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S-pentachlorobutadienyl-L-cysteine

(2R)-2-amino-3-[(1E)-1,2,3,4,4-pentachlorobuta-1,3-dienyl]sulfanylpropanoic acid · also: (S-pentachlorobutadienyl)-l-cysteine, S-Pentachlorobuta-1,3-dien-yl-cysteine, S-(1,2,3,4,4-Pentachloro-1,3-butadienyl)-L-cysteine, 5-(1,2,3,4,4-pentachloro-1,3-butadienyl)-L-cysteine, S-(1,2,3,4,4-pentachloro-1,3- butadienyl)-L-cysteine

FormulaC7H6Cl5NO2S
Mol. weight345.44
PubChem CID3033729
InChIKeyGEAIQETWXSVTMO-KEZSNRNCSA-N
SMILESC([C@@H](C(=O)O)N)S/C(=C(/C(=C(Cl)Cl)Cl)\Cl)/Cl
530Patents
24Research papers
359Patents - last 3 years
4Papers - last 3 years

Who owns the IP

The organizations most actively patenting around this compound, ranked by referenced patent volume.

#AssigneePatents
1Every Co42
2Beijing Academy of Agriculture and Forestry Sciences17
3Institute of Genetics and Developmental Biology11
4Anhui Agricultural University7
5International Business Machines Corp7
6NantHealth Inc4
7Nantomics LLC4
8Tianjin Institute of Industrial Biotechnology4
9Center for Excellence in Molecular Plant Sciences3
10Institute of Botany3

Explore the full landscape

This preview shows the leading assignees. Cypris reveals the full ownership landscape - every filing entity, filing trends, and portfolio momentum.

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Where innovation is concentrated

Patent classifications ranked by volume reveal the technical domains with the most active filing.

#CodeAreaPatents
1C12NMicroorganisms, enzymes394
2C07KPeptides302
3Y02AClimate change adaptation100
4C12YEnzyme nomenclature (EC numbers)91
5C12QMeasuring/testing involving enzymes57
6A23LFoods and beverages (general)40
7A23J35
8G06F32
9C12PFermentation, enzyme processes31
10H04L29

AI mapped opportunity space

This preview shows where patent activity concentrates. Cypris maps the full classification landscape to surface technical whitespace and IP headroom.

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Where research is gaining momentum

Research themes ranked by publication activity show where scientific interest is accelerating around this compound.

#Research topicPapers
1Organoselenium and organotellurium chemistry1

Who's driving the science

The most-published authors working with this compound, alongside their primary affiliations.

#AuthorAffiliationPapers
1Edward A. LockSyngenta (United Kingdom)7
2Rick G. SchnellmannUniversity of Georgia5
3Spyridon VamvakasUniversity of Würzburg4
4Alf WallinKarolinska Institutet2
5Carlotta E. GrovesUniversity of Georgia2
6D. HenschlerUniversity of Würzburg2
7James StevensW. Alton Jones Cell Science Center2
8Thomas W. JonesUniversity of Maryland, Baltimore2
9W. DekantUniversity of Würzburg2
10Wolfgang DekantUniversity of Würzburg2

Research leaders

This preview lists the top authors. Cypris surfaces the full researcher landscape, their affiliations, and how scientific influence is shifting.

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The literature that defines it

The most-cited papers anchoring the scientific record for this compound.

Frequently asked questions

Common questions about this compound's patent and research landscape, answered from the underlying data.

What is the molecular formula and weight of S-pentachlorobutadienyl-L-cysteine?

S-pentachlorobutadienyl-L-cysteine has the molecular formula C7H6Cl5NO2S and a molecular weight of 345.44.

Which organization has filed the most patents related to this compound?

Every Co has filed the most patents related to this compound, with 42 patent filings.

Who is the most prolific author publishing on this compound, and what is their affiliation?

Edward A. Lock from Syngenta (United Kingdom) is the most prolific author on this compound, with 7 papers published.

What is the primary patent classification category for inventions related to this compound?

The primary patent classification is C12N, which has the highest count with 394 patents related to this compound.

What was the main focus of early research on this compound's biological effects?

Early research focused on the nephrotoxicity and mitochondrial toxicity of this compound. A 1983 study examined in vivo and in vitro nephrotoxicity, while 1987 studies investigated its toxicity to rabbit renal proximal tubules and its effects on isolated rat renal cortical mitochondria, including its ability to uncouple oxidative phosphorylation.

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