On the public citation graph

Jatrophone, a novel macrocyclic diterpenoid tumor inhibitor from Jatropha gossypiifolia

https://doi.org/10.1021/ja00717a066
0 signed · 142 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4142190openalex-extracted
inferred← citeshttps://doi.org/10.1002/(sici)1099-1573(199608)10:5<375::aid-ptr847>3.0.co;2-#openalex-snapshot
Antiprotozoal activity of Jatrogrossidione from Jatropha grossidentata and Jatrophone from Jatropha isabellii
inferred← citeshttps://doi.org/10.1002/(sici)1099-1573(199912)13:8<660::aid-ptr528>3.0.co;2-xopenalex-snapshot
Molluscicidal activity of the diterpenoids jatrophone and jatropholones A and B isolated fromJatropha elliptica (Pohl) Muell. Arg.
inferred← citeshttps://doi.org/10.1002/(sici)1099-1573(200002)14:1<60::aid-ptr597>3.0.co;2-bopenalex-snapshot
The antimicrobial activity of roots ofJatropha podagrica (Hook)
inferred← citeshttps://doi.org/10.1002/9783527831883.ch18openalex-snapshot
Complex Natural Product Total Syntheses Facilitated by Palladium‐Catalyzed Carbonylative Cyclizations
inferred← citeshttps://doi.org/10.1002/ajoc.201500398openalex-snapshot
A General Strategy for Synthesis of Heterocyclic Hemiketal‐Containing α,β‐Unsaturated Ketones from Ynediones
inferred← citeshttps://doi.org/10.1002/ardp.19713042402openalex-snapshot
Cancerostatisch wirksame Inhaltsstoffe höherer Pflanzen
inferred← citeshttps://doi.org/10.1002/cbdv.200700461openalex-snapshot
Chemical Constituents of the Plants from Genus Jatropha
inferred← citeshttps://doi.org/10.1002/cbdv.202500956openalex-snapshot
Bioactive Rosane and Podocarpane Diterpenoids From the Whole Plant of Jatropha curcas L.
inferred← citeshttps://doi.org/10.1002/chem.202401999openalex-snapshot
Multicomponent Synthesis of 3(2H)‐Furanones Initiated by Copper(II)‐Catalyzed Alkyne‐Carbonyl Cross Metathesis
inferred← citeshttps://doi.org/10.1002/chin.197042417openalex-snapshot
ChemInform Abstract: TUMOR‐INHIBITOREN 59. MITT. JATROPHON, EIN NEUER TUMOR‐INHIBITOR MIT MAKROCYCLISCHER DITERPENOID‐STRUKTUR AUS JATROPHA GOSSYPIIFOLIA
inferred← citeshttps://doi.org/10.1002/chin.197903187openalex-snapshot
ChemInform Abstract: CONJUGATED ADDITION TO 2,2‐DIMETHYL‐3(2H)‐FURANONE‐ SUPPORT FOR THE BALDWIN RULES FOR RING CLOSURE
inferred← citeshttps://doi.org/10.1002/ejoc.201300148openalex-snapshot
Towards the Total Synthesis of Pl‐3: Preparation of the Eastern Fragment through a Diastereoselective SmI2‐Mediated Reformatsky Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.201301616openalex-snapshot
Jatrophane Diterpenes: Preparation of the Western Fragment of Pl‐3
inferred← citeshttps://doi.org/10.1002/ejoc.201403598openalex-snapshot
Progress in the Preparation of Jatrophane Diterpenes
inferred← citeshttps://doi.org/10.1002/ejoc.201701668openalex-snapshot
Selectfluor‐Mediated Synthesis of Fluoro Spiro 3(2H)‐Furanone Derivatives via Domino Fluorination–Defluorination
inferred← citeshttps://doi.org/10.1002/ejoc.202400491openalex-snapshot
Preparation and Aldol Couplings of 3(2H)‐Furanones: Stereoselective Synthesis of the C8‐C22 Fragment of Tuscoron A
inferred← citeshttps://doi.org/10.1002/hlca.19900730106openalex-snapshot
Synthetic Studies Directed toward the Pseurotins. Part I. Synthesis of Related Furan‐3(2H)‐ones
inferred← citeshttps://doi.org/10.1002/ijch.197700015openalex-snapshot
Diterpenoid Irritants and Cocarcinogens in Euphorbiaceae and Thymelaeaceae: Structural Relationships in View of their Biogenesis
inferred← citeshttps://doi.org/10.1002/jhet.5570190633openalex-snapshot
A new synthesis of 3(2H)‐furanones from acetylenic β‐diketones
inferred← citeshttps://doi.org/10.1007/10201616_17openalex-snapshot
C20H20 - C20H28 (3790 - 3861)
inferred← citeshttps://doi.org/10.1007/10201616_55openalex-snapshot
Subst. Nos. 3572 - 4112
inferred← citeshttps://doi.org/10.1007/3-540-46100-0_6openalex-snapshot
Phosphonate Chemistry and Reagents in the Synthesis of Biologically Active and Natural Products
inferred← citeshttps://doi.org/10.1007/978-1-4614-4806-8_24openalex-snapshot
Phorbol Esters and Other Toxic Constituents of Jatropha curcas L.
