A clickable form of cholic acid
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Clickable Cholic Acid

Item No. 40735

Technical Information
Formal Name
2-((R)-4-((3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-trihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanamido)pent-4-ynoic acid
Synonyms
  • Cholalic Acid
  • Cholalin
  • ClickTag™ Cholic Acid
Molecular Formula
C29H45NO6
Formula Weight
Purity
≥95%
A solid
DMSO: Soluble: ≥10 mg/mlEthanol: Soluble: ≥10 mg/ml
SMILES
C[C@H](CCC(NC(C(O)=O)CC#C)=O)[C@@]1([H])CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@@]21C
InChi Code
InChI=1S/C29H45NO6/c1-5-6-22(27(35)36)30-25(34)10-7-16(2)19-8-9-20-26-21(15-24(33)29(19,20)4)28(3)12-11-18(31)13-17(28)14-23(26)32/h1,16-24,26,31-33H,6-15H2,2-4H3,(H,30,34)(H,35,36)/t16-,17+,18-,19-,20+,21+,22?,23-,24+,26+,28+,29-/m1/s1
InChi Key
UDNHXSOLSNXBHY-OPZMEAEDSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Clickable cholic acid is a clickable form of the primary bile acid cholic acid (Item No. 20250). It has been used in the synthesis of bile acid-nucleoside conjugates with anticancer and antimycobacterial activities.1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Agarwal, D.S., Siva Krishna, V., Sriram, D., et alClickable conjugates of bile acids and nucleosides: Synthesis, characterization, in vitro anticancer and antituberculosis studies. Steroids 139, 35-44 (2018).