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    • Affinities for the different receptors are shown in the first line. To read the reference, click on the affinity you are interested in.
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    CHEMBL211600


    Show docking results

    Inhibition of:
    ASIC: 17 nM (ic50)
    Synonymous names
    CHEMBL211600
    CHEBI:452478
    SmilesC1=CC(=CC(=C1)OCCO)CCCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N
    11553569 
     
    16821771
    FormulaC18H24ClN7O3
    Molweight421.881
    Heavy Atoms29
    Rotatable Bonds10
    H-bond donors5
    H-bond Acceptors 8
    Cluster numberCluster408


    CHEMBL379433


    Show docking results

    Inhibition of:
    ASIC: 20 nM (ic50)
    Synonymous names
    CHEMBL379433
    CHEBI:452444
    SmilesC1=CC(=CC=C1CCCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N)OCCC(=O)O
    11562155 
     
    16821771
    FormulaC19H24ClN7O4
    Molweight449.891
    Heavy Atoms31
    Rotatable Bonds11
    H-bond donors5
    H-bond Acceptors 9
    Cluster numberCluster408


    CHEMBL379066


    Show docking results

    Inhibition of:
    ASIC: 30 nM (ic50)
    Synonymous names
    CHEMBL379066
    CHEBI:452395
    SmilesC1=CC=C(C(=C1)CCCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N)O
    11574400 
     
    16821771
    FormulaC16H20ClN7O2
    Molweight377.829
    Heavy Atoms26
    Rotatable Bonds7
    H-bond donors5
    H-bond Acceptors 7
    Cluster numberCluster75


    CHEMBL210966


    Show docking results

    Inhibition of:
    ASIC: 87 nM (ic50)
    Synonymous names
    CHEMBL210966
    CHEBI:452460
    SmilesCCCCCCN=C(N)NC(=O)C1=C(N=C(C(=N1)Cl)N)N
    11581093 
     
    16821771
    FormulaC12H20ClN7O
    Molweight313.786
    Heavy Atoms21
    Rotatable Bonds7
    H-bond donors4
    H-bond Acceptors 6
    Cluster numberCluster75


    CHEMBL377688


    Show docking results

    Inhibition of:
    ASIC: 107 nM (ic50)
    Synonymous names
    CHEMBL377688
    CHEBI:452493
    SmilesC(CO)N=C(N)NC(=O)C1=C(N=C(C(=N1)Cl)N)N
    11594744 
     
    16821771
    FormulaC8H12ClN7O2
    Molweight273.68
    Heavy Atoms18
    Rotatable Bonds4
    H-bond donors5
    H-bond Acceptors 7
    Cluster numberCluster75


    CHEMBL211773


    Show docking results

    Inhibition of:
    ASIC: 41 nM (ic50)
    Synonymous names
    CHEMBL211773
    CHEBI:452285
    SmilesCOC1=CC=C(C=C1)COCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N
    11603568 
     
    16821771
    FormulaC16H20ClN7O3
    Molweight393.828
    Heavy Atoms27
    Rotatable Bonds8
    H-bond donors4
    H-bond Acceptors 8
    Cluster numberNo cluster with more than 3 Compounds available


    CHEMBL377986


    Show docking results

    Inhibition of:
    ASIC: 15 nM (ic50)
    Synonymous names
    CHEMBL377986
    CHEBI:452540
    SmilesCOC1=CC=C(C=C1)CCCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N
    11604337 
     
    16821771
    FormulaC17H22ClN7O2
    Molweight391.855
    Heavy Atoms27
    Rotatable Bonds8
    H-bond donors4
    H-bond Acceptors 7
    Cluster numberCluster408


    CHEMBL213175


    Show docking results

    Inhibition of:
    ASIC: 51 nM (ic50)
    Synonymous names
    CHEMBL213175
    CHEBI:452614
    SmilesC1=CC(=CC=C1CCCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N)C(=O)O
    11611966 
     
    16821771
    FormulaC17H20ClN7O3
    Molweight405.839
    Heavy Atoms28
    Rotatable Bonds8
    H-bond donors5
    H-bond Acceptors 8
    Cluster numberCluster75


    CHEMBL380011


    Show docking results

    Inhibition of:
    ASIC: 20 nM (ic50)
    Synonymous names
    CHEMBL380011
    CHEBI:452357
    SmilesC1=CC(=CC(=C1)O)CCCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N
    11617778 
     
