Determine the necessary mass, volume, or concentration for preparing a solution.
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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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M303878-50mg
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50mg |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$66.90
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M303878-250mg
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250mg |
1
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$71.90
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M303878-1g
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1g |
3
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$236.90
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M303878-5g
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5g |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$1,066.90
|
|
| Synonyms | Medroxyprogesteron | Opera_ID_433 | 17-Hydroxy-6a-methylprogesterone | medroxyprogesterone | (6alpha)-17-hydroxy-6-methylpregn-4-ene-3,20-dione | C07119 | Medroxy Progesterone | Medroxyprogesteronum (INN-Latin) | MLS000069571 | Tox21_113401 | MEDROXYPROGE |
|---|---|
| Specifications & Purity | Moligand™, ≥98% |
| Storage Temp | Room temperature,Desiccated |
| Shipped In | Normal |
| Grade | Moligand™ |
| Action Type | AGONIST |
| Mechanism of action | Agonist of Progesterone receptor |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Steroids and steroid derivatives |
| Subclass | Pregnane steroids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Gluco/mineralocorticoids, progestogins and derivatives |
| Alternative Parents | 20-oxosteroids 3-oxo delta-4-steroids 17-hydroxysteroids Delta-4-steroids Cyclohexenones Tertiary alcohols Alpha-hydroxy ketones Cyclic alcohols and derivatives Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homopolycyclic compounds |
| Substituents | Progestogin-skeleton - 20-oxosteroid - 3-oxo-delta-4-steroid - 3-oxosteroid - 17-hydroxysteroid - Oxosteroid - Hydroxysteroid - Delta-4-steroid - Cyclohexenone - Alpha-hydroxy ketone - Cyclic alcohol - Tertiary alcohol - Cyclic ketone - Ketone - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Alcohol - Organooxygen compound - Organic oxide - Aliphatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as gluco/mineralocorticoids, progestogins and derivatives. These are steroids with a structure based on a hydroxylated prostane moiety. |
| External Descriptors | C21 steroids (gluco/mineralocorticoids, progestogins) and derivatives |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Pubchem Sid | 504751978 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751978 |
| IUPAC Name | (6S,8R,9S,10R,13S,14S,17R)-17-acetyl-17-hydroxy-6,10,13-trimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one |
| INCHI | InChI=1S/C22H32O3/c1-13-11-16-17(20(3)8-5-15(24)12-19(13)20)6-9-21(4)18(16)7-10-22(21,25)14(2)23/h12-13,16-18,25H,5-11H2,1-4H3/t13-,16+,17-,18-,20+,21-,22-/m0/s1 |
| InChIKey | FRQMUZJSZHZSGN-HBNHAYAOSA-N |
| Smiles | CC1CC2C(CCC3(C2CCC3(C(=O)C)O)C)C4(C1=CC(=O)CC4)C |
| Isomeric SMILES | C[C@H]1C[C@@H]2[C@H](CC[C@]3([C@H]2CC[C@@]3(C(=O)C)O)C)[C@@]4(C1=CC(=O)CC4)C |
| Molecular Weight | 344.5 |
| Reaxy-Rn | 3438589 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3438589&ln= |
| Solubility | Insoluble in water; Degree of Solubility in water: 2.95 mg/l 25 °C; Very soluble in Chloroform |
|---|---|
| Specific Rotation[α] | 75° (C=1,CHCl3) |
| Melt Point(°C) | 217 °C |
| Molecular Weight | 344.500 g/mol |
| XLogP3 | 3.500 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 344.235 Da |
| Monoisotopic Mass | 344.235 Da |
| Topological Polar Surface Area | 54.400 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 664.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 7 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Min Liu, Yong-Jie Mi, Juan Dai. (2023) Aquaporin 7 is upregulated through the PI3K-Akt pathway and modulates decidualisation of endometrial stromal cells. REPRODUCTION FERTILITY AND DEVELOPMENT, 35 (14): (669-675). |
| 2. Xiaomei Chen, Liulin Wei, Qian Liu, Xueyun Gao, Jingchan Zhao. (2023) Application of temperature-sensitive hyperbranched polysiloxanes for the determination of polycyclic aromatic hydrocarbons in foodstuffs. MICROCHEMICAL JOURNAL, 194 (109364). |