NCBI Taxonomy: 36922
Diaporthe (ncbi_taxid: 36922)
found 500 associated metabolites at genus taxonomy rank level.
Ancestor: Diaporthaceae
Child Taxonomies: Diaporthe oxe, Diaporthe padi, Diaporthe caulivora, Diaporthe sojae, Diaporthe novem, Diaporthe rosae, Diaporthe rudis, Diaporthe oculi, Diaporthe citri, Diaporthe acuta, Diaporthe nigra, Diaporthe tersa, Diaporthe longicolla, Diaporthe baccae, Diaporthe ganjae, Diaporthe hordei, Diaporthe conica, Diaporthe bounty, Diaporthe viciae, Diaporthe scabra, Diaporthe schini, Diaporthe jinxiu, Diaporthe heveae, Diaporthe sennae, Diaporthe marina, Diaporthe minima, Diaporthe arctii, Diaporthe caryae, Diaporthe coryli, Diaporthe meliae, Diaporthe gulyae, Diaporthe kongii, Diaporthe hartii, Diaporthe moorei, Diaporthe neatei, Diaporthe rhoina, Diaporthe toxica, Diaporthe vexans, Diaporthe woodii, Diaporthe aceris, Diaporthe parvae, Diaporthe aseana, Diaporthe orixae, Diaporthe phaseolorum, Diaporthe crousii, Diaporthe ocoteae, Diaporthe pascoei, Diaporthe alangii, Diaporthe mayteni, Diaporthe carriae, Diaporthe gossiae, Diaporthe griceae, Diaporthe platzii, Diaporthe shawiae, Diaporthe araliae, Diaporthe searlei, Diaporthe ueckeri, Diaporthe arengae, Diaporthe batatas, Diaporthe detrusa, Diaporthe fibrosa, Diaporthe litchii, Diaporthe melonis, Diaporthe capsici, Diaporthe canthii, Diaporthe careyae, Diaporthe conorum, Diaporthe ambigua, Diaporthe machili, Diaporthe schimae, Diaporthe schoeni, Diaporthe acerina, Diaporthe carpini, Diaporthe nebulae, Diaporthe impulsa, Diaporthe viburni, Diaporthe scobina, Diaporthe tecomae, Diaporthe cf. oxe, Diaporthe perseae, Diaporthe tanakae, Diaporthe nomurai, Diaporthe spinosa, Diaporthe ovoidea, Diaporthe malorum, Diaporthe monetii, Diaporthe meridionalis, Diaporthe sterilis, Diaporthe eugeniae, Diaporthe kadsurae, Diaporthe beasleyi, Diaporthe asparagi, Diaporthe sophorae, Diaporthe moriniae, Diaporthe celtidis, Diaporthe taoicola, Diaporthe drenthii, Diaporthe stictica, Diaporthe sinensis, Diaporthe tuyouyou, Diaporthe decedens, Diaporthe musigena, Diaporthe amygdali, Diaporthe cuppatea, Diaporthe browniae, Diaporthe hazeniae, Diaporthe ampelina, Diaporthe tectonae, Diaporthe breyniae, Diaporthe cercidis, Diaporthe africana, Diaporthe afzeliae, Diaporthe bombacis, Diaporthe samaneae, Diaporthe rostrata, Diaporthe fusicola, Diaporthe osmanthi, Diaporthe compacta, Diaporthe bohemiae, Diaporthe pometiae, Diaporthe cichorii, Diaporthe italiana, Diaporthe goulteri, Diaporthe miriciae, Diaporthe crataegi, Diaporthe elaeagni, Diaporthe aquatica, Diaporthe velutina, Diaporthe cassines, Diaporthe undulata, Diaporthe zaobaisu, Diaporthe vawdreyi, Diaporthe limoniae, Diaporthe asheicola, Diaporthe ravennica, Diaporthe celticola, Diaporthe nothofagi, Diaporthe aspalathi, Diaporthe acerigena, Diaporthe gardeniae, Diaporthe cinnamomi, Diaporthe infecunda, Diaporthe neoarctii, Diaporthe howardiae, Diaporthe brideliae, Diaporthe x hybrida, Diaporthe pescicola, Diaporthe perjuncta, Diaporthe saccarata, Diaporthe delonicis, Diaporthe anacardii, Diaporthe destruens, Diaporthe oncostoma, Diaporthe pardalota, Diaporthe pustulata, Diaporthe foliicola, Diaporthe chinensis, Diaporthe lutescens, Diaporthe benedicti, Diaporthe rhusicola, Diaporthe siamensis, Diaporthe cf. sojae, Diaporthe hickoriae, Diaporthe stewartii, Diaporthe strumella, Diaporthe sennicola, Diaporthe acaciarum, Diaporthe helianthi, Diaporthe silvicola, Diaporthe virgiliae, Diaporthe vochysiae, Diaporthe guttulata, Diaporthe lenispora, Diaporthe nitschkei, Diaporthe apiculata, Diaporthe oraccinii, Diaporthe bauhiniae, Diaporthe hispaniae, Diaporthe hungariae, Diaporthe aitkeniae, Diaporthe viniferae, Diaporthe antonovae, Diaporthe acericola, Diaporthe kochmanii, Diaporthe berteroae, Diaporthe butterlyi, Diaporthe lonicerae, Diaporthe eucommiae, Diaporthe racemosae, Diaporthe heveicola, Diaporthe manihotia, Diaporthe angelicae, Diaporthe psoraleae, Diaporthe ilicicola, Diaporthe monospora, Diaporthe vangoghii, Diaporthe betulicola, Diaporthe phillipsii, Diaporthe rossmaniae, Diaporthe cissampeli, Diaporthe salicicola, Diaporthe aestuarium, Diaporthe annellsiae, Diaporthe humulicola, Diaporthe etinsideae, Diaporthe hunanensis, Diaporthe rauvolfiae, Diaporthe paranensis, Diaporthe lovelaceae, Diaporthe convolvuli, Diaporthe macadamiae, Diaporthe cucurbitae, Diaporthe hubeiensis, Diaporthe acaciigena, Diaporthe jazanensis, Diaporthe pterocarpi, Diaporthe longispora, Diaporthe foikelawen, Diaporthe patagonica, Diaporthe salinicola, Diaporthe tulliensis, Diaporthe litoricola, Diaporthe vangueriae, Diaporthe collariana, Diaporthe ovoicicola, Diaporthe limonicola, Diaporthe melitensis, Diaporthe henanensis, Diaporthe millettiae, Diaporthe cynaroidis, Diaporthe rhodomyrti, Diaporthe loropetali, Diaporthe krabiensis, Diaporthe torilicola, Diaporthe rumicicola, Diaporthe anhuiensis, Diaporthe beckhausii, Diaporthe actinidiae, Diaporthe sackstonii, Diaporthe serafiniae, Diaporthe acutispora, Diaporthe incompleta, Diaporthe juglandina, Diaporthe heliconiae, Diaporthe nelumbonis, Diaporthe columnaris, Diaporthe subclavata, Diaporthe ovalispora, Diaporthe sambucusii, Diaporthe perniciosa, Diaporthe cf. heveae, Diaporthe fulvicolor, Diaporthe fusiformis, Diaporthe corylicola, Diaporthe camporesii, Diaporthe fructicola, Diaporthe rizhaoensis, Diaporthe smilacicola, Diaporthe arezzoensis, Diaporthe beilharziae, Diaporthe unshiuensis, Diaporthe litchiicola, Diaporthe endophytica, Diaporthe inconspicua, Diaporthe fraxinicola, Diaporthe brumptoniae, Diaporthe mclennaniae, Diaporthe trevorrowii, Diaporthe citriasiana, Diaporthe australiana, Diaporthe lusitanicae, Diaporthe leucospermi, Diaporthe