General Information of the Compound
Compound ID
CP0035923
Compound Name
(S)-2-((S)-1-((S)-2-((S)-2-((S)-2-((S)-2-((S)-5-(diaminomethyleneamino)-2-(2-(methylamino)acetamido)pentanamido)-3-methylbutanamido)-3-(4-hydroxyphenyl)propanamido)-3-methylbutanamido)-3-(1H-imidazol-5-yl)propanoyl)pyrrolidine-5-carboxamido)propanoic acid
    Show/Hide
Synonyms
(1-(N-Methylglycin) 5-L-valin, 8-L-alanin)angiotensin II
(Sar1,Val5,Ala8)-Angiotensin II
34273-10-4
AC1O44IX
Angiotensin II, 1-(N-methylglycine)-5-L-valine-8-L-alanine-
CHEMBL938
DSSTox_RID_81710
H2AFV2HE66
N-(1-(N-(N-(N-(N-(N2-(N-methylglycly)-L-arginyl)-L-valyl)-L-tyrosyl)-L-valyl)-L-histidyl)-L-prolyl)-L-alanine
NCGC00166135-01
SARALASIN
SCHEMBL23
Saralasin
Saralasin [INN:BAN]
Saralasina
Saralasina [INN-Spanish]
Saralasine
Saralasine [INN-French]
Saralasinum
Saralasinum [INN-Latin]
UNII-H2AFV2HE66
    Show/Hide
Structure
Formula
C42H65N13O10
Molecular Weight
912.063
Canonical SMILES
CNCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(O)=O
    Show/Hide
InChI
InChI=1S/C42H65N13O10/c1-22(2)33(53-35(58)28(50-32(57)20-45-6)9-7-15-47-42(43)44)38(61)51-29(17-25-11-13-27(56)14-12-25)36(59)54-34(23(3)4)39(62)52-30(18-26-19-46-21-48-26)40(63)55-16-8-10-31(55)37(60)49-24(5)41(64)65/h11-14,19,21-24,28-31,33-34,45,56H,7-10,15-18,20H2,1-6H3,(H,46,48)(H,49,60)(H,50,57)(H,51,61)(H,52,62)(H,53,58)(H,54,59)(H,64,65)(H4,43,44,47)/t24-,28-,29-,30-,31-,33-,34-/m0/s1
    Show/Hide
InChIKey
PFGWGEPQIUAZME-NXSMLHPHSA-N
CAS
34273-10-4
Physicochemical Property
logP
-2.5102
Rotatable Bonds
25
Heavy Atom Count
65
Polar Areas
357.55
Hydrogen Bond Donor Count
12
Hydrogen Bond Acceptor Count
12
Complexity
65

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

    Show/Hide
Click to Show/Hide the External Link(s) of This Compound
PubChem ID
CID: 6324663
SID: 14816411
ChEMBL ID
CHEMBL938
DrugBank ID
DB06763
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT01197, Type-1 angiotensin II receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  3
1
EC50 = 11 nM
   TI
   LI
   LO
   TS
2
EC50 > 10000 nM
   TI
   LI
   LO
   TS
3
IC50 = 0.4 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 0.35 nM
2 IC50 = 0.57 nM
3 IC50 = 0.6 nM
4 IC50 = 0.67 nM
5 IC50 = 1 nM
6 Ki = 0.17 nM
7 Ki = 0.22 nM
8 Ki = 0.33 nM
Protein ID: PT04214, Type-1 angiotensin II receptor A
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  2
1
EC50 = 6 nM
   TI
   LI
   LO
   TS
2
EC50 = 7.5 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( SARALASIN )
Drug Name SARALASIN
Indication
Hypertension
Approved
Target(s)
Angiotensin II receptor type-1 (AGTR1)
Inhibitor
Angiotensin II receptor type-2 (AGTR2)
Inhibitor