    16821771
    FormulaC16H20ClN7O2
    Molweight377.829
    Heavy Atoms26
    Rotatable Bonds7
    H-bond donors5
    H-bond Acceptors 7
    Cluster numberCluster75


    CHEMBL210981


    Show docking results

    Inhibition of:
    ASIC: 108 nM (ic50)
    Synonymous names
    CHEMBL210981
    CHEBI:452492
    SmilesCCCCCCCCN=C(N)NC(=O)C1=C(N=C(C(=N1)Cl)N)N
    11625053 
     
    16821771
    FormulaC14H24ClN7O
    Molweight341.84
    Heavy Atoms23
    Rotatable Bonds9
    H-bond donors4
    H-bond Acceptors 6
    Cluster numberCluster75


    CHEMBL211664


    Show docking results

    Inhibition of:
    ASIC: 50 nM (ic50)
    Synonymous names
    CHEMBL211664
    CHEBI:452518
    SmilesC1=CC=C(C=C1)CCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N
    11646675 
     
    16821771
    FormulaC15H18ClN7O
    Molweight347.803
    Heavy Atoms24
    Rotatable Bonds6
    H-bond donors4
    H-bond Acceptors 6
    Cluster numberCluster75


    CHEMBL212531


    Show docking results

    Inhibition of:
    ASIC: 7 nM (ic50)
    Synonymous names
    CHEMBL212531
    CHEBI:452580
    SmilesC1=CC(=CC=C1CCCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N)OCC(CO)O
    11656843 
     
    16821771
    FormulaC19H26ClN7O4
    Molweight451.907
    Heavy Atoms31
    Rotatable Bonds11
    H-bond donors6
    H-bond Acceptors 9
    Cluster numberCluster408


    CHEMBL377239


    Show docking results

    Inhibition of:
    ASIC: 68 nM (ic50)
    Synonymous names
    CHEMBL377239
    CHEBI:452355
    SmilesC1=CC=C(C=C1)CCCCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N
    11661541 
     
    16821771
    FormulaC17H22ClN7O
    Molweight375.856
    Heavy Atoms26
    Rotatable Bonds8
    H-bond donors4
    H-bond Acceptors 6
    Cluster numberCluster75


    CHEMBL211793


    Show docking results

    Inhibition of:
    ASIC: 88 nM (ic50)
    Synonymous names
    CHEMBL211793
    CHEBI:452434
    SmilesC1=CC(=CC=C1CCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N)O
    11703297 
     
    16821771
    FormulaC15H18ClN7O2
    Molweight363.802
    Heavy Atoms25
    Rotatable Bonds6
    H-bond donors5
    H-bond Acceptors 7
    Cluster numberCluster75


    CHEMBL211611


    Show docking results

    Inhibition of:
    ASIC: 66 nM (ic50)
    Synonymous names
    CHEMBL211611
    CHEBI:452517
    SmilesC1=CC=C(C=C1)CCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N
    11717656 
     
    16821771
    FormulaC14H16ClN7O
    Molweight333.776
    Heavy Atoms23
    Rotatable Bonds5
    H-bond donors4
    H-bond Acceptors 6
    Cluster numberCluster75


    CHEMBL210866


    Show docking results

    Inhibition of:
    ASIC: 477 nM (ic50)
    Synonymous names
    CHEMBL210866
    CHEBI:452394
    SmilesC1=CC=C(C=C1)CCCCCCCCN=C(N)NC(=O)C2=C(N=C(C(=N2)Cl)N)N
    11719431 
     
    16821771
    FormulaC20H28ClN7O
    Molweight417.936
    Heavy Atoms29
    Rotatable Bonds11
    H-bond donors4
    H-bond Acceptors 6
    Cluster numberCluster75


    ACMC-20ailv


    Show similar structuresShow docking results

    Inhibition of:
    Synonymous names
    ACMC-20ailv
    CTK1A1283
    W4639
    SureCN505055
    AC1Q2525
    A25880
    CHEMBL1770731
    AK-25184
    WTI-11588
    ANW-75041
    AM20050217
    CHEBI:1243035
    S14-1936
    AKOS013709659
    AG-E-65082
    6-Bromo-1,2,3,4-tetrahydroisoquinoline
    6-BROMO-1,2,3,4-TETRAHYDRO-ISOQUINOLINE
    226942-29-6
    MolPort-009-197-740
    6-BROMO-1,2,3,4-TETRA HYDRO ISO QUINOLINE
    Isoquinoline, 6-bromo-1,2,3,4-tetrahydro-
    Isoquinoline,6-bromo-;NSC 229320;6-Bromo-isoquinoline;
    SmilesC1CNCC2=C1C=C(C=C2)Br
    15885183 
     