clematidina, Diaporthe cf. ueckeri, Diaporthe grandiflori, Diaporthe tectonigena, Diaporthe thunbergiae, Diaporthe crotalariae, Diaporthe minusculata, Diaporthe passiflorae, Diaporthe araucanorum, Diaporthe pseudoalnea, Diaporthe pimpinellae, Diaporthe irregularis, Diaporthe chimonanthi, Diaporthe ellipsoidea, Diaporthe pandanicola, Diaporthe penetriteum, Diaporthe macintoshii, Diaporthe masirevicii, Diaporthe middletonii, Diaporthe cinerascens, Diaporthe megalospora, Diaporthe rosiphthora, Diaporthe maytenicola, Diaporthe kyushuensis, Diaporthe woolworthii, Diaporthe foeniculina, Diaporthe hongheensis, Diaporthe pseudooculi, Diaporthe yunnanensis, Diaporthe biguttulata, Diaporthe schisandrae, Diaporthe chamaeropis, Diaporthe fujianensis, Diaporthe sapindicola, Diaporthe biconispora, Diaporthe pyracanthae, Diaporthe salsuginosa, Diaporthe campylandrae, Diaporthe ternstroemia, Diaporthe norfolkensis, Diaporthe toxicodendri, Diaporthe portugallica, Diaporthe cf. miriciae, Diaporthe spartinicola, Diaporthe mediterranea, Diaporthe melastomatis, Diaporthe obtusifoliae, Diaporthe cytosporella, Diaporthe brasiliensis, Diaporthe zaofenghuang, Diaporthe guangxiensis, Diaporthe phoenicicola, Diaporthe subordinaria, Diaporthe eucalyptorum, Diaporthe isoberliniae, unclassified Diaporthe, Diaporthe chromolaenae, Diaporthe albosinensis, Diaporthe ellipsospora, Diaporthe eucommiicola, Diaporthe ceratozamiae, Diaporthe shaanxiensis, Diaporthe huairouensis, Diaporthe pseudotsugae, Diaporthe guizhouensis, Diaporthe foeniculacea, Diaporthe juglandicola, Diaporthe diospyricola, Diaporthe juniperivora, Diaporthe tarchonanthi, Diaporthe nanjingensis, Diaporthe hsinchuensis, Diaporthe liquidambaris, Diaporthe hongkongensis, Diaporthe ukurunduensis, Diaporthe poincianellae, Diaporthe cameroonensis, Diaporthe fici-septicae, Diaporthe endocitricola, Diaporthe sclerotioides, Diaporthe cf. hungariae, Diaporthe subellipicola, Diaporthe discoidispora, Diaporthe donglingensis, Diaporthe forlicesenica, Diaporthe heterophyllae, Diaporthe caatingaensis, Diaporthe cf. acaciarum, Diaporthe garethjonesii, Diaporthe longipapillata, Diaporthe passifloricola, Diaporthe thunbergiicola, Diaporthe myracrodruonis, Diaporthe raonikayaporum, Diaporthe citrichinensis, Diaporthe guangdongensis, Diaporthe pterocarpicola, Diaporthe chongqingensis, Diaporthe parapterocarpi, Diaporthe globoostiolata, Diaporthe amaranthophila, Diaporthe cf. heveae C25, Diaporthe cf. heveae C22, Diaporthe chamaeropicola, Diaporthe phyllanthicola, Diaporthe huangshanensis, Diaporthe charlesworthii, Diaporthe xishuangbanica, Diaporthe multigutullata, Diaporthe australpacifica, Diaporthe pseudoanacardii, Diaporthe terebinthifolii, Diaporthe australafricana, Diaporthe heterostemmatis, Diaporthe aff. lithocarpi, Diaporthe cf. pseudooculi, Diaporthe constrictospora, Diaporthe caricae-papayae, Diaporthe chrysalidocarpi, Diaporthe angustiapiculata, Diaporthe pseudolongicolla, Diaporthe constancestoneae, Diaporthe pseudomangiferae, Diaporthe shennongjiaensis, Diaporthe cf. phoenicicola, Diaporthe subcylindrospora, Diaporthe cf. brasiliensis, Diaporthe elaeagni-glabrae, Diaporthe pseudoinconspicua, Diaporthe araliae-chinensis, Diaporthe tectonendophytica, Diaporthe leptostromiformis, Diaporthe cylindriformispora, Diaporthe camelliae-oleifera, Diaporthe pseudophoenicicola, Diaporthe camelliae-sinensis, Diaporthe aff. hongkongensis, Diaporthe psoraleae-pinnatae, Diaporthe cf. phaseolorum 92C, Diaporthe elizabethandersoniae, Diaporthe cf. pseudomangiferae, Diaporthe eres species complex, Diaporthe cf. heveae 1 RG-2013, Diaporthe cf. heveae 2 RG-2013, Diaporthe fraxini-angustifoliae, Diaporthe elizabethblackwelliae, Diaporthe cf. heveae 1 JCP-2019, Diaporthe podocarpi-macrophylli, Diaporthe cf. ampelina 'taxon 1', Diaporthe cf. mayteni UFMGCB4807, Diaporthe cf. phaseolorum UFMGCB 4602
Ergosterol
Ergosterol is a phytosterol consisting of ergostane having double bonds at the 5,6-, 7,8- and 22,23-positions as well as a 3beta-hydroxy group. It has a role as a fungal metabolite and a Saccharomyces cerevisiae metabolite. It is a 3beta-sterol, an ergostanoid, a 3beta-hydroxy-Delta(5)-steroid and a member of phytosterols. A steroid of interest both because its biosynthesis in FUNGI is a target of ANTIFUNGAL AGENTS, notably AZOLES, and because when it is present in SKIN of animals, ULTRAVIOLET RAYS break a bond to result in ERGOCALCIFEROL. Ergosterol is a natural product found in Gladiolus italicus, Ramaria formosa, and other organisms with data available. ergosterol is a metabolite found in or produced by Saccharomyces cerevisiae. A steroid occurring in FUNGI. Irradiation with ULTRAVIOLET RAYS results in formation of ERGOCALCIFEROL (vitamin D2). See also: Reishi (part of). Ergosterol, also known as provitamin D2, belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Thus, ergosterol is considered to be a sterol lipid molecule. Ergosterol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Ergosterol is the biological precursor to vitamin D2. It is turned into viosterol by ultraviolet light, and is then converted into ergocalciferol, which is a form of vitamin D. Ergosterol is a component of fungal cell membranes, serving the same function that cholesterol serves in animal cells. Ergosterol is not found in mammalian cell membranes. A phytosterol consisting of ergostane having double bonds at the 5,6-, 7,8- and 22,23-positions as well as a 3beta-hydroxy group. Ergosterol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=57-87-4 (retrieved 2024-07-12) (CAS RN: 57-87-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects. Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects.
