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Key Documents

A123

Sigma-Aldrich

R-(+)-p-Aminoglutethimide (+)-tartrate salt

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About This Item

Empirical Formula (Hill Notation):
C13H16N2O2 · C4H6O6
CAS Number:
Molecular Weight:
382.37
UNSPSC Code:
12352202
PubChem Substance ID:

Assay

99.4% (HPLC)

mp

124-127 °C

shipped in

ambient

SMILES string

O[C@H]([C@@H](O)C(O)=O)C(O)=O.CC[C@@]1(CCC(=O)NC1=O)c2ccc(N)cc2

InChI

1S/C13H16N2O2.C4H6O6/c1-2-13(8-7-11(16)15-12(13)17)9-3-5-10(14)6-4-9;5-1(3(7)8)2(6)4(9)10/h3-6H,2,7-8,14H2,1H3,(H,15,16,17);1-2,5-6H,(H,7,8)(H,9,10)/t13-;1-,2-/m11/s1

InChI key

DQUXPVVSVXIQNE-IMXLTCNTSA-N

Biochem/physiol Actions

Inhibitor of aromatases involved in conversion of androgens to estrogens, and thus useful in chemotherapy of hormone-sensitive tumors (e.g., breast cancer). Also inhibits corticosteroid biosynthesis, termed a "medical adrenalectomy."

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Martina Dieber-Rotheneder et al.
Journal of the Society for Gynecologic Investigation, 13(6), 435-441 (2006-08-02)
This study tested the hypothesis that the endothelin (ET)/ET receptor (ETR) system in biologic fluids and in the human placenta is altered in delayed miscarriages as compared to apparently normal early pregnancies (reference group). Immunoreactive ET (irET) concentrations were measured
E J Sanford et al.
The Journal of urology, 115(2), 170-174 (1976-02-01)
Complete adrenal suppression with aminoglutethimide has been accomplished in 7 patients with progressive stage D carcinoma of the prostate who had become refractory to orchiectomy and the administration of exogenous estrogens. A favorable response was noted in 3 patients. These

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