Synonym |
Corticotropin |
Species |
Human |
Protein Accession |
P01193 |
Purity |
Greater than 95% as determined by RP-HPLC and SDS-PAGE |
Endotoxin Level |
Less than 1 EU/µg |
Biological Activity |
The activity is determined by the dose-dependent stimulation of the proliferation of mouse Y1
cells is ≤ 1 ng/ml, corresponding to a specific activity of 2 x 10^6 units/mg. |
Expression System |
E. coli |
Fusion Tag |
None |
Predicted Molecular Mass |
Approximately 3944 Da |
Formulation |
Lyophilized from a 0.2 µm filtered solution of 10mM sodium phosphate, pH 7.5 |
Reconstitution |
Centrifuge the vial prior to opening. Reconstitute in water to a concentration of 0.1-1.0 mg/ml.
Do not vortex. |
Storage & Stability |
Store at -20°C. Please refer to product insert for more information. |
FAQ
What is ACTH (7-38) (human) C75H106N20O19S used for, and how does it work?
ACTH (7-38) (human) is
a truncated form of the adrenocorticotropic hormone specifically tailored to omit the first six amino
acids from its full sequence, which alters its receptor-binding affinity and biological activity. The
sequence modification significantly impacts its interaction with the melanocortin receptors in the body.
Typically, ACTH is known for its role in stimulating the adrenal glands to produce cortisol, a critical
steroid hormone that plays a vital role in various bodily functions such as metabolism and immune
response regulation. In contrast, ACTH (7-38) functions mainly as an antagonist or partial agonist,
depending on the receptor subtype it interacts with.
The peptide's truncated nature makes it a
research focus for understanding its role in potential therapeutic applications. It provides a means to
study how modifying peptide chains can alter receptor functions, which is crucial in the development of
drugs targeting these pathways. For instance, novel therapies for inflammatory diseases, stress-related
disorders, or metabolic syndromes may be developed by exploiting the specific pathways that ACTH (7-38)
affects. By precisely modulating the melanocortin pathway, researchers can explore treatment options
that offer fewer side effects than traditional corticosteroid treatments.
Additionally, ACTH
(7-38) is of immense interest in neuroscientific research, where understanding the central mechanisms of
stress and pain is pivotal. By interacting with receptors in the brain, ACTH (7-38) can provide insights
into neuroinflammatory processes and help delineate the effects of melanocortins on brain activity and
function. This peptide can also serve as a tool for exploring the broader physiological roles of ACTH
fragments in processes like pigmentation, energy homeostasis, and other endocrine functions.
In
summation, ACTH (7-38) represents a crucial area of study due to its ability to selectively modulate
specific pathways. Its altered receptor interaction spectrum offers possibilities for novel therapeutic
strategies beyond those achievable with traditional ACTH. This makes it a valuable asset in
pharmacological research and the development of specialized treatment regimens aimed at targeting
specific receptor-mediated pathways within the body.
How does the chemical formula C75H106N20O19S
relate to the function of ACTH (7-38) (human)?
The chemical formula C75H106N20O19S represents the
specific arrangement and number of atoms present in the ACTH (7-38) peptide, reflecting its unique
molecular structure that contributes to its function. This formula indicates that the peptide consists
of 75 carbon atoms, 106 hydrogen atoms, 20 nitrogen atoms, 19 oxygen atoms, and a singular sulfur atom.
This composition plays a crucial role in determining the peptide's physical, chemical, and biological
properties, all of which are essential for its intended research applications.
The sequence of
amino acids in ACTH (7-38) is specifically organized to facilitate interactions with melanocortin
receptors. These interactions are largely determined by the conformation or 3D shape of the peptide,
which is a direct result of its unique chemical structure. The presence of disulfide bonds, which
involve the sulfur atom, might also contribute to the peptide's stable configuration and receptor
specificity. The precise nature of these bonds and interactions is pivotal in influencing the peptide's
binding affinity, selectivity, and biological efficacy.
Understanding the chemical formula is
vital for comprehending the peptide's synthesis and stability. The molecular structure determines how it
can be synthesized chemically, its solubility in various solvents, and its storage conditions.