Mesoridazine
Mesoridazine is only found in individuals that have used or taken this drug. It is a phenothiazine antipsychotic with effects similar to chlorpromazine. [PubChem]Based upon animal studies, mesoridazine, as with other phenothiazines, acts indirectly on reticular formation, whereby neuronal activity into reticular formation is reduced without affecting its intrinsic ability to activate the cerebral cortex. In addition, the phenothiazines exhibit at least part of their activities through depression of hypothalamic centers. Neurochemically, the phenothiazines are thought to exert their effects by a central adrenergic blocking action. N - Nervous system > N05 - Psycholeptics > N05A - Antipsychotics > N05AC - Phenothiazines with piperidine structure D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014150 - Antipsychotic Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D018377 - Neurotransmitter Agents > D015259 - Dopamine Agents > D018492 - Dopamine Antagonists D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants C78272 - Agent Affecting Nervous System > C66883 - Dopamine Antagonist C78272 - Agent Affecting Nervous System > C29710 - Antipsychotic Agent
Cinchonidine
Cinchonine is found in fruits. Cinchonine is an alkaloid from the leaves of Olea europaea Cinchonine is an alkaloidwith molecular formula C19H22N2O used in asymmetric synthesis in organic chemistry. It is a stereoisomer and pseudo-enantiomer of cinchonidine D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents [Raw Data] CB216_Cinchonine_pos_10eV_CB000075.txt [Raw Data] CB216_Cinchonine_pos_30eV_CB000075.txt [Raw Data] CB216_Cinchonine_pos_40eV_CB000075.txt [Raw Data] CB216_Cinchonine_pos_50eV_CB000075.txt [Raw Data] CB216_Cinchonine_pos_20eV_CB000075.txt Alkaloid from the leaves of Olea europaea Cinchonidine (α-Quinidine) is a cinchona alkaloid found in Cinchona officinalis and Gongronema latifolium. A building block used in asymmetric synthesis in organic chemistry. Weak inhibitor of serotonin transporter (SERT) with Kis of 330, 4.2, 36, 196, 15 μM for dSERT, hSERT, hSERT I172M, hSERT S438T, hSERT Y95F, respectively. Antimalarial activities[1]. Cinchonidine (α-Quinidine) is a cinchona alkaloid found in Cinchona officinalis and Gongronema latifolium. A building block used in asymmetric synthesis in organic chemistry. Weak inhibitor of serotonin transporter (SERT) with Kis of 330, 4.2, 36, 196, 15 μM for dSERT, hSERT, hSERT I172M, hSERT S438T, hSERT Y95F, respectively. Antimalarial activities[1]. Cinchonine is a natural compound present in Cinchona bark. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells[1]. Cinchonine is a natural compound present in Cinchona bark. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells[1].
Quinine
C20H24N2O2 (324.18376839999996)
Quinine is a cinchona alkaloid that is cinchonidine in which the hydrogen at the 6-position of the quinoline ring is substituted by methoxy. It has a role as an antimalarial, a muscle relaxant and a non-narcotic analgesic. It is a conjugate base of a quinine(1+). It derives from a hydride of an (8S)-cinchonan. An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood. Quinine is an Antimalarial. Quinine is a natural cinchona alkaloid that has been used for centuries in the prevention and therapy of malaria. Quinine is also used for idiopathic muscle cramps. Quinine therapy has been associated with rare instances of hypersensitivity reactions which can be accompanied by hepatitis and mild jaundice. Quinine is a natural product found in Cinchona calisaya, Cinchona officinalis, and other organisms with data available. Quinine is a quinidine alkaloid isolated from the bark of the cinchona tree. Quinine has many mechanisms of action, including reduction of oxygen intake and carbohydrate metabolism; disruption of DNA replication and transcription via DNA intercalation; and reduction of the excitability of muscle fibers via alteration of calcium distribution. This agent also inhibits the drug efflux pump P-glycoprotein which is overexpressed in multi-drug resistant tumors and may improve the efficacy of some antineoplastic agents. (NCI04) Quinine is an alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood. An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood. See also: Quinine Sulfate (active moiety of); Quinine salicylate (active moiety of); Quinine arsenite (active moiety of) ... View More ... Quinine is an alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood. [PubChem]. P - Antiparasitic products, insecticides and repellents > P01 - Antiprotozoals > P01B - Antimalarials > P01BC - Methanolquinolines A cinchona alkaloid that is cinchonidine in which the hydrogen at the 6-position of the quinoline ring is substituted by methoxy. D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents C254 - Anti-Infective Agent > C276 - Antiparasitic Agent > C277 - Antiprotozoal Agent D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D018373 - Peripheral Nervous System Agents > D009465 - Neuromuscular Agents D002491 - Central Nervous System Agents > D000700 - Analgesics It is used in tonics and bitter drinks [Raw Data] CB141_Quinine_pos_10eV_CB000051.txt [Raw Data] CB141_Quinine_pos_20eV_CB000051.txt [Raw Data] CB141_Quinine_pos_40eV_CB000051.txt [Raw Data] CB141_Quinine_pos_50eV_CB000051.txt [Raw Data] CB141_Quinine_pos_30eV_CB000051.txt Quinine is an alkaloid derived from the bark of the cinchona tree, acts as an anti-malaria agent. Quinine is a potassium channel inhibitor that inhibits WT mouse Slo3 (KCa5.1) channel currents evoked by voltage pulses to +100?mV with an IC50 of 169 μM[1][2]. Quinine is an alkaloid derived from the bark of the cinchona tree, acts as an anti-malaria agent. Quinine is a potassium channel inhibitor that inhibits WT mouse Slo3 (KCa5.1) channel currents evoked by voltage pulses to +100?mV with an IC50 of 169 μM[1][2].
ent-8(14),15-Pimaradiene
ent-8(14),15-Pimaradiene is found in fruits. ent-8(14),15-Pimaradiene is a constituent of Aralia racemosa (American spikenard). Constituent of Aralia racemosa (American spikenard). ent-8(14),15-Pimaradiene is found in fruits.