inferred← citeshttps://doi.org/10.1007/978-1-4614-4915-7_20openalex-snapshot
Genetic Diversity, Molecular Markers and Marker Assisted Breeding in Jatropha
inferred← citeshttps://doi.org/10.1007/978-1-4614-4915-7_21openalex-snapshot
Interspecific Hybridization in the Genus Jatropha
inferred← citeshttps://doi.org/10.1007/978-1-4614-4915-7_31openalex-snapshot
Toward the Metabolomics of Jatropha curcas
inferred← citeshttps://doi.org/10.1007/978-1-4684-0823-2_8openalex-snapshot
Advances in the Chemistry of Tumor-Inhibitory Natural Products
inferred← citeshttps://doi.org/10.1007/978-1-4684-8309-3_3openalex-snapshot
Search for Carcinogenic Principles
inferred← citeshttps://doi.org/10.1007/978-1-4757-2085-3_10openalex-snapshot
J
inferred← citeshttps://doi.org/10.1007/978-1-4899-3420-8_3openalex-snapshot
Terpenes (Including Steroids)
inferred← citeshttps://doi.org/10.1007/978-1-4899-4513-6_4openalex-snapshot
Diterpenoids
inferred← citeshttps://doi.org/10.1007/978-1-4899-5196-0_8openalex-snapshot
Advances in the Chemistry of Tumor-Inhibitory Natural Products
inferred← citeshttps://doi.org/10.1007/978-1-4899-6926-2_3openalex-snapshot
Terpenes (including Steroids)
inferred← citeshttps://doi.org/10.1007/978-3-0348-9283-4_95openalex-snapshot
Euphorbiaceae
inferred← citeshttps://doi.org/10.1007/978-3-319-13401-7_6openalex-snapshot
Plant Growth-Promoting Rhizobacteria (PGPR): Emergence and Future Facets in Medicinal Plants
inferred← citeshttps://doi.org/10.1007/978-3-642-58928-7_10openalex-snapshot
J
inferred← citeshttps://doi.org/10.1007/978-3-642-66682-7_6openalex-snapshot
Plant Mono-, Di- and Sesquiterpenoids with Pharmacological or Therapeutical Activity
inferred← citeshttps://doi.org/10.1007/978-3-642-74075-6_31openalex-snapshot
Pharmacologically Active Secondary Metabolites from Wood
inferred← citeshttps://doi.org/10.1007/978-3-7091-8714-2_1openalex-snapshot
Pro-Inflammatory, Tumour-Promoting and Anti-Tumour Diterpenes of the Plant Families Euphorbiaceae and Thymelaeaceae
inferred← citeshttps://doi.org/10.1007/978-981-13-3104-6_20openalex-snapshot
Jatropha: Phytochemistry, Pharmacology, and Toxicology
inferred← citeshttps://doi.org/10.1007/bf00557742openalex-snapshot
Synthesis of macrocyclic compounds that are condensed with a pyrazole ring
inferred← citeshttps://doi.org/10.1007/bf01160484openalex-snapshot
Crystal and molecular structure of hydroxyjatrophone C
inferred← citeshttps://doi.org/10.1007/bf01161150openalex-snapshot
Crystal and molecular structure of 1R,3S,5S,7R,10R-3,6,6,10,14-Pentamethyltricyclo[10.3.0.05,7]pentadeca-11,14-diene-1, 10-dihydroxy-2,13-dione (Japodagrol), C20H28O4
inferred← citeshttps://doi.org/10.1007/s10530-016-1052-2openalex-snapshot
Germplasm, chemical constituents, biological activities, utilization, and control of Chinese tallow (Triadica sebifera (L.) Small)
inferred← citeshttps://doi.org/10.1007/s11094-012-0693-4openalex-snapshot
Isolation and characterization of a new anticancer diterpenoid from Jatropha gossypifolia
inferred← citeshttps://doi.org/10.1007/s11101-020-09667-8openalex-snapshot
Jatrophane and rearranged jatrophane-type diterpenes: biogenesis, structure, isolation, biological activity and SARs (1984–2019)
inferred← citeshttps://doi.org/10.1007/s11101-023-09894-9openalex-snapshot
Nanocarrier mediated co-delivery of phytochemicals and chemo-drugs: an emerging strategy to combat lung cancer in a systemic way
inferred← citeshttps://doi.org/10.1007/s11434-012-5655-4openalex-snapshot
New terpenoids from the roots of Jatropha curcas
inferred← citeshttps://doi.org/10.1007/s13659-013-0031-xopenalex-snapshot
New jatropholane-type diterpenes from Jatropha curcas cv. Multiflorum CY Yang
inferred← citeshttps://doi.org/10.1016/0005-2744(73)90106-xopenalex-snapshot
Reaction of biological thiols with the tumor inhibitor of jatrophone Inhibition of RNA polymerase