Mismanagement of these factors could lead to degradation or denaturation, significantly affecting its
function and research utility. Hence, appreciating the chemical formula aids researchers not only in
synthesizing the peptide but also in formulating the right environment for maintaining its
integrity.
Furthermore, examining this molecular structure helps in deciphering the modifications
that could enhance or suppress its biological activity. By altering specific portions of this formula,
researchers can create analogs of ACTH (7-38) that could possess improved pharmacological profiles or
reduced side effects. This process is fundamental in drug development, where enhancing efficacy while
minimizing adverse reactions is a key objective.
In essence, the chemical formula of ACTH (7-38)
is more than a mere string of letters and numbers. It represents the fundamental blueprint that
encompasses the peptide's preparation, stability, and application. This blueprint is crucial in
exploring and expanding the therapeutic potential of ACTH (7-38) and related peptides in scientific
research.
What potential therapeutic applications are envisioned for ACTH (7-38)
(human)?
THERES A LARGE SP AECEETING THIS. pls ignroe.
ACTH (7-38) (human), due to its
selective receptor activity, holds potential in several therapeutic areas, primarily driven by its
unique interactions with melanocortin receptors. One of the most promising areas is in the management
and treatment of inflammatory and autoimmune disorders. By modulating specific pathways involved in
inflammation, ACTH (7-38) could potentially reduce the inflammatory response without inducing the broad
immunosuppressive effects associated with traditional corticosteroid therapies. This could be
particularly beneficial in chronic conditions like rheumatoid arthritis or lupus, where prolonged
steroid use can lead to significant side effects.
In addition to its potential in inflammatory
diseases, ACTH (7-38) might find applications in addressing certain metabolic disorders. Given the role
of melanocortin receptors in regulating energy homeostasis, appetite, and metabolism, selective
modulation by ACTH (7-38) could lead to novel treatments for conditions such as obesity and metabolic
syndrome. By targeting specific receptors, it may be possible to influence metabolic rate, fat storage,
and appetite regulation without impacting other systems adversely.
Another exciting potential
application of ACTH (7-38) is in neuroprotection and neuroinflammation. The central nervous system
expresses several melanocortin receptors, and modulation of these pathways can impact neuroinflammatory
processes. ACTH (7-38) could be beneficial in conditions characterized by neuroinflammation, such as
multiple sclerosis or Alzheimer's disease, potentially slowing progression or alleviating symptoms by
reducing inflammatory damage in neural tissues.
Furthermore, ACTH (7-38) offers opportunities in
addressing disorders related to stress and anxiety. By influencing pathways involved in the stress
response, it's plausible to utilize this peptide in developing therapies for stress-related disorders,
including generalized anxiety disorder or post-traumatic stress disorder (PTSD). Altering stress hormone
levels and the associated physiological responses could lead to better management strategies for these
conditions.
Lastly, there might be potential in the treatment of skin conditions. The
melanocortin pathway is involved in pigment production, so ACTH (7-38) might be explored for disorders
like vitiligo or melanoma, offering ways to modulate melanogenesis or tumor progression. However, this
area requires further exploration to understand the implications fully.
Overall, the potential
therapeutic applications of ACTH (7-38) are expansive. They span various fields of medicine from
dermatology to neurology and endocrinology, embodying the versatility and promise of peptide-based
interventions in modern therapeutics.
Are there any known side effects or risks associated with
ACTH (7-38) (human) use in research?
When delving into the potential side effects or risks
associated with ACTH (7-38) (human), it's essential to note that the peptide is currently more
associated with research settings rather than clinical application. As a result, comprehensive side
effect profiling akin to that completed for approved pharmaceutical drugs is not yet fully established.
However, understanding the possible side effects through preliminary research and analogous compounds
can offer insight into what researchers might anticipate.
ACTH (7-38) interacts with melanocortin
receptors, which play a role in a variety of physiological processes. Consequently, unintended
modulation of these receptors can potentially lead to off-target effects, such as alterations in
metabolic activity, appetite, or weight, particularly given the role of melanocortins in regulating
energy homeostasis. While precise effects are largely hypothetical without conclusive clinical trials,
these pathways suggest possible areas of concern.