fusicocca-2,10(14)-diene
Phomopsin A
C36H45ClN6O12 (788.2783840000001)
D050258 - Mitosis Modulators > D050256 - Antimitotic Agents > D050257 - Tubulin Modulators Phomopsin A is a mycotoxin produced by Phomopsis leptostromiformi D000970 - Antineoplastic Agents > D050256 - Antimitotic Agents D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins
Quinidine
C20H24N2O2 (324.18376839999996)
Crystals or white powder. (NTP, 1992) Quinidine is a cinchona alkaloid consisting of cinchonine with the hydrogen at the 6-position of the quinoline ring substituted by methoxy. It has a role as an alpha-adrenergic antagonist, an antimalarial, an anti-arrhythmia drug, a sodium channel blocker, a muscarinic antagonist, a potassium channel blocker, a P450 inhibitor, an EC 1.14.13.181 (13-deoxydaunorubicin hydroxylase) inhibitor, an EC 3.6.3.44 (xenobiotic-transporting ATPase) inhibitor and a drug allergen. It derives from a hydride of a cinchonan. Quinidine is a D-isomer of [quinine] present in the bark of the Cinchona tree and similar plant species. This alkaloid was first described in 1848 and has a long history as an antiarrhythmic medication. Quinidine is considered the first antiarrhythmic drug (class Ia) and is moderately efficacious in the acute conversion of atrial fibrillation to normal sinus rhythm. It prolongs cellular action potential by blocking sodium and potassium currents. A phenomenon known as “quinidine syncope” was first described in the 1950s, characterized by syncopal attacks and ventricular fibrillation in patients treated with this drug. Due to its side effects and increased risk of mortality, the use of quinidine was reduced over the next few decades. However, it continues to be used in the treatment of Brugada syndrome, short QT syndrome and idiopathic ventricular fibrillation. Quinidine is an Antiarrhythmic and Cytochrome P450 2D6 Inhibitor. The mechanism of action of quinidine is as a Cytochrome P450 2D6 Inhibitor. Quinidine is a natural cinchona alkaloid which has potent antiarrhythmic activity and has been used for decades in the treatment of atrial and ventricular arrhythmias. Quinidine has been associated with fever, mild jaundice and clinically apparent liver injury in up to 2\\\\% of treated patients. Quinidex is a natural product found in Cinchona calisaya, Aspidosperma excelsum, and other organisms with data available. Quinidine is an alkaloid extracted from the bark of the Cinchona tree with class 1A antiarrhythmic and antimalarial effects. Quinidine stabilizes the neuronal membrane by binding to and inhibiting voltage-gated sodium channels, thereby inhibiting the sodium influx required for the initiation and conduction of impulses resulting in an increase of the threshold for excitation and decreased depolarization during phase 0 of the action potential. In addition, the effective refractory period (ERP), action potential duration (APD), and ERP/APD ratios are increased, resulting in decreased conduction velocity of nerve impulses. Quinidine exerts its antimalarial activity by acting primarily as an intra-erythrocytic schizonticide through association with the heme polymer (hemazoin) in the acidic food vacuole of the parasite thereby preventing further polymerization by heme polymerase enzyme. This results in accumulation of toxic heme and death of the parasite. An optical isomer of quinine, extracted from the bark of the CHINCHONA tree and similar plant species. This alkaloid dampens the excitability of cardiac and skeletal muscles by blocking sodium and potassium currents across cellular membranes. It prolongs cellular ACTION POTENTIALS, and decreases automaticity. Quinidine also blocks muscarinic and alpha-adrenergic neurotransmission. See also: Quinidine Gluconate (active moiety of); Quinidine Sulfate (active moiety of); Quinidine polygalacturonate (is active moiety of). An optical isomer of quinine, extracted from the bark of the Cinchona tree and similar plant species. This alkaloid dampens the excitability of cardiac and skeletal muscles by blocking sodium and potassium currents across cellular membranes. It prolongs cellular action potential, and decreases automaticity. Quinidine also blocks muscarinic and alpha-adrenergic neurotransmission. [PubChem] C - Cardiovascular system > C01 - Cardiac therapy > C01B - Antiarrhythmics, class i and iii > C01BA - Antiarrhythmics, class ia A cinchona alkaloid consisting of cinchonine with the hydrogen at the 6-position of the quinoline ring substituted by methoxy. D004791 - Enzyme Inhibitors > D065607 - Cytochrome P-450 Enzyme Inhibitors > D065690 - Cytochrome P-450 CYP2D6 Inhibitors D002317 - Cardiovascular Agents > D026941 - Sodium Channel Blockers > D061567 - Voltage-Gated Sodium Channel Blockers D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018680 - Cholinergic Antagonists D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents C254 - Anti-Infective Agent > C276 - Antiparasitic Agent > C277 - Antiprotozoal Agent COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D049990 - Membrane Transport Modulators C93038 - Cation Channel Blocker Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS [Raw Data] CBA33_Quinidine_pos_50eV_1-1_01_1622.txt [Raw Data] CBA33_Quinidine_pos_30eV_1-1_01_1620.txt [Raw Data] CBA33_Quinidine_pos_40eV_1-1_01_1621.txt [Raw Data] CBA33_Quinidine_pos_20eV_1-1_01_1619.txt [Raw Data] CBA33_Quinidine_pos_10eV_1-1_01_1616.txt Quinidine (15\\% dihydroquinidine) is an antiarrhythmic agent. Quinidine is a potent, orally active, selective cytochrome P450db inhibitor. Quinidine is also a K+ channel blocker with an IC50 of 19.9 μM, and can induce apoptosis. Quinidine can be used for malaria research[1][2][3][4]. Quinidine (15\% dihydroquinidine) is an antiarrhythmic agent. Quinidine is a potent, orally active, selective cytochrome P450db inhibitor. Quinidine is also a K+ channel blocker with an IC50 of 19.9 μM, and can induce apoptosis. Quinidine can be used for malaria research[1][2][3][4].
Cinchonidine
Cinchonidine is 8-epi-Cinchonan in which a hydrogen at position 9 is substituted by hydroxy (R configuration). A diasteroisomer of cinchonine, it occurs in the bark of most varieties of Cinchona shrubs, and is frequently used for directing chirality in asymmetric synthesis. It has a role as a metabolite. It is a cinchona alkaloid and an (8xi)-cinchonan-9-ol. It derives from a hydride of an (8S)-cinchonan. Cinchonidine is a natural product found in Cinchona calisaya, Cinchona officinalis, and other organisms with data available. 8-epi-Cinchonan in which a hydrogen at position 9 is substituted by hydroxy (R configuration). A diasteroisomer of cinchonine, it occurs in the bark of most varieties of Cinchona shrubs, and is frequently used for directing chirality in asymmetric synthesis. D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C87053 - Adrenergic Agonist C254 - Anti-Infective Agent > C276 - Antiparasitic Agent > C277 - Antiprotozoal Agent Origin: Plant; SubCategory_DNP: Alkaloids derived from anthranilic acid, Quinoline alkaloids Annotation level-1 [Raw Data] CBA34_Cinchonidine_pos_50eV_1-2_01_1626.txt [Raw Data] CBA34_Cinchonidine_pos_40eV_1-2_01_1625.txt [Raw Data] CBA34_Cinchonidine_pos_20eV_1-2_01_1623.txt [Raw Data] CBA34_Cinchonidine_pos_30eV_1-2_01_1624.txt [Raw Data] CBA34_Cinchonidine_pos_10eV_1-2_01_1617.txt Cinchonidine (α-Quinidine) is a cinchona alkaloid found in Cinchona officinalis and Gongronema latifolium. A building block used in asymmetric synthesis in organic chemistry. Weak inhibitor of serotonin transporter (SERT) with Kis of 330, 4.2, 36, 196, 15 μM for dSERT, hSERT, hSERT I172M, hSERT S438T, hSERT Y95F, respectively. Antimalarial activities[1]. Cinchonidine (α-Quinidine) is a cinchona alkaloid found in Cinchona officinalis and Gongronema latifolium. A building block used in asymmetric synthesis in organic chemistry. Weak inhibitor of serotonin transporter (SERT) with Kis of 330, 4.2, 36, 196, 15 μM for dSERT, hSERT, hSERT I172M, hSERT S438T, hSERT Y95F, respectively. Antimalarial activities[1]. Cinchonine is a natural compound present in Cinchona bark. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells[1]. Cinchonine is a natural compound present in Cinchona bark. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells[1].
Ergosterol peroxide
Ergosterol peroxide is found in fruits. Ergosterol peroxide is obtained from leaves of Ananas comosus (pineapple obtained from leaves of Ananas comosus (pineapple). Ergosterol peroxide is found in pineapple and fruits.