    21257308
    FormulaC9H10BrN
    Molweight212.086
    Heavy Atoms11
    Rotatable Bonds0
    H-bond donors1
    H-bond Acceptors 1
    Cluster numberNo cluster with more than 3 Compounds available
    Vendors
    ABI Chem
    Achemica
    AK Scientific, Inc. (AKSCI)
    AKos Consulting & Solutions
    Amadis Chemical
    Angene Chemical
    Angene International
    Anward
    Apexmol
    Ark Pharm, Inc.
    Chembase.cn
    ChemFrog
    ChemMol
    IS Chemical Technology
    MolPort
    Oakwood Products


    Guanamprazine


    Show similar structuresShow docking results

    Inhibition of:
    ASIC3: 4400 nM (ic50)
     63000 nM (ic50)
    Metabolism
    Extrarenal fraction (Q0)Elimination half-life (EHL)
    0.259.6h
    Synonymous names
    Guanamprazin
    Amiprazidine
    Amiloride hydrochloride hydrate
    Guanamprazine
    Amipramizide
    Amipramizid
    Amipramidin
    Amiloridum
    Amilorida
    Amyloride
    Amiclaran
    AMILORIDE
    Midamor
    Amiloride HCL
    AMR
    AC1Q3POC
    Midamor (Hydrochloride dihydrate)
    Amikal (Hydrochloride dihydrate)
    CHEMBL945
    C6H8ClN7O
    1f5l
    AC1L27IZ
    U460
    Amiloride (INN)
    Amiclaran (TN)
    Amilorida [INN-Spanish]
    Amiloridum [INN-Latin]
    UNII-7DZO8EB0Z3
    Tocris-0890
    CID16231
    BIDD:GT0466
    Amiloride [INN:BAN]
    DB00594
    HMS1989O14
    HMS2213E05
    HMS1791O14
    D07447
    N-Amidino-3,5-diamino-6-chloropyrazinecarboxamide
    C06821
    CHEBI:2639
    HMS2089H05
    CCRIS 6545
    SBB037856
    ST079279
    LS-1094
    DAP000187
    Spectrum_000034
    N-Amidino-3,5-diamino-6-chlorpyrazincarboxamid
    BSPBio_000013
    KBioSS_000292
    AC-13631
    KBioGR_000544
    KBioGR_000292
    Lopac-A-7410
    CPD-10324
    BSPBio_001826
    DSSTox_GSID_43853
    BSPBio_001572
    KBioSS_000394
    Prestwick1_000007
    Spectrum4_000132
    SPBio_000136
    DSSTox_CID_23853
    Prestwick0_000007
    Spectrum3_000293
    ZINC04340269
    3,5-Diamino-N-(aminoiminomethyl)-6-chloropyrazinecarboxamide
    Spectrum2_000118
    Prestwick3_000007
    MK-870 (Hydrochloride dihydrate)
    Prestwick2_000007
    Spectrum5_000776
    SPBio_001934
    NINDS_000182
    DSSTox_RID_80077
    CCG-204206
    AB00053415
    KBio1_000182
    KBio2_005428
    Lopac0_000111
    KBio2_002962
    DivK1c_000182
    KBio3_001326
    KBio2_002860
    AKOS015961348
    KBio3_000584
    BPBio1_000015
    KBio2_000394
    KBio3_000583
    KBio2_000292
    KBio2_005530
    Bio1_000848
    BCBcMAP01_000101
    Bio1_000359
    IDI1_034042
    IDI1_000182
    Bio2_000772
    MLS000758249
    Bio2_000292
    MLS001060798
    Bio1_001337
    3,5-diamino-N-carbamimidoyl-6-chloropyrazine-2-carboxamide
    SMR000449325
    SMR000486264
    Tox21_110080
    NCGC00015089-01
    NCGC00024443-05
    NCGC00015089-03
    NCGC00015089-09
    NCGC00015089-16
    NCGC00024443-02
    NCGC00015089-07
    NCGC00015089-15
    NCGC00015089-12
    NCGC00024443-09
    NCGC00015089-06
    2609-46-3
    NCGC00015089-14
    NCGC00015089-08
    NCGC00024443-07
    NCGC00015089-05
    NCGC00015089-13
    NCGC00015089-02
    NCGC00024443-06
    NCGC00015089-04
    NCGC00015089-11
    3,5-diamino-6-chloro-N-(diaminomethylidene)pyrazine-2-carboxamide
    EINECS 220-024-7
    Pyrazinecarboxamide, 3,5-diamino-N-(aminoiminomethyl)-6-chloro-, monohydrochloride
    CAS-2609-46-3
    Pyrazinecarboxamide, 3,5-diamino-N-(aminoiminomethyl)-6-chloro-
    MolPort-005-937-651
    2016-88-8 (anhydrous hydrochloride)
    MolPort-005-934-472
    17440-83-4 (hydrochloride)
    117188-EP2298776A1
    117188-EP2277879A1
    3,5-diamino-N-[amino(imino)methyl]-6-chloropyrazine-2-carboxamide
    (3,5-diamino-6-chloropyrazin-2-yl)-N-(???methyl)carboxamide
    BRD-K97181089-310-03-0
    BRD-K97181089-003-02-3
    AMILORIDE (SEE ALSO: AMILORIDE HCL (2016-88-8))
    SmilesC1(=C(N=C(C(=N1)Cl)N)N)C(=O)N=C(N)N
    16231 
     
