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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224325Generated: October 31, 2026

Allobarbital → HCID 86737309, compound

https://huagongshe.com/reaction/224325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllobarbitalHCID 5842—
ReactantHCID 86737310HCID 86737310—
ProductHCID 86737309HCID 86737309—

Reaction Steps

For example, in standard laboratory tests, (i) by intravenous administration to the allobarbital anaesthetized dog, (5Z,13E)-(9α,11α,15S)-6,9-epoxy-11,15-dihydroxy-20-chloroprosta-5,13-dienoic acid methyl ester produces a fall in blood pressure of 14 mmHg and 34 mmHg lasting 4 and 5 minutes at the doses of 0.1 and 0.2 μg/kg animal body weight, respectively, (5Z,13E)-(9α,11α,15S,16RS)-6,9-epoxy-11,15-dihydroxy-16-methyl-20-chloroprosta-5,13-dienoic acid methyl ester produces a fall in blood pressure of 20 mmHg and 48 mmHg lasting 11 and 15 minutes at the doses of 0.1 and 0.2 μg/kg animal body weight, respectively, (5Z,13E)-(9α,11α,15S,17R)-6,9-epoxy-11,15-dihydroxy-17-methyl-20-chloroprosta-5,13-dienoic acid methyl ester produces a fall in blood pressure of 10 mmHg lasting 3 minutes at the dose of 100 μg/kg animal body weight, (5Z,13E)-(9α,11α,15R)-6,9-epoxy-11,15-dihydroxy-15-[1-(4-fluorobutyl)cyclobutyl]-16,17,18,19,20-pentanorprosta-5,13-dienoic acid methyl ester produces a fall in blood pressure of 24 mmHg, 40 mmHg and 52 mmHg lasting 8, 20 and 15 minutes at the doses of 1, 2 and 4 μg/kg animal body weight, respectively, and (5Z,13E)-(9α,11α,15S)-6,9-epoxy-11,15-dihydroxy-15-[3-(2-chloroethyl)cyclopentyl]-16,17,18,19,20-pentanorprosta-5,13-dienoic acid methyl ester produces a fall in blood pressure of 22 mmHg, 32 mmHg and 50 mmHg lasting 9, 11 and 15 minutes at the doses of 0.1, 0.2 and 0.4 μg/kg animal body weight, respectively, (ii) (5Z,13E)-(9α,11α,15S)-6,9-epoxy-11,15-dihydroxy-20-chloroprosta-5,13-dienoic acid methyl ester, (5Z,13E)-(9α,11α,15S,16RS)-6,9-epoxy-11,15-dihydroxy-16-methyl-20-chloroprosta-5,13-dienoic acid methyl ester, (5Z,13E)-(9α,11α,15S,17R)-6,9-epoxy-11,15-dihydroxy-17-methyl-20-chloroprosta-5,13-dienoic acid methyl ester, (5Z,13E)-(9α,11α,15R)-6,9-epoxy-11,15-dihydroxy-15-[1-(4-fluorobutyl)cyclobutyl]-16,17,18,19,20-pentanorprosta-5,13-dienoic acid methyl ester and (5Z,13E)-(9α,11α,15S)-6,9-epoxy-11,15-dihydroxy-15-[3-(2-chloroethyl)cyclopentyl]-16,17,18,19,20-pentanorprosta-5,13-dienoic acid methyl ester produce a 50% inhibition of adenosine diphosphate-induced blood platelet aggregation in platelet-rich plasma of rats at the concentrations of 4.0×10-3, 1.5×10-3, 3.3×10-3, 1.8×10-2 and 2.3×10-3 μg/ml, respectively, in comparison with controls, and (iii) (5Z,13E)-(9α,11α,15S,16RS)-6,9-epoxy-11,15-dihydroxy-16-methyl-20-chloroprosta-5,13-dienoic acid methyl ester and (5Z,13E)-(9α,11α,15R)-6,9-epoxy-11,15-dihydroxy-15-[1-(4-fluorobutyl)cyclobutyl]-16,17,18,19,20-pentanorprosta-5,13-dienoic acid methyl ester stimulate uterine contraction in the pregnant female rat when administered intravenously on the 20th day of gestation at the doses of 10 and 10-20 μg/kg animal body weight, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04232009
Source datasetuspto-grants-1980_11
ORD IDord-2a5a2f21f2754f64bd9870f53de3e198
Source noteuspto-grants-1980_11