Phomopsin B
D050258 - Mitosis Modulators > D050256 - Antimitotic Agents > D050257 - Tubulin Modulators D000970 - Antineoplastic Agents > D050256 - Antimitotic Agents Phomopsin B is a mycotoxin from Phomopsis leptostromiformis. D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins
Cytochalasin Ppho
C30H41NO6 (511.29337260000005)
Cytochalasin Ppho is produced by Phomopsis sp Production by Phomopsis species
(R)-(6-Methoxy-4-quinolyl)-(5-vinylquinuclidin-2-yl)methanol
C20H24N2O2 (324.18376839999996)
Cytosporone B
Cytosporone B (Csn-B; Dothiorelone G) is a naturally occurring nuclear orphan receptor Nur77/NR4A1 agonist with an EC50 of 0.278 nM.
ent-Sandaracopimaradiene
Ent-sandaracopimaradiene, also known as (-)-8(14),15-isopimaradiene or (-)-isopimara-8(14),15-diene, is a member of the class of compounds known as diterpenoids. Diterpenoids are terpene compounds formed by four isoprene units. Thus, ent-sandaracopimaradiene is considered to be an isoprenoid lipid molecule. Ent-sandaracopimaradiene can be found in rice, which makes ent-sandaracopimaradiene a potential biomarker for the consumption of this food product.
CYTOSPORONE B
Cytosporone B (Csn-B; Dothiorelone G) is a naturally occurring nuclear orphan receptor Nur77/NR4A1 agonist with an EC50 of 0.278 nM.
4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoic acid
4-butoxy-6-(1-hydroxypentyl)-5,6-dihydro-2H-pyran-2-one
Phomopsin A
C36H45ClN6O12 (788.2783840000001)
D050258 - Mitosis Modulators > D050256 - Antimitotic Agents > D050257 - Tubulin Modulators D000970 - Antineoplastic Agents > D050256 - Antimitotic Agents D009676 - Noxae > D011042 - Poisons > D009183 - Mycotoxins
Cinchonine
Cinchonan in which a hydrogen at position 9 is substituted by hydroxy (S configuration). It occurs in the bark of most varieties of Cinchona shrubs, and is frequently used for directing chirality in asymmetric synthesis. D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents Origin: Plant; Formula(Parent): C19H22N2O; Bottle Name:Cinchonine; PRIME Parent Name:Cinchonine; PRIME in-house No.:V0325; SubCategory_DNP: Alkaloids derived from anthranilic acid, Quinoline alkaloids Annotation level-1 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.610 Acquisition and generation of the data is financially supported by the Max-Planck-Society IPB_RECORD: 2401; CONFIDENCE confident structure Cinchonine is a natural compound present in Cinchona bark. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells[1]. Cinchonine is a natural compound present in Cinchona bark. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells[1].
Ergosterol
Indicator of fungal contamination, especies in cereals. Occurs in yeast and fungi. The main fungal steroidand is also found in small amts. in higher plant prods., e.g. palm oil [DFC]. D018977 - Micronutrients > D014815 - Vitamins > D000072664 - Provitamins Disclaimer: While authors make an effort to ensure that the content of this record is accurate, the authors make no representations or warranties in relation to the accuracy or completeness of the record. This record do not reflect any viewpoints of the affiliation and organization to which the authors belong. Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects. Ergosterol is the primary sterol found in fungi, with antioxidative, anti-proliferative, and anti-inflammatory effects.
Quinine
C20H24N2O2 (324.18376839999996)
CONFIDENCE standard compound; INTERNAL_ID 270; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5966; ORIGINAL_PRECURSOR_SCAN_NO 5964 P - Antiparasitic products, insecticides and repellents > P01 - Antiprotozoals > P01B - Antimalarials > P01BC - Methanolquinolines D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents C254 - Anti-Infective Agent > C276 - Antiparasitic Agent > C277 - Antiprotozoal Agent D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D018373 - Peripheral Nervous System Agents > D009465 - Neuromuscular Agents D002491 - Central Nervous System Agents > D000700 - Analgesics CONFIDENCE standard compound; INTERNAL_ID 270; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5977; ORIGINAL_PRECURSOR_SCAN_NO 5975 CONFIDENCE standard compound; INTERNAL_ID 270; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5998; ORIGINAL_PRECURSOR_SCAN_NO 5996 CONFIDENCE standard compound; INTERNAL_ID 270; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 5996; ORIGINAL_PRECURSOR_SCAN_NO 5994 CONFIDENCE standard compound; INTERNAL_ID 270; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6003; ORIGINAL_PRECURSOR_SCAN_NO 6001 CONFIDENCE standard compound; INTERNAL_ID 270; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 6016; ORIGINAL_PRECURSOR_SCAN_NO 6013 Origin: Plant; SubCategory_DNP: Monoterpenoid indole alkaloids, Cinchona alkaloids, Indole alkaloids relative retention time with respect to 9-anthracene Carboxylic Acid is 0.728 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.722 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.721 Quinine is an alkaloid derived from the bark of the cinchona tree, acts as an anti-malaria agent. Quinine is a potassium channel inhibitor that inhibits WT mouse Slo3 (KCa5.1) channel currents evoked by voltage pulses to +100?mV with an IC50 of 169 μM[1][2]. Quinine is an alkaloid derived from the bark of the cinchona tree, acts as an anti-malaria agent. Quinine is a potassium channel inhibitor that inhibits WT mouse Slo3 (KCa5.1) channel currents evoked by voltage pulses to +100?mV with an IC50 of 169 μM[1][2].
mesoridazine
N - Nervous system > N05 - Psycholeptics > N05A - Antipsychotics > N05AC - Phenothiazines with piperidine structure D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014150 - Antipsychotic Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents D018377 - Neurotransmitter Agents > D015259 - Dopamine Agents > D018492 - Dopamine Antagonists D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants C78272 - Agent Affecting Nervous System > C66883 - Dopamine Antagonist C78272 - Agent Affecting Nervous System > C29710 - Antipsychotic Agent
Quinidine
C20H24N2O2 (324.18376839999996)
Annotation level-1 Quinidine (15\\% dihydroquinidine) is an antiarrhythmic agent. Quinidine is a potent, orally active, selective cytochrome P450db inhibitor. Quinidine is also a K+ channel blocker with an IC50 of 19.9 μM, and can induce apoptosis. Quinidine can be used for malaria research[1][2][3][4]. Quinidine (15\% dihydroquinidine) is an antiarrhythmic agent. Quinidine is a potent, orally active, selective cytochrome P450db inhibitor. Quinidine is also a K+ channel blocker with an IC50 of 19.9 μM, and can induce apoptosis. Quinidine can be used for malaria research[1][2][3][4].