    19339181,
    FormulaC6H8ClN7O
    Molweight229.627
    Heavy Atoms15
    Rotatable Bonds1
    H-bond donors4
    H-bond Acceptors 5
    Cluster numberCluster695
    Vendors
    Abbott Labs
    ABI Chem
    AK Scientific, Inc. (AKSCI)
    AKos Consulting & Solutions
    Ambinter
    Chembase.cn
    ChemExper Chemical Directory
    ChemFrog
    ChemMol
    Hangzhou APIChem Technology
    TimTec
    ZINC


    CHEMBL1770744


    Show similar structuresShow docking results

    Inhibition of:
    ASIC3: 3300 nM (ic50)
    Synonymous names
    CHEMBL1770744
    CHEBI:1243048
    SmilesC1CNCC2=C1C=C(C=C2)C3=CC(=CC(=C3)Cl)Cl
    21473659 
     
    21257308
    FormulaC15H13Cl2N
    Molweight278.176
    Heavy Atoms18
    Rotatable Bonds1
    H-bond donors1
    H-bond Acceptors 1
    Cluster numberNo cluster with more than 3 Compounds available


    Acetylsalicylsaure


    Show docking results

    Inhibition of:
    ASIC3: 92000 nM (ic50)
    Metabolism
    Extrarenal fraction (Q0)Elimination half-life (EHL)
     3-4.5 h
    Synonymous names
    Azetylsalizylsaeure
    Acetylsalicylsaeure
    Acetylsalicylsaure
    Rheumintabletten
    Acetylsalicylate
    Kyselina acetylsalicylova
    Acetilsalicilico
    Acide acetylsalicylique
    Acidum acetylsalicylicum
    Cardioaspirina
    Enterosarein
    Acido acetilsalicilico
    Cardioaspirin
    Enterosarine
    Enterophen
    Triaminicin
    Acetoxybenzoic acid
    Aloxiprimum
    Acetilum acidulatum
    Acetosalin
    Acetylsalycilic acid
    ACETYLSALICYLIC ACID
    Bialpirinia
    Acetysalicylic acid
    Polopiryna
    Aspirdrops
    Bialpirina
    Acenterine
    Salcetogen
    Aceticyl
    Salacetin
    Bufferin
    Polopirin
    Aspergum
    Aspirine
    Premaspin
    Entericin
    Contrheuma retard
    Salospir
    Neuronika
    Acimetten
    Endosprin
    Acetylin
    Acetylsal
    Persistin
    Acylpyrin
    Pharmacin
    Clariprin
    Pravigard
    Colfarit
    Measurin
    Acetysal
    Magnecyl
    Acetisal
    Micristin
    Claradin
    Rheumin tabletten
    Acetosal
    Globentyl
    Kapsazal
    Acetophen
    Entrophen
    Benaspir
    Acetyonyl
    Temperal
    Istopirin
    o-Acetoxybenzoate
    Acetonyl
    Solpyron
    Delgesic
    Solupsan
    2-Acetoxybenzenecarboxylic acid
    Helicon
    Aspalon
    Acetard
    Toldex
    Endydol
    Solfrin
    Asatard
    Asteric
    Caprin
    Ecotrin
    Globoid
    Empirin
    Rhonal
    Medisyl
    Dispril
    Asagran
    Asacard
    Extren
    Ecolen
    Pirseal
    Acisal
    ZORprin
    Asprin
    Duramax
    Asaphen
    Easprin
    Levius
    Saletin
    Acesal
    Decaten
    Acetosalic acid
    Idragin
    Rhodine
    Solprin
    Tasprin
    aspirin
    Cemirit
    Novid
    Aspro
    Ronal
    XAXA
    Aspec
    o-Carboxyphenyl acetate
    component of Robaxisal
    Bayer Buffered
