MedKoo Cat#: 593019 | Name: Atizoram
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Atizoram, or CP-80,633, is a cyclic nucleotide phosphodiesterase (PDE4) inhibitor, has been shown to augment intracellular cAMP levels and to inhibit TNFalpha release from human monocytes in vitro.

Chemical Structure

Atizoram
Atizoram
CAS#135637-46-6

Theoretical Analysis

MedKoo Cat#: 593019

Name: Atizoram

CAS#: 135637-46-6

Chemical Formula: C18H24N2O3

Exact Mass: 316.1787

Molecular Weight: 316.40

Elemental Analysis: CC, 68.33; H, 7.65; N, 8.85; O, 15.17

Price and Availability

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1mg USD 250.00 2 Weeks
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Related CAS #
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Synonym
Atizoram; CP 80,633; CP-80,633; CP80,633; CP 80633; CP80633; CP-80633
IUPAC/Chemical Name
Tetrahydro-5-(4-methoxy-3-((1S,2S,4R)-2-norbomyloxy)phenyl)-2(1H)-pyrimidinone
InChi Key
LITNEAPWQHVPOK-FFSVYQOJSA-N
InChi Code
InChI=1S/C18H24N2O3/c1-22-15-5-4-12(14-9-19-18(21)20-10-14)8-17(15)23-16-7-11-2-3-13(16)6-11/h4-5,8,11,13-14,16H,2-3,6-7,9-10H2,1H3,(H2,19,20,21)/t11-,13+,16+/m1/s1
SMILES Code
COc1c(O[C@H]2C[C@@H]3CC[C@H]2C3)cc(C4CNC(NC4)=O)cc1
Appearance
Solid powder
Purity
>95% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 316.40 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Turner CR, Cohan VL, Cheng JB, Showell HJ, Pazoles CJ, Watson JW. The in vivo pharmacology of CP-80, 633, a selective inhibitor of phosphodiesterase 4. J Pharmacol Exp Ther. 1996 Sep;278(3):1349-55. PMID: 8819522. 2: Cheng JB, Watson JW, Pazoles CJ, Eskra JD, Griffiths RJ, Cohan VL, Turner CR, Showell HJ, Pettipher ER. The phosphodiesterase type 4 (PDE4) inhibitor CP-80,633 elevates plasma cyclic AMP levels and decreases tumor necrosis factor- alpha (TNFalpha) production in mice: effect of adrenalectomy. J Pharmacol Exp Ther. 1997 Feb;280(2):621-6. PMID: 9023272. 3: Wright KF, Turner CR, Jayasinghe-Beck R, Cohen VL, Cheng JB, Watson JW. Differential in vivo and in vitro bronchorelaxant activities of CP-80,633, a selective phosphodiesterase 4 inhibitor. Can J Physiol Pharmacol. 1997 Aug;75(8):1001-8. PMID: 9360015. 4: Mezzani A, Corrà U, Giordano A, Colombo S, Psaroudaki M, Giannuzzi P. Upper intensity limit for prolonged aerobic exercise in chronic heart failure. Med Sci Sports Exerc. 2010 Apr;42(4):633-9. doi: 10.1249/MSS.0b013e3181bdc69d. PMID: 19952837. 5: Hao L, Wang LS, Liu Y, Wang T, Guo HL, Pan J, Wang D, Bi YW, Ji JT, Xin L, Du TT, Lin JH, Zhang D, Zeng XP, Zou WB, Chen H, Xie T, Li BR, Liao Z, Cong ZJ, Xu ZL, Li ZS, Hu LH. The different course of alcoholic and idiopathic chronic pancreatitis: A long-term study of 2,037 patients. PLoS One. 2018 Jun 8;13(6):e0198365. doi: 10.1371/journal.pone.0198365. PMID: 29883461; PMCID: PMC5993321. 6: Das NG, Huque KS, Amanullah SM, Dharmapuri S, Makkar HPS. Study of chemical composition and nutritional values of vegetable wastes in Bangladesh. Vet Anim Sci. 2018 Mar 2;5:31-37. doi: 10.1016/j.vas.2018.02.003. PMID: 32734043; PMCID: PMC7386774. 7: Cohan VL, Showell HJ, Fisher DA, Pazoles CJ, Watson JW, Turner CR, Cheng JB. In vitro pharmacology of the novel phosphodiesterase type 4 inhibitor, CP-80633. J Pharmacol Exp Ther. 1996 Sep;278(3):1356-61. 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