ent-8(14),15-Pimaradiene
3-(3,5-dimethylhepta-1,3-dien-1-yl)-8-hydroxy-3,4-dihydro-2-benzopyran-1-one
6-[(3s)-3-hydroxybutan-2-yl]-4-methoxy-5-methylpyran-2-one
[(1r,7ar)-1-[(1s)-1-[(2r,3s,4s)-3-hydroxy-4,5,5-trimethyloxolan-2-yl]ethyl]-7a-methyl-5-oxo-2,3,6,7-tetrahydro-1h-inden-4-yl]acetic acid
3-[3-(2-hydroxypropan-2-yl)-7-methyl-2,3-dihydro-1,4-benzodioxin-5-yl]-3-methoxy-4-(3-methylbut-2-en-1-yl)isoindole-1,7-diol
(1r,2s,13r,14s,15r,16r,17s,28s)-8,10,14,23,25,28-hexahydroxy-6,21-dimethoxyoctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,10,19,21,23,25-octaene-3,12,18,27-tetrone
6-(3-hydroxybutan-2-yl)-4-methoxy-5-methylpyran-2-one
5,7-dihydroxy-1-(1-hydroxyethyl)naphtho[2,3-c]furan-4,9-dione
(4as,7r,8ar)-7-hydroxy-4-(hydroxymethyl)-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-1h-naphthalen-2-one
(2s,3s,4s,5s,6r)-2-{[(1e,3r,4s,8r,9r,10r,11s,14s)-4,9-dihydroxy-6-[(2s)-1-hydroxypropan-2-yl]-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxane-3,4,5-triol
(2r)-2,3-dihydroxypropyl 7-methoxy-6-methyl-1-oxo-3h-2-benzofuran-4-carboxylate
8,10,14,23,25,28-hexahydroxy-6,21-dimethoxyoctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,10,19,21,23,25-octaene-3,12,18,27-tetrone
(6r,6ar,9s,9as)-9-acetyl-5-chloro-3-[(1e,3e,5s)-3,5-dimethylhepta-1,3-dien-1-yl]-6-methoxy-6a-methyl-6h,9h,9ah-furo[2,3-h]isochromen-8-one
C24H29ClO5 (432.17034140000004)
(1r,4s,9s,10s,13r)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane
2,5-dihydroxy-6-methoxy-3-(7-methyl-3-methylideneoct-6-en-1-yn-1-yl)cyclohex-3-en-1-one
(1r,4s,9s,10s,13s)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane
(2s,3r)-5-hydroxy-2-(2-hydroxypropan-2-yl)-3-[(3s)-3-(2-hydroxypropan-2-yl)-7-methyl-2,3-dihydro-1,4-benzodioxin-5-yl]-2,3-dihydro-1h-indene-4-carbaldehyde
(1s,4s,9s,10s,13s)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane
3,3'-bis[3-(2-hydroxypropan-2-yl)-7-methyl-2,3-dihydro-1,4-benzodioxin-5-yl]-4,4'-bis(3-methylbut-2-en-1-yl)-[1,1'-biisoindolylidene]-7,7'-diol
C50H54N2O8 (810.3879964000001)
methyl 8-hydroxy-9-oxo-6-(2-oxopropyl)xanthene-1-carboxylate
(1r,2s,13r,14s,15r,16r,17s,28s)-7,10,14,23,25,28-hexahydroxy-5,21-dimethoxyoctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,10,19,21,23,25-octaene-3,12,18,27-tetrone
4,6-dihydroxy-5-methoxy-2-(7-methyl-3-methylideneoct-6-en-1-yn-1-yl)cyclohex-2-en-1-one
2-[4,9,14-trihydroxy-14-(methoxymethyl)-3,10-dimethyl-8-[(3,4,5-trihydroxy-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxan-2-yl)oxy]tricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-6-yl]propyl acetate
2-[3-(2,3-dihydroxy-3-methylbutoxy)-2-hydroxy-5-methylbenzoyl]-6-hydroxy-3-(3-methylbut-2-en-1-yl)benzaldehyde
(2e)-2-[(e)-[(2e)-2-({[(2s)-1-[(3r,4s,7s,10s,11s)-14-chloro-3-ethyl-6,9,11,15-tetrahydroxy-3-methyl-10-(methylamino)-7-(prop-1-en-2-yl)-2-oxa-5,8-diazabicyclo[10.3.1]hexadeca-1(16),5,8,12,14-pentaene-4-carbonyl]-2,5-dihydropyrrol-2-yl](hydroxy)methylidene}amino)-1-hydroxy-3-methylpent-2-en-1-ylidene]amino]but-2-enedioic acid
C36H45ClN6O12 (788.2783840000001)
(4as,7s,10as)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene
2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene
(1s,3s,4s,4ar,9as)-1,4,8,9a-tetrahydroxy-4a-(hydroxymethyl)-3-methyl-2,3,4,10-tetrahydro-1h-anthracen-9-one
(1s,4s,9s,10s,13r)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane
(2s)-2-[(2e)-but-2-en-2-yl]-3-methyl-8-phenyl-2h-pyrano[3,2-c]pyridin-5-ol
1-{4-[3-(hydroxymethyl)-5-methoxyphenoxy]-2-methoxy-6-methylphenyl}-3-methylbut-3-en-2-one
(3s,6r,7r)-6,10-dihydroxy-2-oxatricyclo[7.4.0.0³,⁷]trideca-1(13),9,11-trien-8-one
(1s,2r,5r,6r,9r,10r,13s,15s)-5-[(2r,3e,5s)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol
6-hydroxy-2-[3-(2-hydroxypropan-2-yl)-7-methyl-2,3-dihydro-1,4-benzodioxine-5-carbonyl]-3-(3-methylbut-2-en-1-yl)benzoic acid
(1s,3r,5r,9r,10r)-5-ethenyl-2,3,9,10-tetrahydroxy-5,11,11-trimethyl-16-oxatetracyclo[7.5.2.0¹,¹⁰.0²,⁷]hexadec-6-en-8-one
(2s,3r,6s)-6-(hydroxymethyl)-3,4-dimethyl-9-phenyl-7-oxa-11-azatricyclo[6.4.0.0²,⁶]dodeca-1(12),4,8,10-tetraen-12-ol
C19H19NO3 (309.13648639999997)
1-{4-[3-hydroxy-5-(hydroxymethyl)phenoxy]-2-methoxy-6-methylphenyl}-3-methylbut-3-en-2-one
[(2s,3r)-2-[(2s)-5-hydroxy-2-(hydroxymethyl)-4-oxo-3h-1-benzopyran-2-yl]-5-oxooxolan-3-yl]methyl acetate
2-{[(2-methylbut-3-en-2-yl)oxy]methyl}-6-{[4,9,14-trihydroxy-6-isopropyl-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}oxane-3,4,5-triol
(2s)-5-hydroxy-2-[(s)-hydroxy[(3r)-5-oxooxolan-3-yl]methyl]-2-(hydroxymethyl)-3h-1-benzopyran-4-one
(2s)-2-[(3r,4s,8r,9r,10r,11s,14s)-8-{[(2s,3s,4r,5s,6s)-5-(acetyloxy)-3,4-dihydroxy-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxan-2-yl]oxy}-4,9-dihydroxy-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-6-yl]propyl acetate
(3r)-3-[(3s)-3-(2-hydroxypropan-2-yl)-7-methyl-2,3-dihydro-1,4-benzodioxin-5-yl]-4-(3-methylbut-2-en-1-yl)-3h-isoindole-1,7-diol
C25H29NO5 (423.20456240000004)