    O-Acetylsalicylic acid
    Adiro
    Supac
    component of Persistin
    Salicylic acid acetate
    O-accetylsalicylic acid
    component of Coricidin
    Yasta
    Bayer
    ASA
    Kyselina 2-acetoxybenzoova
    Solprin acid
    Aspro Clear
    component of Zactirin
    Empirin with Codeine
    ACETYLSALICYLIC ACID, ASPIRIN
    ECM
    AIN
    2-Acetoxybenzoate
    o-Acetoxybenzoic acid
    component of Synirin
    acetyl salicylic acid
    Aspir-Mox
    Acetylsalicylsaure [German]
    component of Midol
    Spira-Dine
    Bayer Plus
    2-acetyloxybenzoic acid
    Triple-sal
    2-Carboxyphenyl acetate
    Acetylsalicylsaure (GERMAN)
    Bi-prin
    CHEMBL25
    Nu-seals aspirin
    2-Acetoxybenzoic acid
    1oxr
    Nu-seals
    Salicylic acid, acetate
    Acido O-acetil-benzoico
    Kyselina acetylsalicylova [Czech]
    Acide acetylsalicylique (FRENCH)
    Acido acetilsalicilico [Italian]
    Acide acetylsalicylique [French]
    o-(Acetyloxy)benzoate
    O-Acetylsalicylic acid; Aspirin
    AC1L1D8U
    Aspirina 03
    AC1Q1LA0
    Bayer Extra Strength Aspirin for Migraine Pain
    St. Joseph
    Bayer Children's Aspirin
    UNII=R16CO5Y76E
    SureCN1353
    Ascoden-30
    8-hour Bayer
    Bayer Aspirin 8 Hour
    H740
    KSC269M6D
    o-(Acetyloxy)benzoic acid
    Dolean pH 8
    component of Ascodeen-30
    Aspalon (JAN)
    A.S.A
    CID2244
    ACMC-209kpz
    acide 2-(acetyloxy)benzoique
    PubChem20190
    St. Joseph Aspirin for Adults
    Kyselina 2-acetoxybenzoova [Czech]
    HMDB01879
    CTK1G9661
    HMS501L17
    HSDB 652
    Easprin (TN)
    2-(Acetyloxy)benzoic acid
    A5376_SIGMA
    SP 189
    component of St. Joseph Cold Tablets
    A3160_SIGMA
    NSC27223
    DB00945
    A2093_SIGMA
    LP00038
    BIDD:GT0118
    LS-143
    A6810_SIGMA
    Bay E4465
    SPECTRUM1500130
    Aspirin [BAN:JAN]
    WLN: QVR BOV1
    HMS2091K13
    D00109
    UNII R16CO5Y76E
    S-211
    DSSTox_CID_108
    HMS2090G03
    C01405
    HMS1920E13
    HMS3260G17
    UNII-R16CO5Y76E
    CCRIS 3243
    HMS2233L18
    DAP000843
    PL-2200
    STL137674
    SBB015069
    A.S.A.
    Bayer Enteric 500 mg Arthritis Strength
    NSC406186
    BBL005469
    AC 5230
    NSC755899
    A.S.A. empirin
    ST075414
    DAP001506
    Acido O-acetil-benzoico [Italian]
    nchem.859-comp6
    component of Darvon with A.S.A
    CHEBI:15365
    2-(AcetYl-Oxy)Benzoic Acid
    Spectrum_001245
    A 5376
    D001241
    Bayer Enteric 325 mg Regular Strength
    DSSTox_GSID_20108
    KB-47125
    KBioGR_002271
    CCG-39490
    KBioGR_000398
    NSC 27223
    ANW-31125
    Bayer Enteric 81 mg Adult Low Strength
    AB1003266
    NSC-27223
    Lopac-A-5376
    KBioSS_002272
    KBioSS_001725
    Spectrum5_000740
    NINDS_000555
    DSSTox_RID_75372
    Bay-e-4465
    SPBio_001838
    Spectrum4_000099
