]3([H])[C@H](O)[C@@](O)(CO)CO3)[C@@H](O)[C@H](O)[C@@H](CO[C@H]4[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O4)O2)=C(C5=CC=C(O)C(O)=C5)O6)=O)C6=C1
Properties
C 32 H 38 O 20
Molar mass
742.636 g·mol−1
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
CTN-986 is a glycoside of quercetin found in cottonseeds and cottonseed oil . In a rodent model , it displays some antidepressant -like properties and stimulation of neurogenesis in the hippocampus .[ 1] The neurogenesis appears to be mediated by activation of the 5-HT1A receptor , as co-administration with the 5-HT1A antagonist WAY-100,635 abolished the effect.[ 1]
See also
References
^ a b Zhang LM, Zhang YZ, Liu YQ, Gong ZH, Zhao YM, Li YF (2009). "CTN-986, a compound extracted from cottonseeds, increases cell proliferation in hippocampus in vivo and in cultured neural progenitor cells in vitro". Eur J Pharmacol . 607 (1–3): 110–113. doi :10.1016/j.ejphar.2008.12.052 . PMID 19326568 .
Flavonols and their conjugates
Backbone
Flavonols
O -Methylated flavonols
Derivative flavonols
Pyranoflavonols
Furanoflavonols
Semisynthetic
SSRIs Tooltip Selective serotonin reuptake inhibitors SNRIs Tooltip Serotonin–norepinephrine reuptake inhibitors NRIs Tooltip Norepinephrine reuptake inhibitors NDRIs Tooltip Norepinephrine–dopamine reuptake inhibitors NaSSAs Tooltip Noradrenergic and specific serotonergic antidepressants SARIs Tooltip Serotonin antagonist and reuptake inhibitors SMS Tooltip Serotonin modulator and stimulators Others
TCAs Tooltip Tricyclic antidepressants TeCAs Tooltip Tetracyclic antidepressants Others
Non-selective MAOA Tooltip Monoamine oxidase A -selectiveMAOB Tooltip Monoamine oxidase B -selective