Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 193313생성일: 2026년 10월 24일
7-케토-데하이드로에피안드로스테론
7-케토-데하이드로에피안드로스테론 · 7-KETO DHEA · 7-Oxo-DHEA · 7-Ketoprasterone · 7-KETO DHEA, HPLC 98% · ABiraterone Impurity I · 7-Keto DHEA (Standard) · 7-keto DHEA(7-Oxo DHEA)
https://huagongshe.com/ko/chemical/193313
식별자 및 물리적 특성
| CAS No. | 566-19-8 |
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| 분자식 | C19H26O3 |
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| 평균 분자량 | 302.4 g/mol |
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| 단동위원소 질량 | 302.18819469 g/mol |
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| SMILES | C[C@]12CC[C@H](O)CC1=CC(=O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12 |
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| InChIKey | KPRGOTLNGIBVFL-GINZOMEDSA-N |
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| PubChem CID | 193313 |
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| ChEMBL | CHEMBL1875999 |
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| ChEBI | CHEBI:183808 |
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| EC No. | 111-754-6 |
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| DTXSID | DTXSID801024029 |
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| 현지명 | 7-케토-데하이드로에피안드로스테론 |
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화학 및 물리적 성질
| XLogP | 2 |
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| 극성 표면적 | 54.4 |
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| 수소 결합 공여자 수 | 1 |
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| 수소 결합 수용자 수 | 3 |
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| 회전 가능 결합 수 | 0 |
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| 무거운 원자 수 | 22 |
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| 형식 전하 | 0 |
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| 복잡도 | 577 |
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| 녹는점 | 245-248 °C |
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| 끓는 점 | 477.1±45.0 °C(Predicted) |
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| 밀도 | 1.19±0.1 g/cm3(Predicted) |
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| 용해도 | DMF: 25 mg/mlDMF:PBS(pH 7.2)(1:1): 0.5 mg/mlDMSO: 15 mg/mlEthanol: 10 mg/ml |
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| 물리적 상태 | 결정성 고체 |
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| pKa(산도 계수) | 14.67±0.60(Predicted) |
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| InChI | InChI=1/C19H26O3/c1-18-7-5-12(20)9-11(18)10-15(21)17-13-3-4-16(22)19(13,2)8-6-14(17)18/h10,12-14,17,20H,3-9H2,1-2H3/t12-,13-,14-,17-,18-,19-/s3 |
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| InChIKey | KPRGOTLNGIBVFL-YQJRJXGQNA-N |
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| SMILES | C[C@]12CC[C@H](O)CC1=CC(=O)[C@@]1([H])[C@]3([H])CCC(=O)[C@@]3(C)CC[C@]21[H] |&1:1,4,11,13,19,23,r| |
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안전 및 규제
| GHS 분류 | DangerH351 (100%): Suspected of causing cancer [Warning Carcinogenicity]P203, P280, P318, P405, and P501 (click each P-code to see the statement)The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory. |
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| Hazard Classes and Categories | Carc. 2 (100%) |
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용도
개요
7-Ketodehydroepiandrosterone (7-Keto-dehydroepiandrosterone; 7-keto-DHEA), chemically known under 3-acetyl-7-oxo-dehydroepiandrosterone, is a naturally occurring metabolite of the steroid hormone dehydroepiandrosterone (DHEA) and is marketed as such an anti-obesity dietary supplement. The synthesis of 7-keto-DHEA begins with an irreversible hydroxylation of DHEA in the position C7 by cytochrome P450 7B1 (CYP7B1) under the formation of 7 α-hydroxy-dehydroepiandrosterone (7 α-OH-DHEA). β-hydroxysteroid dehydrogenase type 1 (11 β-HSD 1) then catalyzes the interconversion of 7 α-OH-DHEA and 7 β-hydroxy-dehydroepiandrosterone (7 β-OH-DHEA) through a 7-keto-DHEA intermediary. DHEA is a "parent hormone" produced by glands near the kidneys. However, unlike DHEA, 7-keto-DHEA is not converted to steroid hormones such as androgen and estrogen. Taking 7-keto-DHEA by mouth or applying it to the skin does not increase the level of steroid hormones in the blood. People take 7-keto-DHEA for obesity, muscle strength, anxiety, depression, and other conditions. However, there is no good scientific evidence to support these uses[1].