NCBI Taxonomy: 44924
Parazoanthus (ncbi_taxid: 44924)
found 83 associated metabolites at genus taxonomy rank level.
Ancestor: Parazoanthidae
Child Taxonomies: Parazoanthus axinellae, Parazoanthus swiftii, Parazoanthus darwini, Parazoanthus capensis, Parazoanthus elongatus, Parazoanthus atlanticus, Parazoanthus anguicomus, Parazoanthus catenularis, unclassified Parazoanthus, Parazoanthus juan-fernandezii, Parazoanthus cf. darwini MQ74b, Parazoanthus aff. swiftii TDS-2010, Parazoanthus aff. tunicans 'black', Parazoanthus aff. tunicans 'white', Parazoanthus aff. puertoricense JDR-2009, Parazoanthus aff. juan-fernandezii TDS-2022, Parazoanthus aff. juan-fernandezii TDS-2010
Ajugasterone C
Ajugasterone C is a steroid. Ajugasterone C is a natural product found in Zoanthus, Cyanotis arachnoidea, and other organisms with data available. D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
Crustecdysone
20-hydroxyecdysone is an ecdysteroid that is ecdysone substituted by a hydroxy group at position 20. It has a role as a plant metabolite and an animal metabolite. It is a 20-hydroxy steroid, an ecdysteroid, a 14alpha-hydroxy steroid, a 3beta-sterol, a 2beta-hydroxy steroid, a 22-hydroxy steroid, a 25-hydroxy steroid and a phytoecdysteroid. It is functionally related to an ecdysone. 20-Hydroxyecdysone is a natural product found in Asparagus filicinus, Trichobilharzia ocellata, and other organisms with data available. A steroid hormone that regulates the processes of MOLTING or ecdysis in insects. Ecdysterone is the 20-hydroxylated ECDYSONE. Crustecdysone is found in crustaceans. Crustecdysone is isolated from the marine crayfish Jasus lalandei in low yield (2 mg/ton D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones An ecdysteroid that is ecdysone substituted by a hydroxy group at position 20. COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Crustecdysone (20-Hydroxyecdysone) is a naturally occurring ecdysteroid hormone isolated from Serratula coronata which controls the ecdysis (moulting) and metamorphosis of arthropods, it inhibits caspase activity and induces autophagy via the 20E nuclear receptor complex, EcR-USP[1]. Crustecdysone exhibits regulatory or protective roles in the cardiovascular system[2]. Crustecdysone is an active metabolite of Ecdysone (HY-N0179)[3]. Crustecdysone (20-Hydroxyecdysone) is a naturally occurring ecdysteroid hormone isolated from Serratula coronata which controls the ecdysis (moulting) and metamorphosis of arthropods, it inhibits caspase activity and induces autophagy via the 20E nuclear receptor complex, EcR-USP[1]. Crustecdysone exhibits regulatory or protective roles in the cardiovascular system[2]. Crustecdysone is an active metabolite of Ecdysone (HY-N0179)[3].
Crustecdysone
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials SubCategory_DNP: : The sterols, Cholestanes Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Crustecdysone (20-Hydroxyecdysone) is a naturally occurring ecdysteroid hormone isolated from Serratula coronata which controls the ecdysis (moulting) and metamorphosis of arthropods, it inhibits caspase activity and induces autophagy via the 20E nuclear receptor complex, EcR-USP[1]. Crustecdysone exhibits regulatory or protective roles in the cardiovascular system[2]. Crustecdysone is an active metabolite of Ecdysone (HY-N0179)[3]. Crustecdysone (20-Hydroxyecdysone) is a naturally occurring ecdysteroid hormone isolated from Serratula coronata which controls the ecdysis (moulting) and metamorphosis of arthropods, it inhibits caspase activity and induces autophagy via the 20E nuclear receptor complex, EcR-USP[1]. Crustecdysone exhibits regulatory or protective roles in the cardiovascular system[2]. Crustecdysone is an active metabolite of Ecdysone (HY-N0179)[3].
