General
Preferred name
INTERMEDINE
Synonyms
CZEN-002 ()
α-MSH ()
α-Melanocyte-Stimulating Hormone ()
alpha-MSH TFA ()
¦Á-MSH TFA, ¦Á-MSH Trifluoroacetate, alpha-MSH Trifluoroacetate, ¦Á-Melanocyte-stimulating hormone TFA, ¦Á-Melanocyte-stimulating hormone Trifluoroacetate ()
Melanotropin alpha ()
.alpha.-melanotropin (human) ()
ALPHA-MSH ()
.alpha.-melanotropin ()
.alpha.-melanotropin (ox) ()
Melanotropin ()
Melanophore-stimulating hormone ()
.alpha.-melanotropin (sheep) ()
N-acetyl-acth(1-13)-amide ()
Intermedin ()
Melantropin ()
.alpha.-msh ()
Alpha-melanocyte stimulating hormone ()
?-MSH (human, mouse, rat, porcine, bovine, ovine) (trifluoroacetate salt) ()
P&D ID
PD079431
CAS
581-05-5
171869-93-5
Tags
available
drug candidate
Drug indication
Fungal infection
Drug Status
investigational
Max Phase
Phase 1
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure
P&D probe-likeness score
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Cell lines
0
Organisms
1
Compound Sets
5
Cayman Chemical Bioactives
ChEMBL Drugs
DrugMAP
MedChem Express Bioactive Compound Library
Selleckchem Bioactive Compound Library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
33
Properties
(calculated by RDKit )
Molecular Weight
1663.79
Hydrogen Bond Acceptors
22
Hydrogen Bond Donors
23
Rotatable Bonds
50
Ring Count
6
Aromatic Ring Count
5
cLogP
-4.54
TPSA
642.98
Fraction CSP3
0.49
Chiral centers
12.0
Largest ring
6.0
QED
0.01
Structural alerts
0
No structural alerts detected
Related compounds
Custom attributes
(extracted from source data)
Pathway
GPCR/G protein
Neuronal Signaling
Target
Melanocortin Receptor
Source data