(1as,3r,4r,4ar,8ar)-3-hydroxy-3,4a,8,8-tetramethyl-hexahydronaphtho[1,8a-b]oxirene-4-carboxylic acid
(1s,4s,9s,10s,13r,14r)-5,5,9,14-tetramethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-14-ol
(2s)-2-[(3r,4s,8r,9r,10r,11s,14s)-4-(acetyloxy)-8-{[(2s,3s,4r,5s,6r)-5-(acetyloxy)-3,4-dihydroxy-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxan-2-yl]oxy}-9-hydroxy-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-6-yl]propyl acetate
2-({2-[({1-[14-chloro-10-(dimethylamino)-3-ethyl-6,9,11,15-tetrahydroxy-3-methyl-7-(prop-1-en-2-yl)-2-oxa-5,8-diazabicyclo[10.3.1]hexadeca-1(16),5,8,12,14-pentaene-4-carbonyl]-2,5-dihydropyrrol-2-yl}(hydroxy)methylidene)amino]-1-hydroxy-3-methylpent-2-en-1-ylidene}amino)but-2-enedioic acid
C37H47ClN6O12 (802.2940332000001)
methyl 4,5-dihydroxy-6-(2-hydroxyethyl)-8-methoxy-9-oxoxanthene-1-carboxylate
methyl 7-methoxy-4-oxo-3-[(1e)-3-oxobut-1-en-1-yl]chromene-5-carboxylate
8-hydroxy-3,5-dimethyl-3,4-dihydro-2-benzopyran-1-one
(2s)-2-[(1e,3r,4s,8r,9r,10r,11s,14s)-8-{[(2s,3r,4r,5r,6r)-4-(acetyloxy)-3,5-dihydroxy-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxan-2-yl]oxy}-4,9-dihydroxy-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-6-yl]propyl acetate
methyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate
2-{[4,9-dihydroxy-14-(hydroxymethyl)-6-isopropyl-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxane-3,4,5-triol
(2r,3s,6r)-4-(hydroxymethyl)-3,6-dimethyl-9-phenyl-7-oxa-11-azatricyclo[6.4.0.0²,⁶]dodeca-1(12),4,8,10-tetraen-12-ol
C19H19NO3 (309.13648639999997)
4-(hydroxymethyl)-7-methoxy-6-methyl-3h-2-benzofuran-1-one
ethyl 2-{2-[6-(acetyloxy)octanoyl]-3,5-dihydroxyphenyl}acetate
4,5-dihydroxy-2-[hydroxy(phenyl)methyl]-4-(1,3,4-trimethyl-2-oxocyclopent-3-en-1-yl)-2h-pyrrol-3-one
C19H21NO5 (343.14196560000005)
5-chloro-9-(1,1-dimethoxyethyl)-3-(3,5-dimethylhepta-1,3-dien-1-yl)-6a-methylfuro[2,3-h]isochromene-6,8-dione
C25H29ClO6 (460.16525640000003)
(3s)-7-hydroxy-3-[(3s)-3-(2-hydroxypropan-2-yl)-7-methyl-2,3-dihydro-1,4-benzodioxin-5-yl]-4-(3-methylbut-2-en-1-yl)-3h-2-benzofuran-1-one
7,9-dihydroxy-7-[(4-hydroxyphenyl)methyl]-2,4,5,16,18,20-hexamethyl-8-azapentacyclo[10.8.0.0²,¹⁰.0⁶,¹⁰.0¹³,¹⁸]icosa-3,8,19-trien-11-one
C32H41NO4 (503.30354260000007)
(3ar)-1-isopropyl-3a,6,10-trimethyl-2h,3h,4h,7h,8h,11h,12h-cyclopenta[11]annulene
(4,5,7-trihydroxy-9,10-dioxoanthracen-2-yl)methyl acetate
(2r,3s,4s,5r,6s)-2-{[(2-methylbut-3-en-2-yl)oxy]methyl}-6-{[(1e,3r,4s,8r,9r,10r,11s,14r)-4,9,14-trihydroxy-6-isopropyl-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}oxane-3,4,5-triol
(2s,3r,4s,5s,6r)-2-{[(1e,3r,8r,9r,10r,11s,14s)-9,14-dihydroxy-14-(hydroxymethyl)-6-isopropyl-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
(2r,4as,8as)-4-(hydroxymethyl)-3,4a,8,8-tetramethyl-1,2,5,6,7,8a-hexahydronaphthalen-2-ol
1-[2-methoxy-4-(3-methoxy-5-methylphenoxy)-6-methylphenyl]-3-methylbut-3-en-2-one
(2r)-2-[(2e)-but-2-en-2-yl]-3-methyl-8-phenyl-2h-pyrano[3,2-c]pyridin-5-ol
(2s,3s,4s,5s,6r)-2-{[(3r,4s,8r,9r,10r,11s,14s)-4,9-dihydroxy-6-[(2s)-1-hydroxypropan-2-yl]-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxane-3,4,5-triol
1,3,4-trihydroxy-8-methoxy-5-(1,3,4-trihydroxybutan-2-yl)xanthen-9-one
(2s)-5-hydroxy-2-(hydroxymethyl)-2-[(2s,3r)-3-(hydroxymethyl)-5-oxooxolan-2-yl]-3h-1-benzopyran-4-one
(5s,6r)-2-{[(1e,3r,4s,8r,9r,10r,11s,14s)-4,9-dihydroxy-14-(hydroxymethyl)-6-isopropyl-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
9-acetyl-5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-6-hydroxy-6a-methyl-6h,9h,9ah-furo[2,3-h]isochromen-8-one
C23H27ClO5 (418.15469220000006)
(4as,7r,10as)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene
6,10-dihydroxy-2-oxatricyclo[7.4.0.0³,⁷]trideca-1(13),9,11-trien-8-one
2-hydroxy-2,5,5,8a-tetramethyl-hexahydro-1h-naphthalene-1-carboxylic acid
1-(5,6-dimethylhept-3-en-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
(2r,3s,6r)-9-(4-hydroxyphenyl)-3,4,6-trimethyl-7-oxa-11-azatricyclo[6.4.0.0²,⁶]dodeca-1(12),4,8,10-tetraen-12-ol
C19H19NO3 (309.13648639999997)
methyl 6-hydroxy-2-[3-(2-hydroxypropan-2-yl)-7-methyl-2,3-dihydro-1,4-benzodioxine-5-carbonyl]-3-(3-methylbut-2-en-1-yl)benzoate
(2e,4e,6s,7s)-8-{[(1r,2r,7s,8ar)-1,8a-dimethyl-6-oxo-7-(prop-1-en-2-yl)-1,2,3,4,7,8-hexahydronaphthalen-2-yl]oxy}-6-hydroxy-7-methyl-8-oxoocta-2,4-dienoic acid
butyl 4-{5-[(1r)-1-hydroxyethyl]furan-2-yl}-4-oxobutanoate
2-{[4,9-dihydroxy-6-isopropyl-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxane-3,4,5-triol
3-[(1,2-dihydroxy-3-methylbutylidene)amino]prop-2-enoic acid
(1s,2r,5s)-5-(hydroxymethyl)-2-isopropylcyclohexan-1-ol
(1s,2r,4s,5r)-2-isopropyl-5-methylcyclohexane-1,4-diol
(1s,2s,9s,10r,14r)-2,6,11,11,14-pentamethyltetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene
2-{3-[(2r)-2,3-dihydroxy-3-methylbutoxy]-2-hydroxy-5-methylbenzoyl}-6-hydroxy-3-(3-methylbut-2-en-1-yl)benzaldehyde
7-hydroxy-4-(hydroxymethyl)-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-1h-naphthalen-2-one