inferred← citeshttps://doi.org/10.1016/0009-2797(91)90030-bopenalex-snapshot
Cell-cycle specific cytotoxicity mediated by stizophyllin (2α,3β,12β-trihydroxypregna-4,7,16-trien-20-one), a novel electrophilic pregnane isolated from Stizophyllum riparium
inferred← citeshttps://doi.org/10.1016/0014-5793(81)81240-9openalex-snapshot
On the interaction between jatrophone and DNA
inferred← citeshttps://doi.org/10.1016/0014-5793(83)80017-9openalex-snapshot
Study of the binding of jatrophone to Escherichia coli s‐ribonucleic acid
inferred← citeshttps://doi.org/10.1016/0031-9422(75)83098-6openalex-snapshot
Casbene: An anti-fungal diterpene produced in cell-free extracts of Ricinus communis seedlings
inferred← citeshttps://doi.org/10.1016/0031-9422(84)83091-5openalex-snapshot
Irritant phorbol derivatives from four Jatropha species
inferred← citeshttps://doi.org/10.1016/0031-9422(89)80360-7openalex-snapshot
Diterpenes from Euphorbia helioscopia
inferred← citeshttps://doi.org/10.1016/0040-4020(75)80038-xopenalex-snapshot
Constituents of coper-spurge seed (lathyridis seed)—II
inferred← citeshttps://doi.org/10.1016/b978-0-08-092428-1.50013-6openalex-snapshot
10.1016/b978-0-08-092428-1.50013-6
inferred← citeshttps://doi.org/10.1016/b978-0-12-450280-2.50013-2openalex-snapshot
Evolution of a Synthetic Strategy: Total Synthesis of Jatrophone
inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.11.014openalex-snapshot
Multifidone: A novel cytotoxic lathyrane-type diterpene having an unusual six-membered A ring from Jatropha multifida
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.08.027openalex-snapshot
New tetracyclic triterpenoids from Jatropha gossypiifolia induce cell-cycle arrest and apoptosis in RKO cells
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104707openalex-snapshot
Chemical profile and gastroprotective effect of Jatropha elliptica (Pohl) Oken roots
inferred← citeshttps://doi.org/10.1016/j.jep.2019.01.022openalex-snapshot
Jatropha gossypiifolia L. and its biologically active metabolites: A mini review
inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.05.021openalex-snapshot
Antibacterial diterpenoids from Jatropha podagrica Hook
inferred← citeshttps://doi.org/10.1016/j.phytochem.2008.08.011openalex-snapshot
Diterpenoids from Jatropha multifida
inferred← citeshttps://doi.org/10.1016/j.phytochem.2012.10.009openalex-snapshot
Medicinal property, phytochemistry and pharmacology of several Jatropha species (Euphorbiaceae): A review
inferred← citeshttps://doi.org/10.1016/j.phytochem.2015.07.002openalex-snapshot
Cytotoxic diterpenoids from Jatropha curcas cv. nigroviensrugosus CY Yang Roots
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.125openalex-snapshot
Enynone dihydroxylation–cyclisation as a route to densely functionalised 3(2H)-furanone derivatives: an approach to the core of the zaragozic acids
inferred← citeshttps://doi.org/10.1016/j.tetasy.2016.11.006openalex-snapshot
Absolute configuration of diterpenoids from Jatropha dioica by vibrational circular dichroism
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.03.080openalex-snapshot
Efforts toward the total synthesis of a jatrophane diterpene
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.05.024openalex-snapshot
Synthesis of vinyliodides: progress toward the total synthesis of a jatrophane diterpene
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.09.056openalex-snapshot
Organocatalytic asymmetric synthesis of 3(2H)-furanones with adjacent quaternary and tertiary stereocenters
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.10.150openalex-snapshot
Enantioselective Michael addition of 3(2H)-furanones to α,β-unsaturated aldehydes catalyzed by a diphenylprolinol silyl ether
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.09.128openalex-snapshot
