TY - JOUR
T1 - Current Perspectives on Pyrroloiminoquinones
T2 - Distribution, Biosynthesis and Drug Discovery Potential
AU - Kalinski, Jarmo Charles J.
AU - Polyzois, Alexandros
AU - Waterworth, Samantha C.
AU - Siwe Noundou, Xavier
AU - Dorrington, Rosemary A.
N1 - Publisher Copyright:
© 2022 by the authors.
PY - 2022/12
Y1 - 2022/12
N2 - Pyrroloiminoquinones are a group of cytotoxic alkaloids most commonly isolated from marine sponges. Structurally, they are based on a tricyclic pyrrolo[4,3,2-de]quinoline core and encompass marine natural products such as makaluvamines, tsitsikammamines and discorhabdins. These diverse compounds are known to exhibit a broad spectrum of biological activities including anticancer, antiplasmodial, antimicrobial, antifungal and antiviral activities as well as the inhibition of several key cellular enzymes. The resurgence of interest in pyrroloiminoquinones and the convoluted understanding regarding their biological activities have prompted this review. Herein, we provided a concise summary of key findings and recent developments pertaining to their structural diversity, distribution, biogenesis, and their potential as chemical probes for drug development, including a discussion of promising synthetic analogs.
AB - Pyrroloiminoquinones are a group of cytotoxic alkaloids most commonly isolated from marine sponges. Structurally, they are based on a tricyclic pyrrolo[4,3,2-de]quinoline core and encompass marine natural products such as makaluvamines, tsitsikammamines and discorhabdins. These diverse compounds are known to exhibit a broad spectrum of biological activities including anticancer, antiplasmodial, antimicrobial, antifungal and antiviral activities as well as the inhibition of several key cellular enzymes. The resurgence of interest in pyrroloiminoquinones and the convoluted understanding regarding their biological activities have prompted this review. Herein, we provided a concise summary of key findings and recent developments pertaining to their structural diversity, distribution, biogenesis, and their potential as chemical probes for drug development, including a discussion of promising synthetic analogs.
KW - Acarnidae
KW - Latrunculiidae
KW - batzelline
KW - damirone
KW - discorhabdin
KW - epinardin
KW - makaluvamine
KW - prianosin
KW - sponges
KW - tsitsikammamine
UR - http://www.scopus.com/inward/record.url?scp=85144564676&partnerID=8YFLogxK
U2 - 10.3390/molecules27248724
DO - 10.3390/molecules27248724
M3 - Review article
C2 - 36557854
AN - SCOPUS:85144564676
SN - 1420-3049
VL - 27
JO - Molecules
JF - Molecules
IS - 24
M1 - 8724
ER -