12 Results for "

20-lyase

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "20-lyase" in MCE Product Catalog:

24
24 Cited Publications
Cat. No.: HY-70013
CAS No.: 154229-19-3
Synonyms: CB-7598
Target:  

Cytochrome P450

Research Areas:  

Cancer

Abiraterone is a potent and irreversible CYP17A1 inhibitor with antiandrogen activity, which inhibits both the 17α-hydroxylase and 17,20-lyase activity of the cytochrome p450 enzyme CYP17 with IC50s of 2.5 nM and 15 nM, respectively.
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2
2 Cited Publications
Cat. No.: HY-10505
CAS No.: 566939-85-3
Purity:  99.70%
Synonyms: TAK-700
Target:  

Cytochrome P450

Research Areas:  

Cancer

Orteronel (TAK-700) is a highly selective inhibitor of human 17,20-lyase (CYP17) with IC50 of 38 nM, and exhibits >1000-fold selectivity over other CYPs such as 11-hydroxylase and CYP3A4 .
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Cat. No.: HY-70013S
CAS No.: 2122245-62-7
Synonyms: CB-7598-d4
Abiraterone-d4 is the deuterium labeled Abiraterone. Abiraterone is a potent and irreversible CYP17A1 inhibitor with antiandrogen activity, which inhibits both the 17α-hydroxylase and 17,20-lyase activity of the cytochrome p450 enzyme CYP17 with IC50s of 2.5 nM and 15 nM, respectively.
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Cat. No.: HY-148430
CAS No.: 121768-39-6
Purity:  99.83%
Target:  

Cytochrome P450

Research Areas:  

Cancer

4-Pyridylmethyl adamantanecarboxamide (Compound 11) is an Aromatase inhibitor with an IC50 of 1.5 μM against hAromatase. 4-Pyridylmethyl adamantanecarboxamide inhibits the C17,20-lyase activity of testicular cytochrome P45017α with an IC50 of 1600 nM, and also inhibits the 17α-hydroxylase activity of this enzyme with an IC50 of 7700 nM. 4-Pyridylmethyl adamantanecarboxamide can be used in the research of prostate cancer .
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Cat. No.: HY-120067
CAS No.: 183012-13-7
Target:  

Cytochrome P450

Research Areas:  

Endocrinology

YM116 is an orally active and competitive CYP17A1 (17,20-lyase) inhibitor (Ki: 0.38 nM). YM116 reduces the synthesis of adrenal androgens by preferentially inhibiting C17-20 lyase activity. YM116 decreases the serum testosterone concentration, reduces dehydroepiandrosterone sulfate levels and decreases prostatic weights .
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Cat. No.: HY-156481
CAS No.: 2126-63-8
Target:  

Cytochrome P450

Research Areas:  

Others

SU-8000 is an inhibitor that selectively targets 17α-hydroxylase and C17-20-lyase in rat testes. When administered to pregnant rats, SU-8000 can cause hypospadias in male fetuses .
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Cat. No.: HY-70013R
CAS No.: 154229-19-3
Synonyms: CB-7598 (Standard)
Research Areas:  

Cancer

Abiraterone (Standard) is the analytical standard of Abiraterone. This product is intended for research and analytical applications. Abiraterone is a potent and irreversible CYP17A1 inhibitor with antiandrogen activity, which inhibits both the 17α-hydroxylase and 17,20-lyase activity of the cytochrome p450 enzyme CYP17 with IC50s of 2.5 nM and 15 nM, respectively.
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Cat. No.: HY-E71368
Research Areas:  

Others

17α-Hydroxyprogesterone deacetylase (EC 1.14.14.32) is a cytochrome P450 enzyme that exhibits 17,20-lyase activity. It participates in catalyzing the 17-hydroxylation of pregnenolone and progesterone.
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Cat. No.: HY-P85566
Synonyms: 20 lyase; CP17A_HUMAN; CPT7; CYP17; CYP17A1; CYPXVII; Cytochrome P450 17A1; Cytochrome P450 family 17; Cytochrome P450 family 17 subfamily A polypeptide 1; Cytochrome p450 subfamily XVII; steroid 17 alpha hydroxylase; adrenal hyperplasia; Cytochrome p450 XVIIA1; Cytochrome P450-C17; Cytochrome P450c17; OTTHUMP00000020382; P450 C17; P450c17; S17AH; Steroid 17 alpha hydroxylase/17,20 lyase; Steroid 17 alpha monooxygenase; Steroid 17-alpha-hydroxylase/17; Steroid 17-alpha-monooxygenase.

Host:  

Mouse

Application:  

WB

Reactivity:  

Human

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Cat. No.: HY-Z14322
CAS No.: 2174-13-2
Target:  

Tyrosine Hydroxylase

Research Areas:  

Cancer

(3β)-3-(Acetyloxy)pregna-5,16-dien-20-one 20-oxime is a human 17α-hydroxylase/C17,20-lyase (P45017α) inhibitor with a human IC50 of 67 nM and a rat IC50 of 2754 nM. (3β)-3-(Acetyloxy)pregna-5,16-dien-20-one 20-oxime blocks the human testicular microsomal enzyme mediating androgen biosynthesis steps. (3β)-3-(Acetyloxy)pregna-5,16-dien-20-one 20-oxime does not inhibit human 5α-reductase in prostatic microsomes .
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Cat. No.: HY-10505R
CAS No.: 566939-85-3
Synonyms: TAK-700 (Standard)
Research Areas:  

Cancer

Orteronel (Standard) is the analytical standard of Orteronel (HY-10505). This product is intended for research and analytical applications. Orteronel (TAK-700) is a highly selective inhibitor of human 17,20-lyase (CYP17) with IC50 of 38 nM, and exhibits >1000-fold selectivity over other CYPs such as 11-hydroxylase and CYP3A4 .
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Cat. No.: HY-136745
CAS No.: 331684-05-0
Target:  

Cytochrome P450

Research Areas:  

Cancer

Aromatase-IN-1 is a competitive aromatase (P450arom) inhibitor with a human IC50 of 40 nM and a Ki of 1.05 nM. Aromatase-IN-1 binds via coordination of imidazole nitrogen to the heme iron of aromatase. Aromatase-IN-1 can be used for the research of breast cancer .
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