Disposition of RS-26306, a potent luteinizing hormone-releasing hormone antagonist, in monkeys and rats after single intravenous and subcutaneous administration.

R L Chan; S C Hsieh; P E Haroldsen; W Ho; J J Nestor

Article Information

vol. 19 no. 5 858-864

PubMed

1686228

Published By

American Society for Pharmacology and Experimental Therapeutics

Print ISSN

0090-9556

Online ISSN

1521-009X

History

Published online September 1, 1991.

Author Information

R L Chan,
S C Hsieh,
P E Haroldsen,
W Ho and
J J Nestor, Jr

Department of Drug Metabolism, Syntex Research, Palo Alto, CA 94304.

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Disposition of RS-26306, a potent luteinizing hormone-releasing hormone antagonist, in monkeys and rats after single intravenous and subcutaneous administration.

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Article usage: April 1999 to June 2022

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Disposition of RS-26306, a potent luteinizing hormone-releasing hormone antagonist, in monkeys and rats after single intravenous and subcutaneous administration.

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Disposition of RS-26306, a potent luteinizing hormone-releasing hormone antagonist, in monkeys and rats after single intravenous and subcutaneous administration.

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Disposition of RS-26306, a potent luteinizing hormone-releasing hormone antagonist, in monkeys and rats after single intravenous and subcutaneous administration.

Article Information

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Article usage: April 1999 to June 2022

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Disposition of RS-26306, a potent luteinizing hormone-releasing hormone antagonist, in monkeys and rats after single intravenous and subcutaneous administration.

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Disposition of RS-26306, a potent luteinizing hormone-releasing hormone antagonist, in monkeys and rats after single intravenous and subcutaneous administration.

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