n-{12-[(1-hydroxy-2-methylpropylidene)amino]-2-methyl-4,6,11,13-tetraazatricyclo[8.3.0.0³,⁷]trideca-1(10),3(7),5,11-tetraen-5-yl}benzenecarboximidic acid
C21H24N6O2 (392.19606439999995)
n-(3-{1-[2-(3-bromo-4-methoxyphenyl)ethenyl]-2-hydroxy-5-oxoimidazol-4-ylidene}propyl)guanidine
n-{3-[(4s)-1-[(1e)-2-(3-bromo-4-methoxyphenyl)ethenyl]-2-hydroxy-5-oxo-4h-imidazol-4-yl]propyl}guanidine
C16H20BrN5O3 (409.0749430000001)
2-methyl-4,6,11,13-tetraazatricyclo[8.3.0.0³,⁷]trideca-1,3(7),8,10-tetraene-5,12-diimine
n-(3-{2-hydroxy-1-[2-(4-methoxyphenyl)ethenyl]-5-oxoimidazol-4-ylidene}propyl)guanidine
C16H19N5O3 (329.14878239999996)
n-{12-[(1-hydroxy-3-methylbut-2-en-1-ylidene)amino]-2-methyl-4,6,11,13-tetraazatricyclo[8.3.0.0³,⁷]trideca-1(10),3(7),5,11-tetraen-5-yl}-3-methylbut-2-enimidic acid
12-imino-n,n,2-trimethyl-4,6,11,13-tetraazatricyclo[8.3.0.0³,⁷]trideca-1,3,5,7,9-pentaen-5-amine
n,n,9-trimethyl-12-(methylimino)-3,5,11,13-tetraazatricyclo[8.3.0.0²,⁶]trideca-1(13),2(6),4,7,9-pentaen-4-amine
12-imino-n,n,2,13-tetramethyl-4,6,11,13-tetraazatricyclo[8.3.0.0³,⁷]trideca-1,3,5,7,9-pentaen-5-amine
n-{3-[(4s)-2-hydroxy-1-[(1e)-2-(4-hydroxyphenyl)ethenyl]-5-oxo-4h-imidazol-4-yl]propyl}guanidine
C15H19N5O3 (317.14878239999996)
n-{12-imino-2-methyl-4,6,11,13-tetraazatricyclo[8.3.0.0³,⁷]trideca-1,3(7),8,10-tetraen-5-ylidene}methanamine
n-(3-{2-hydroxy-1-[(1e)-2-(4-hydroxyphenyl)ethenyl]-5-oxo-4h-imidazol-4-yl}propyl)guanidine
C15H19N5O3 (317.14878239999996)
n-(3-{2-hydroxy-1-[2-(4-hydroxyphenyl)ethenyl]-5-oxo-4h-imidazol-4-yl}propyl)guanidine
C15H19N5O3 (317.14878239999996)
n-[7-methyl-12-(methylimino)-3,5,11,13-tetraazatricyclo[8.3.0.0²,⁶]trideca-1(10),2,6,8-tetraen-4-ylidene]methanamine
n-[2-methyl-12-(methylimino)-4,6,11,13-tetraazatricyclo[8.3.0.0³,⁷]trideca-1(10),2,6,8-tetraen-5-ylidene]methanamine
n-(3-{1-[(1e)-2-(3-bromo-4-methoxyphenyl)ethenyl]-2-hydroxy-5-oxo-4h-imidazol-4-yl}propyl)guanidine
C16H20BrN5O3 (409.0749430000001)
n-{12-[(1-hydroxy-2-methylbutylidene)amino]-2-methyl-4,6,11,13-tetraazatricyclo[8.3.0.0³,⁷]trideca-1(10),3(7),5,11-tetraen-5-yl}benzenecarboximidic acid
(1s,3as,7r,8s,9ar,9br,11ar)-3a,7,8-trihydroxy-9a,11a-dimethyl-1-[(2r,3s)-2,3,6-trihydroxy-6-methylheptan-2-yl]-1h,2h,3h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-5-one
n-{12-imino-2-methyl-4,6,11,13-tetraazatricyclo[8.3.0.0³,⁷]trideca-1,3,7,9-tetraen-5-ylidene}methanamine
n-{3-[(4z)-2-hydroxy-1-[(1e)-2-(4-methoxyphenyl)ethenyl]-5-oxoimidazol-4-ylidene]propyl}guanidine
C16H19N5O3 (329.14878239999996)
n-{3-[(4z)-2-hydroxy-1-[(1e)-2-(4-hydroxyphenyl)ethenyl]-5-oxoimidazol-4-ylidene]propyl}guanidine
n-(3-{2-hydroxy-1-[2-(4-hydroxyphenyl)ethenyl]-5-oxoimidazol-4-ylidene}propyl)guanidine
n-{12-[(1-hydroxy-3-methylbut-2-en-1-ylidene)amino]-2-methyl-4,6,11,13-tetraazatricyclo[8.3.0.0³,⁷]trideca-1(10),3(7),5,11-tetraen-5-yl}benzenecarboximidic acid
C22H24N6O2 (404.19606439999995)
n-(3-{1-[2-(3-bromo-4-methoxyphenyl)ethenyl]-2-hydroxy-5-oxo-4h-imidazol-4-yl}propyl)guanidine
C16H20BrN5O3 (409.0749430000001)