(2z,3e)-2-ethylidene-4-[(1s)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]but-3-enoic acid
(1s,4r,5r,9s,10s,11r,13s,14r)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-11,14-diol
(2r,3s,6r)-6-(hydroxymethyl)-3,4-dimethyl-9-phenyl-7-oxa-11-azatricyclo[6.4.0.0²,⁶]dodeca-1(12),4,8,10-tetraen-12-ol
C19H19NO3 (309.13648639999997)
(2r,3s,6r)-3,4,6-trimethyl-11-phenyl-7-oxa-9-azatricyclo[6.4.0.0²,⁶]dodeca-1(12),4,8,10-tetraen-12-ol
(1s,2s,5s,6r,9s,10r,15s)-5-(5,6-dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol
(3ar,12ar)-3a,6,10-trimethyl-1-(propan-2-ylidene)-2h,3h,4h,7h,8h,11h,12h,12ah-cyclopenta[11]annulene
(6s)-4-butoxy-6-[(1s)-1-hydroxypentyl]-5,6-dihydropyran-2-one
(6ar,8s,9s,9as)-9-acetyl-5-chloro-3-[(1e,3e,5s)-3,5-dimethylhepta-1,3-dien-1-yl]-8-methoxy-6a,8-dimethyl-9h,9ah-furo[2,3-h]isochromen-6-one
(6z)-5-hydroxy-3-(1-hydroxyethyl)-6-isopropyl-2,3-dihydro-1,4-oxazocin-8-one
methyl 4,8-dihydroxy-9-oxo-6-(2-oxopropyl)xanthene-3-carboxylate
1-{4-[3-(hydroxymethyl)-5-methoxyphenoxy]-2-methoxy-6-methylphenyl}ethanone
(1r,2e,4s,5r)-4,5-dihydroxy-1-[(2r)-5-oxooxolan-2-yl]hex-2-en-1-yl (2e)-2-methylbut-2-enoate
5-ethenyl-5,11,11-trimethyl-16-oxatetracyclo[7.5.2.0¹,¹⁰.0²,⁷]hexadec-6-ene-2,3,8,9,10-pentol
(5s,6r)-2-{[(3r,4s,8r,9r,10r,11s,14s)-4,9-dihydroxy-6-isopropyl-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
(6ar,8r,9s,9as)-9-acetyl-5-chloro-3-[(1e,3e,5s)-3,5-dimethylhepta-1,3-dien-1-yl]-8-methoxy-6a,8-dimethyl-9h,9ah-furo[2,3-h]isochromen-6-one
7-hydroxy-8-(hydroxymethyl)-4,4,7,8a-tetramethyl-hexahydronaphthalen-2-one
methyl 6,11,11,14-tetramethyl-7-oxotetracyclo[7.6.0.0¹,⁵.0¹⁰,¹⁴]pentadec-5-ene-2-carboxylate
(1r,3ar,7s,9ar,9bs,11ar)-1-[(2r,3e,5s)-5,6-dimethylhept-3-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol
(1s,2r,3s,4r)-4-isopropyl-1-methylcyclohexane-1,2,3-triol
(2s,3r,4s,5s,6r)-2-{[(1e,3r,4s,8r,9r,10r,11s,14s)-4,9-dihydroxy-6-isopropyl-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxane-3,4,5-triol
6,8a-dihydroxy-5-(hydroxymethyl)-1,1,4a,6-tetramethyl-tetrahydro-3h-naphthalen-2-one
5-ethenyl-2,3,9,10-tetrahydroxy-5,11,11-trimethyl-16-oxatetracyclo[7.5.2.0¹,¹⁰.0²,⁷]hexadec-6-en-8-one
(2r,3r)-5-hydroxy-2-(2-hydroxypropan-2-yl)-3-[(3s)-3-(2-hydroxypropan-2-yl)-7-methyl-2,3-dihydro-1,4-benzodioxin-5-yl]-2,3-dihydro-1h-indene-4-carbaldehyde
(2s)-2-[(3r,4s,8r,9r,10r,11s,14s)-4-(acetyloxy)-8-{[(2s,3r,4s,5r,6r)-4-(acetyloxy)-3,5-dihydroxy-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxan-2-yl]oxy}-9-hydroxy-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-6-yl]propyl acetate
(2e)-2-[(e)-[(2e)-2-({[(2s)-1-[(3r,4s,7s,10s,11s)-14-chloro-10-(dimethylamino)-3-ethyl-6,9,11,15-tetrahydroxy-3-methyl-7-(prop-1-en-2-yl)-2-oxa-5,8-diazabicyclo[10.3.1]hexadeca-1(16),5,8,12,14-pentaene-4-carbonyl]-2,5-dihydropyrrol-2-yl](hydroxy)methylidene}amino)-1-hydroxy-3-methylpent-2-en-1-ylidene]amino]but-2-enedioic acid
C37H47ClN6O12 (802.2940332000001)
9-acetyl-5-chloro-3-(3,5-dimethylhepta-1,3-dien-1-yl)-8-methoxy-6a,8-dimethyl-9h,9ah-furo[2,3-h]isochromen-6-one
7-ethenyl-1,1,4a,7-tetramethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene
12-isopropyl-1,4,8-trimethyltricyclo[9.3.0.0³,⁷]tetradeca-3,11-diene
8-{[1,8a-dimethyl-6-oxo-7-(prop-1-en-2-yl)-1,2,3,4,7,8-hexahydronaphthalen-2-yl]oxy}-6-hydroxy-7-methyl-8-oxoocta-2,4-dienoic acid
3-(4-methoxy-5-methyl-6-oxopyran-2-yl)-2-methylprop-2-enoic acid
(3s)-3-[(1e,3e,5s)-3,5-dimethylhepta-1,3-dien-1-yl]-8-hydroxy-3,4-dihydro-2-benzopyran-1-one
8-hydroxy-4-(2-hydroxyethyl)-1,3-dimethoxyxanthen-9-one
3,3'-bis[(3s)-3-(2-hydroxypropan-2-yl)-7-methyl-2,3-dihydro-1,4-benzodioxin-5-yl]-4,4'-bis(3-methylbut-2-en-1-yl)-[1,1'-biisoindolylidene]-7,7'-diol
C50H54N2O8 (810.3879964000001)
6-hydroxy-4-(hydroxymethyl)-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-1h-naphthalen-2-one
(2s)-2-[(1e,3r,4s,8r,9r,10r,11s,14s)-4-(acetyloxy)-8-{[(2s,3s,4r,5s,6r)-5-(acetyloxy)-3,4-dihydroxy-6-{[(2-methylbut-3-en-2-yl)oxy]methyl}oxan-2-yl]oxy}-9-hydroxy-14-(methoxymethyl)-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-6-yl]propyl acetate
(3s,3ar,4s,6s,6ar,10s,12s,15r,15ar)-3-[(4-hydroxyphenyl)methyl]-4,10,12-trimethyl-5-methylidene-3h,3ah,4h,6h,6ah,9h,10h,11h,12h,15h-cycloundeca[d]isoindole-1,6,15-triol
C28H37NO4 (451.27224420000005)
4-hydroxy-6,15,15-trimethyl-2,10,14-trioxatetracyclo[10.8.0.0³,⁸.0¹³,¹⁸]icosa-1(12),3,5,7,13(18),16,19-heptaen-11-one
(1s,3s,4ar,9ar)-1,8,9a-trihydroxy-4a-(hydroxymethyl)-3-methyl-2,3-dihydro-1h-xanthene-4,9-dione
(5s,6r)-2-{[(1e,3r,8r,9r,10r,11s,14r)-9-hydroxy-14-(hydroxymethyl)-6-isopropyl-3,10-dimethyltricyclo[9.3.0.0³,⁷]tetradeca-1,6-dien-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
3-hydroxy-7-methoxy-6-methyl-1-oxo-3h-2-benzofuran-4-carboxylic acid
(3s,3ar,4s,6s,6ar,10s,12s,15r,15ar)-3-[(3-hydroxyphenyl)methyl]-4,10,12-trimethyl-5-methylidene-3h,3ah,4h,6h,6ah,9h,10h,11h,12h,15h-cycloundeca[d]isoindole-1,6,15-triol
C28H37NO4 (451.27224420000005)