MedKoo Cat#: 414614 | Name: Org 31806

Description:

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

Org 31806 is a progestational hormone antagonist.

Chemical Structure

Org 31806
Org 31806
CAS#123916-70-1

Theoretical Analysis

MedKoo Cat#: 414614

Name: Org 31806

CAS#: 123916-70-1

Chemical Formula: C30H39NO2

Exact Mass: 445.2981

Molecular Weight: 445.65

Elemental Analysis: C, 80.86; H, 8.82; N, 3.14; O, 7.18

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
Org 31806; Org31806; Org-31806
IUPAC/Chemical Name
Spiro(estra-4,9-diene-17,2'(3'H)-furan)-3-one, 11-(4-(dimethylamino)phenyl)-4',5'-dihydro-7-methyl-, (7beta,11beta,17beta)-
InChi Key
WFPOBMHQGIPWFB-GCLUAJDJSA-N
InChi Code
InChI=1S/C30H39NO2/c1-19-16-21-17-23(32)10-11-24(21)28-25(20-6-8-22(9-7-20)31(3)4)18-29(2)26(27(19)28)12-14-30(29)13-5-15-33-30/h6-9,17,19,25-27H,5,10-16,18H2,1-4H3/t19-,25+,26-,27-,29-,30-/m0/s1
SMILES Code
C[C@@]12[C@@]3(OCCC3)CC[C@@]1([H])[C@]4([H])[C@@H](C)CC5=CC(CCC5=C4[C@@H](C6=CC=C(N(C)C)C=C6)C2)=O
Appearance
Solid powder
Purity
>98% (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
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 445.65 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: Kloosterboer HJ, Deckers GH, Schoonen WG. Pharmacology of two new very selective antiprogestagens: Org 31710 and Org 31806. Hum Reprod. 1994 Jun;9 Suppl 1:47-52. doi: 10.1093/humrep/9.suppl_1.47. PMID: 7962469. 2: Skinner DC. Org-31806 Organon NV. IDrugs. 1998 Jul;1(3):350-4. PMID: 18465560. 3: Dao B, Vanage G, Li XJ, Bardin CW, Koide SS. Comparative effectiveness of three antiprogestins alone and in combination with anordiol in terminating pregnancy in the rat. Contraception. 1997 Jan;55(1):35-40. doi: 10.1016/s0010-7824(96)00239-9. PMID: 9013059. 4: Mizutani T, Bhakta A, Kloosterboer HJ, Moudgil VK. Novel antiprogestins Org 31806 and 31710: interaction with mammalian progesterone receptor and DNA binding of antisteroid receptor complexes. J Steroid Biochem Mol Biol. 1992 Aug;42(7):695-704. doi: 10.1016/0960-0760(92)90110-5. PMID: 1504008. 5: Klijn JG, Setyono-Han B, Sander HJ, Lamberts SW, de Jong FH, Deckers GH, Foekens JA. Pre-clinical and clinical treatment of breast cancer with antiprogestins. Hum Reprod. 1994 Jun;9 Suppl 1:181-9. doi: 10.1093/humrep/9.suppl_1.181. PMID: 7962463. 6: Hurd C, Underwood B, Herman M, Iwasaki K, Kloosterboer HJ, Dinda S, Moudgil VK. Characterization of ligand binding, DNA binding and phosphorylation of progesterone receptor by two novel progesterone receptor antagonist ligands. Mol Cell Biochem. 1997 Oct;175(1-2):205-12. doi: 10.1023/a:1006827701940. PMID: 9350053. 7: Xiao E, Xia-Zhang L, Shanen D, Ferin M. Tonic support of luteinizing hormone secretion by adrenal progesterone in the ovariectomized monkey replaced with midfollicular phase levels of estradiol. J Clin Endocrinol Metab. 1997 Jul;82(7):2233-8. doi: 10.1210/jcem.82.7.4083. PMID: 9215299. 8: Iwasaki K, Underwood B, Herman M, Dinda S, Kodali S, Kloosterboer HJ, Hurd C, Moudgil VK. Effects of antiprogestins on the rate of proliferation of breast cancer cells. Mol Cell Biochem. 1999 Aug;198(1-2):141-9. doi: 10.1023/a:1006945813508. PMID: 10497889. 9: Koper JW, Molijn GJ, van Uffelen CJ, Stigter E, Lamberts SW. Antiprogestins and iatrogenic glucocorticoid resistance. Life Sci. 1997;60(9):617-24. doi: 10.1016/s0024-3205(96)00698-4. PMID: 9048964. 10: Bhakta A, Herman M, Levina IS, Moudgil VK. Interaction of cycloalkanoprogesterones with mammalian progesterone receptor: binding of pregna-D'-pentaranes in the calf uterine cytosol. Mol Cell Biochem. 1993 Aug 25;125(2):153-61. doi: 10.1007/BF00936444. PMID: 8283970.