    Spectrum3_001295
    cMAP_000006
    Spectrum2_001899
    Aspirin (JP16/USP)
    Aspirin (JP15/USP)
    NSC-755899
    NSC-406186
    AI3-02956
    KBio2_002271
    Lopac0_000038
    KBio3_002149
    AKOS000118884
    Benzoicacid, 2-(acetyloxy)-
    KBio2_001725
    KBio2_007407
    KBio1_000555
    DivK1c_000555
    KBio2_006861
    I14-7505
    KBio2_004839
    KBio2_004293
    KBio3_002751
    BAY-1019036
    MLS001336046
    MLS001336045
    MLS001066332
    BRN 0779271
    MLS001055329
    AG-H-98095
    SMR000059138
    IDI1_000555
    EU-0100038
    AG-F-71040
    2-Acetoxybenzoic acid; O-Acetylsalicylic acid; ASA; Aspirin
    50-78-2
    R16CO5Y76E [UNII]
    Tox21_202117
    NCI60_002222
    Tox21_110076
    Tox21_300146
    Benzoic acid, 2-(acetyloxy)-
    CAS-50-78-2
    NCGC00090977-03
    NCGC00015067-05
    NCGC00015067-11
    NCGC00090977-02
    NCGC00090977-07
    NCGC00015067-03
    NCGC00015067-10
    NCGC00090977-01
    NCGC00090977-06
    NCGC00015067-02
    NCGC00015067-04
    2349-94-2
    NCGC00015067-08
    NCGC00015067-09
    NCGC00259666-01
    NCGC00090977-05
    NCGC00015067-07
    NCGC00015067-01
    NCGC00254034-01
    NCGC00090977-04
    NCGC00015067-06
    NCGC00015067-12
    UNM-0000306102
    EINECS 200-064-1
    98201-60-6
    26914-13-6
    Pharmakon1600-01500130
    11126-37-7
    11126-35-5
    6474-EP2298764A1
    1777-EP2305219A1
    1777-EP2311453A1
    1777-EP2277865A1
    6474-EP1441224A2
    MolPort-000-871-622
    1777-EP2292227A2
    6474-EP2298757A2
    1777-EP2298776A1
    1777-EP2308510A1
    1777-EP2275420A1
    1777-EP2371811A2
    1777-EP2281818A1
    6474-EP2277875A2
    1777-EP2298768A1
    1777-EP2305652A2
    1777-EP2272825A2
    1777-EP2316459A1
    1777-EP2281815A1
    6474-EP2277861A1
    1777-EP2298765A1
    1777-EP2305640A2
    6474-EP2314585A1
    1777-EP2269990A1
    1777-EP2314593A1
    1777-EP2281563A1
    6474-EP2275420A1
    1777-EP2298764A1
    6474-EP2298765A1
    1777-EP2269989A1
    1777-EP2305260A1
    1777-EP2314590A1
    1777-EP2280008A2
    6474-EP2272832A1
    1777-EP2295055A2
    24189-EP2314590A1
    24189-EP2295409A1
    170197-EP2275413A1
    186947-EP2272935A1
    186947-EP2270113A1
    170197-EP2287156A1
    4-10-00-00138 (Beilstein Handbook Reference)
    D41527A7-A9EB-472D-A7FC-312821130549
    Rhodine(7CI);Salicylic acid acetate (8CI);2-(Acetyloxy)benzoic acid;AC 5230;Acetophen;Acetysal;Acimetten;Acisal;Saletin;Solpyron;Supac;Temperal;Toldex;Trombyl;Yasta;o-(Acetyloxy)benzoic acid;Acetyl Sa
    InChI=1/C9H8O4/c1-6(10)13-8-5-3-2-4-7(8)9(11)12/h2-5H,1H3,(H,11,12
    SmilesCC(=O)OC1=CC=CC=C1C(=O)O
    2244 
     
    FormulaC9H8O4
    Molweight180.157
    Heavy Atoms13
    Rotatable Bonds3
    H-bond donors1
    H-bond Acceptors 4
    Cluster numberNo cluster with more than 3 Compounds available