Synthetic studies directed toward the total synthesis of a jatrophane diterpene
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154040openalex-snapshot
Jatrophenediol, a pseudoguaiane sesquiterpenoid from Jatropha dioica rhizomes
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)80273-3openalex-snapshot
Lathyrane type diterpenoid esters from Euphorbia characias
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)83470-6openalex-snapshot
Derivatives of characiol, macrocyclic diterpene esters of the jatrophane type from Euphorbia characias
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)98551-0openalex-snapshot
A diterpene from Euphorbia maddeni
inferred← citeshttps://doi.org/10.1016/s0031-9422(97)01011-xopenalex-snapshot
A Tetracyclic diterpene and triterpenes from euphorbia segetalis
inferred← citeshttps://doi.org/10.1016/s0031-9422(98)00727-4openalex-snapshot
Gossypidien, a lignan from stems of Jatrophagossypifolliafn1fn1Part 29 in the series Studies onPhytochemicals. For Part 28 see Das, B., and Venkataiah,B. (1998). Biochem. Syst. Ecol., in press. iictCommunication No. 4148.
inferred← citeshttps://doi.org/10.1016/s0040-4020(00)00278-7openalex-snapshot
Serrulatin A and B, New Diterpene Polyesters from Euphorbia serrulata
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)93309-5openalex-snapshot
Structure and stereochemistry of bertyadionol
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)71453-5openalex-snapshot
Synthesis of geiparvarin: a novel antitumor agent possessing a 3(2H)-furanone ring
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)72236-2openalex-snapshot
The structure of kansuinine A, a new multi-oxygenated diterpene
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)72238-6openalex-snapshot
Kansuinine B, a novel multi-oxygenated diterpene from euphorbia kansui liou.
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)84550-5openalex-snapshot
Isolation and structure determination of four novel diterpenes from jatropha curcus
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)86953-1openalex-snapshot
Synthesis of chiral cyclopentenoids
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)86067-6openalex-snapshot
Jatropholones A and B, new diterpenoids from the roots of (euphorbiaceae) - crystal structure analysis of Jatropholone B.
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)92490-6openalex-snapshot
The isolation and structures of euphoscopins a and b
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)00704-4openalex-snapshot
A novel 8,9-seco-rhamnofolane and a new rhamnofolane endoperoxide from Jatropha integerrima roots
inferred← citeshttps://doi.org/10.1016/s0099-9598(08)60186-8openalex-snapshot
Chapter 1 Antitumor Alkaloids
inferred← citeshttps://doi.org/10.1016/s0176-1617(97)80178-2openalex-snapshot
Accumulation of diterpenoids in cell and root-organ cultures of Jatropha species
inferred← citeshttps://doi.org/10.1016/s0305-1978(00)00049-1openalex-snapshot
A minor coumarino-lignoid from Jatropha gossypifolia
inferred← citeshttps://doi.org/10.1016/s0305-1978(03)00067-xopenalex-snapshot
Cleomiscosin A, a coumarino-lignoid from Jatropha gossypifolia
inferred← citeshttps://doi.org/10.1016/s1054-3589(08)60266-5openalex-snapshot
Computer-Assisted Structure-Activity Correlations
inferred← citeshttps://doi.org/10.1016/s1874-6004(04)80009-1openalex-snapshot
Total Synthesis of Jatrophatrione, an Unprecedented [5.9.5] Tricyclic Antileukemic Diterpene
inferred← citeshttps://doi.org/10.1017/s1751731107000298openalex-snapshot
Bioactivity of phytochemicals in some lesser-known plants and their effects and potential applications in livestock and aquaculture production systems
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00511openalex-snapshot
Advanced Structural Determination of Diterpene Esters Using Molecular Modeling and NMR Spectroscopy
