HIV-1 integrase inhibitor 8 - 99%, high purity , CAS No.1568-80-5

  • ≥99%
Item Number
H650812
Grouped product items
SKUSizeAvailabilityPrice Qty
H650812-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$50.90
H650812-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$80.90

Basic Description

Synonyms1,1,1',1'-tetramethyl-3,3'-spirobi[2H-indene]-5,5'-diol | 3,3,3',3'-Tetramethyl-1,1'-spirobi(indan)-6,6'-diol | Phenyl butyl ether | 1,1'-Spirobi[1H-indene]-6,6'-diol,2,2',3,3'-tetrahydro-3,3,3',3'-tetramethyl- | 3,3,3',3'-tetramethyl-2,2',3,3'-tetrahydro
Specifications & Purity≥99%
Biochemical and Physiological MechanismsHIV-1 integrase inhibitor 8 is a HIV-1 integrase inhibitor, compound 8.
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

HIV-1 integrase inhibitor 8 is a HIV-1 integrase inhibitor, compound 8.

In Vitro

HIV-1 integrase inhibitor 8 is against 3′-processing (TC) and strand-transfer (ST) activities in the presence of Mn 2+ as the cationic cofactor by gel assay with IC 50 values of 275 µM and 200 µM, respectively. It inhibits the strand-transfer (ST) activity with an IC 50 value of 200 µM. The DNA relaxation activity of MCV topoisomerase is monitored by gel electrophoresis, while DNA cleavage and religation activities were monitored using a microtiter assay. HIV-1 integrase inhibitor 8 inhibits MCV topoisomerase and DNA religation with IC 50 values of 500 µM and 200 µM, respectively. This result demonstrates that compound 8 is inactive against topoisomerase in both assays. HIV-1 integrase inhibitor 8 induces cell cytotoxicity and yields a LD 50 (dose at which the signal is reduced 50% due to cell death) of 20 μM in HeLa cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

Associated Targets(Human)

HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

pol Human immunodeficiency virus type 1 protease (9113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Molluscum contagiosum virus (31 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human immunodeficiency virus 1 (70413 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 1,1,1',1'-tetramethyl-3,3'-spirobi[2H-indene]-5,5'-diol
INCHI InChI=1S/C21H24O2/c1-19(2)11-21(17-9-13(22)5-7-15(17)19)12-20(3,4)16-8-6-14(23)10-18(16)21/h5-10,22-23H,11-12H2,1-4H3
InChi Key SICLLPHPVFCNTJ-UHFFFAOYSA-N
Canonical SMILES CC1(CC2(CC(C3=C2C=C(C=C3)O)(C)C)C4=C1C=CC(=C4)O)C
Isomeric SMILES CC1(CC2(CC(C3=C2C=C(C=C3)O)(C)C)C4=C1C=CC(=C4)O)C
Alternate CAS 1568-80-5
PubChem CID 74071
Molecular Weight 308.4

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilityDMSO : 125 mg/mL (405.30 mM; Need ultrasonic)

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