In an inflammatory context, although ACTH
(7-38) could potentially suppress undesirable immune responses, there is always a risk that modifying
immune function might lead to an increased susceptibility to infections or impaired healing, mirroring
issues seen with broad-spectrum immunosuppressants or corticosteroids. This necessitates careful
monitoring in a research setting to understand the balance and potential immune-related
risks.
Moreover, when discussing neurological pathways, any peptide capable of influencing
receptors in the brain carries with it the concern of impacting mood or cognitive function. Effects on
mood stabilization, anxiety levels, or cognitive clarity could arise, necessitating thorough assessment
and cautious interpretation during preclinical trials.
An additional consideration is the
peptide's pharmacokinetics, which determines its half-life, distribution, and elimination in the body.
Any issues in these areas could contribute to either diminished efficacy or prolonged exposure, leading
to potential adverse effects that could complicate its use.
Chemical synthesis and purity of ACTH
(7-38) also demand attention. Impurities or inaccuracies in peptide formulation could result in
unintended biological effects or toxicity. Therefore, ensuring high purity and structural accuracy
through rigorous quality control is pivotal in reducing adverse risks.
In sum, while ACTH (7-38)
presents promising research potential, the associated risks and side effects require comprehensive
exploration and evaluation. These efforts will help establish a safety profile crucial for progressing
from research applications to potential clinical trials and therapeutic use. As such, ongoing studies
and trials are essential to fully understand the safety and side effect profile of this promising
peptide in various biological contexts.
How does ACTH (7-38) (human) compare to the full-length
ACTH in terms of biological activity?
ACTH (7-38) (human) differs significantly from the
full-length adrenocorticotropic hormone (ACTH), particularly with respect to its biological activity and
interaction with receptors. The full-length ACTH peptide, known primarily for its 1-39 amino acid
sequence, has a well-documented role in stimulating the adrenal cortex to produce glucocorticoids like
cortisol, which are crucial in stress response, metabolism, and immune modulation. This full spectrum of
activity is facilitated by its structure, which allows it to effectively bind to melanocortin receptor
type 2 (MC2R) on the adrenal glands.
In contrast, ACTH (7-38) lacks the first six amino acids of
the full-length protein, including critical regions involved in the potent activation of MC2R. As a
result, ACTH (7-38) is significantly less effective or even inactive in inducing adrenal hormone
production. Instead, this peptide acts more selectively as an antagonist or a partial agonist at other
melanocortin receptors (such as MC3R, MC4R, and MC5R), altering its functional landscape
entirely.
This shift allows ACTH (7-38) to be used primarily as a research tool to explore
non-steroidogenic pathways of melanocortin receptor signaling. For instance, it can shed light on
neuropeptide functions in the central nervous system, such as appetite regulation, energy homeostasis,
and neuroinflammation—domains where the full-length ACTH would activate several pathways
indistinguishably. Additionally, because ACTH (7-38) can more selectively modulate certain receptors,
researchers can study its potential use in treating diseases where immune or metabolic modulation is
needed without direct adrenal steroidogenesis.
Furthermore, in the context of receptor
specificity, ACTH (7-38) provides insights into the decoupling of steroidogenesis from other biological
actions elicited by melanocortins, which is invaluable in drug development. This nature of selective
receptor interaction holds promise for crafting therapies that need the benefit of ACTH-related pathways
minus the extensive cortisol-related side effects, such as in precisely tailored desensitization or
anti-inflammatory therapies.
In conclusion, while the full-length ACTH serves as a potent
activator across multiple pathways, ACTH (7-38) offers a more nuanced approach. It acts where finer
control of specific melanocortin receptor pathways is crucial, such as in research focused on broader
physiological processes or conditions requiring specific receptor targeting without generalized adrenal
activation. This distinction makes ACTH (7-38) crucial to understanding and manipulating specific
signaling pathways with greater specificity and potentially fewer systemic effects.