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b01036openalex-snapshot
Antitumor Activity of Diterpenoids from Jatropha gossypiifolia: Cell Cycle Arrest and Apoptosis-Inducing Activity in RKO Colon Cancer Cells
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00885openalex-snapshot
Successive Promotion of Formal [3+2] Cycloaddition of Aryl Methyl Ketones by I2 and Zn: Access to 2-Hydroxy-4-morpholin-2,5-diarylfuran-3(2H)-ones with a Quaternary Carbon Center
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01147openalex-snapshot
Construction of the Bicyclic Carbon Framework of Euphosalicin
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02350openalex-snapshot
A Serendipitous Synthesis of Bis-Heterocyclic Spiro 3(2H)-Furanones
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02505openalex-snapshot
Lewis-Acid-Catalyzed Asymmetric Alkynylation of Alkynyl 1,2-Diketones: Controllable Formation of 3(2H)-Furanones and α-Hydroxy Ketones
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03469openalex-snapshot
Cooperative Rh(II)/Pd(0) Dual Catalysis: Synthesis of Highly Substituted 3(2H)-Furanones with a C2-Quaternary Center via a Cyclization/Allylic Alkylation Cascade of α-Diazo-δ-keto-esters
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03649openalex-snapshot
Euphylonoids A and B, Two Highly Modified Jatrophane Diterpenoids with Potent Lipid-Lowering Activity from Euphorbia hylonoma
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01196openalex-snapshot
Rh(II)-Catalyzed Chemoselective Oxy-alkynylation of Acceptor–Acceptor Carbenes: Synthesis of C2-Quaternary Alkyne-Substituted 3(2H)-Furanones
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03039openalex-snapshot
Enantioselective Conjugate Additions of 2-Alkoxycarbonyl-3(2H)-furanones
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04029openalex-snapshot
Jatrofolianes A and B: Two Highly Modified Lathyrane Diterpenoids from Jatropha gossypiifolia
inferred← citeshttps://doi.org/10.1021/ja021177ropenalex-snapshot
Concise Total Syntheses of the Bioactive Mesotricyclic Diterpenoids Jatrophatrione and Citlalitrione
inferred← citeshttps://doi.org/10.1021/ja303023nopenalex-snapshot
Highly Stereoselective C–C Bond Formation by Rhodium-Catalyzed Tandem Ylide Formation/[2,3]-Sigmatropic Rearrangement between Donor/Acceptor Carbenoids and Chiral Allylic Alcohols
inferred← citeshttps://doi.org/10.1021/jo802581gopenalex-snapshot
Synthetic Studies toward Jatrophane Diterpenes from Euphorbia characias. Enantioselective Synthesis of (−)-15-O-Acetyl-3-O-propionyl-17-norcharaciol
inferred← citeshttps://doi.org/10.1021/jo9825254openalex-snapshot
Studies Directed toward the Synthesis of the Unusual Antileukemic Diterpene Jatrophatrione. 1. A Solution to the Problem of Chirality Merger during Elaboration of the Entire Carbotricyclic Framework
inferred← citeshttps://doi.org/10.1021/np300832nopenalex-snapshot
Cytotoxic Phorbol Esters of Croton tiglium
inferred← citeshttps://doi.org/10.1021/ol902221yopenalex-snapshot
General Synthesis of Highly Functionalized Cyclopentane Segments for the Preparation of Jatrophane Diterpenes
inferred← citeshttps://doi.org/10.1021/ol902349fopenalex-snapshot
Jatrophalactam, A Novel Diterpenoid Lactam Isolated from Jatropha curcas
inferred← citeshttps://doi.org/10.1039/b701548hopenalex-snapshot
A catalytic asymmetric protocol for the enantioselective synthesis of 3(2H)-furanones
inferred← citeshttps://doi.org/10.1080/00397917808063569openalex-snapshot
Conjugated Addition to 2,2-Dimethyl-3(2h)-furanone: Support for the Baldwin Rules for Ring Closure
inferred← citeshttps://doi.org/10.1080/10915810701464641openalex-snapshot
Phorbol Esters: Structure, Biological Activity, and Toxicity in Animals
inferred← citeshttps://doi.org/10.1080/14786411003792207openalex-snapshot
