These are the chemical structure drawings I created with BKchem, BIOVIA Draw and Inkscape. All images are scalable vector graphics and (unless noted otherwise) released into the public domain:
New chemical formulae edit
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A 276575, a SEGRA -
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Acetylamifampridine -
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ACT-132577, the active metabolite of macitentan -
Antibody with CDRs -
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Afatinib binding to EGFR -
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Alfatradiol compared to estradiol -
Anemoninsäure -
Ambrisentan (stereochemistry) -
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BIBF 1202, the main metabolite of nintedanib -
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Branaplam keto-enol tautomerism -
Bromfenac cyclic amide -
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Carbamazepine metabolism -
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Catumaxomab mechanism -
(−)-α-Cedrene -
(+)-β-Cedrene -
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Version with CDRs -
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Activation of clopidogrel -
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Colestilan, alternative structure -
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Colestipol, alternative structure -
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Dabigatran etexilate -
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Dihydrostreptazolin -
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Enalkiren (another orientation) -
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Engineered monoclonal antibodies -
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Epimerox, compound 1 -
Epimerox, compound 2 -
Epimerox synthesis -
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Eritoran acid -
Eritoran tetrasodium -
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FR for C-glycosides -
Nitrogen analog of the FR -
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Other tautomer of foliglurax -
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Heavy-chain and common antibody -
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Hydroxyethyl succinimide, a metabolite of diroximel fumarate -
Hydroxylornoxicam, the metabolite of lornoxicam -
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ID-11614 and ID-20219, metabolites of lurasidone -
ID-14283, active metabolite of lurasidone -
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(R)-D-Isoglutamine -
(S)-L-Isoglutamine -
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LBQ657, the active metabolite of sacubitril -
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Lenvatinib metabolism -
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Levocetirizine (stereochemistry) -
Levodopa activation and inactivation -
Levofolinic acid (stereochemistry) -
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Lorlatinib metabolism -
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Chelator of lutetium (177Lu) lilotomab satetraxetan -
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Comparison of cis and trans mefway -
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Mertansine plus mab -
Mertansine plus mab, colour coded -
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MK-5932, a SEGRA -
Monomethyl auristatin E-mab-conjugate -
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Monomethyl auristatin F-mab-conjugate -
Morphine (stereochemistry) -
MRE 269, the active metabolite of selexipag -
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Netupitant metabolites -
Octahydrophenanthrene-2,7-diol type SEGRA -
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Synthesis of olaflur -
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Opicapone and metabolites -
Oteracil potassium -
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Palonosetron metabolites -
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Pegaptanib sodium -
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Phosphorothioate DNA of an antisense oligonucleotide -
Phosphorothioate RNA of an antisense oligonucleotide -
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Activation of prasugrel -
Active metabolite of prasugrel -
Prostamide E2 -
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Quadroma antibodies -
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RU 24858, a SEGRA -
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SIN-1A, the active metabolite of molsidomine -
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scFv, polyvalent -
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Sodium alkyl sulfates -
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Spilanthol from Acmella oleracea -
Another Acmella oleracea amide -
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Tafluprost metabolism -
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E-Teriflunomide -
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Ticagrelor metabolite -
TL 12-186, a proteolysis targeting chimera -
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Tofogliflozin -
Tofogliflozin monohydrate -
Tolcapone metabolism -
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Trifluoroisopropanolamine / amide type SEGRAs -
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Valproic acid metabolism -
Vandetanib metabolism -
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ZK 216348, a SEGRA -
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_mebrofenin_skeletal.svg)
Vectorised chemical formulae edit
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Azathioprine metabolism (added formulae) -
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Betaenones A, B and C -
Betaenone B biosynthesis -
Butenyl-methyl-L-threonine biosynthesis -
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The PDE3 inhibitor CI-930 (stereochemistry) -
CI-930 with its heterocycle – phenyl – imidazole pattern -
Cisplatin synthesis -
Cisplatin and transplatin -
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DOTA (tetraxetan) -
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Eledoisin (stereochemistry) -
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Ferrier carbocyclization (FCC) -
Mechanism of the FCC -
FCC continued -
Sinaÿ's modification of the FCC -
Proposed transition state for Sinaÿ's modification of the FCC -
Planar chiral ferrocene derivative -
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Gitoformate (stereochemistry) -
Metabolic pathways of gamma-hydroxybutyric acid -
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HU-320 (stereochemistry) -
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Incarvillateine (stereochemistry) -
Levobetaxolol (stereochemistry) -
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Lornoxicam (tautomerism) -
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(-)-Menthone -
(+)-Menthone -
Meribendan (stereochemistry) -
Metapramine (stereochemistry) -
Methylenedioxy group -
2-Methyl-MDA (stereochemistry) -
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Octamoxin (stereochemistry) -
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Synthesis of rapamycin from prerapamycin -
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"Protonated" rhodocene -
Proton pump inhibitors mechanism -
Proton pump inhibitors structure -
PTMEG synthesis -
Rhodocene dimerisation -
Decaisopropylrhodicinium hexafluorophosphate synthesis -
Staggered ferrocene and eclipsed ruthenocene -
Synthesis of the 1-cobaltocenyl-1'-rhodocenylferrocene cation -
Bi- and ter-metallocenes containing rhodocenyl groups -
Synthesis of the 1,2,3-tri-tert-butylrhodocenium cation -
Rivaroxaban (stereochemistry) -
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Sofosbuvir mechanism -
SRT2183 (stereochemistry) -
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Truxillic and truxinic acid stereochemistry -
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-Menthone_structure.svg)
-Menthone_structure.svg)
Rh(C5H5))BF4.svg)