A new macrocyclic diterpenoid fromJatropha multifida
inferred← citeshttps://doi.org/10.1111/j.1095-8339.1987.tb01039.xopenalex-snapshot
Members of Euphorbiaceae in primitive and advanced societies
inferred← citeshttps://doi.org/10.1155/2012/846583openalex-snapshot
Bioactivity Evaluation of Plant Extracts Used in Indigenous Medicine against the Snail,Biomphalaria glabrata, and the Larvae ofAedes aegypti
inferred← citeshttps://doi.org/10.1155/2014/369204openalex-snapshot
Jatropha gossypiifolia L. (Euphorbiaceae): A Review of Traditional Uses, Phytochemistry, Pharmacology, and Toxicology of This Medicinal Plant
inferred← citeshttps://doi.org/10.1155/2014/604152openalex-snapshot
Medicinal Plants and Other Living Organisms with Antitumor Potential against Lung Cancer
inferred← citeshttps://doi.org/10.1177/1934578x0800301012openalex-snapshot
Guaiane Sesquiterpenoids from Jatropha curcas
inferred← citeshttps://doi.org/10.1177/1934578x1200700204openalex-snapshot
A Novel Anticancer Diterpenoid from Jatropha Gossypifolia
inferred← citeshttps://doi.org/10.1246/bcsj.56.3078openalex-snapshot
Regiocontrolled Formation of 4,5-Dihydro-3(2H)-furanones from 2-Butyne-1,4-diol Derivatives. Synthesis of Bullatenone and Geiparvarin
inferred← citeshttps://doi.org/10.1248/cpb.54.754openalex-snapshot
Quantitative Determination of Jatrophone in "Cachaca" Prepared with Jatropha elliptica
inferred← citeshttps://doi.org/10.13005/bpj/2664openalex-snapshot
Chemical and Biological Profiling of Three Ferulic Acids Alkyl Esters Isolated from Jatropha pandurifolia (Family: Euphorbiaceae) Stem Bark.
inferred← citeshttps://doi.org/10.15517/rbt.v61i3.11906openalex-snapshot
Establecimiento de suspensiones celulares de dos especies Jatropha (Euphorbiaceae) de Costa Rica
inferred← citeshttps://doi.org/10.1590/s0100-736x2008000600003openalex-snapshot
Intoxicação experimental com as folhas de Jatropha gossypifolia (Euphorbiaceae) em ovinos
inferred← citeshttps://doi.org/10.1653/024.094.0330openalex-snapshot
Jatropha gossypiifolia(Euphorbiaceae), a Source of Proteins Toxic toPhenacoccus herreni(Sternorryncha: Pseudococcidae)
inferred← citeshttps://doi.org/10.17576/mjas-2018-2201-08openalex-snapshot
NEW DITERPENOIDS FROM THE ROOTS OF Croton hirtus (EUPHORBIACEAE)
inferred← citeshttps://doi.org/10.2174/1871520621666211108091444openalex-snapshot
Naturally Occurring O-Heterocycles as Anticancer Agents
inferred← citeshttps://doi.org/10.22271/phyto.2025.v14.i3e.15385openalex-snapshot
Phytochemical screening of plant extracts and GC-MS analysis of the n-hexane extracts of stems and roots of Jatropha curcas growing in Bangladesh
inferred← citeshttps://doi.org/10.24820/ark.5550190.p010.285openalex-snapshot
Our phytochemical research on Jatropha species
inferred← citeshttps://doi.org/10.25100/socolen.v32i1.9357openalex-snapshot
Effect of Jatropha Gossypiifolia Leaf Extracts On Three Lepidoptera Species
inferred← citeshttps://doi.org/10.25100/socolen.v32i1.9396openalex-snapshot
REVISTA COLOMBIANA DE ENTOMOLOGÍA Vol 32 No. 1 ENERO - JUNIO 2006 PDF TOTAL
inferred← citeshttps://doi.org/10.3109/13880208009065179openalex-snapshot
Caribbean and Latin American Folk Medicine and Its Influence in the United States
inferred← citeshttps://doi.org/10.3389/fbioe.2018.00160openalex-snapshot
Dynamic Control of ERG20 and ERG9 Expression for Improved Casbene Production in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.3390/ph19050801openalex-snapshot
Triazole-Functionalized Jatrophone Derivatives as Antiprotozoal Agents Against Trypanosoma cruzi: Synthesis, Biological Evaluation and Structure—Activity Relationships
inferred← citeshttps://doi.org/10.7439/ijpr.v3i1.36openalex-snapshot
HPTLC analysis and Anti-inflammatory activity of Jatropha gossypifolia L. root in mice and Wistar rats
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.