Substructure Search

8370

O=S(=O)(Nc1ccc2[nH]nc(-c3cc4ccccc4[nH]3)c2c1)c1ccccc1OC(F)(F)F
Reaction #53717
N-[3-(1H-indol-2-yl)-1H-indazol-5-yl]-2-trifluoromethoxy-benzenesulfonamide
Yield 58.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)ccc1S(=O)(=O)NCCCCCC(=O)O
Reaction #62610
ε(4-amino 2-methoxy-benzenesulfonamido) caproic acid
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1S(=O)(=O)NC1CCc2cc(Cn3cc(CO)c(C(F)(F)F)n3)ccc21
Reaction #71299
solid
Yield 28.1%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1cc(C(=O)O)cc(-n2cccc2)c1Oc1ccccc1
Reaction #75373
3-Sulphamoyl-4-phenoxy-5-[1-pyrrolyl]-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C)n1-c1cc(C(=O)O)cc(S(N)(=O)=O)c1Oc1ccccc1
Reaction #75376
3-Sulphamoyl-4-phenoxy-5-(2,5-dimethyl-1-pyrrolyl)-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)ccc1S(=O)(=O)NCCCCCC(=O)O
Reaction #93549
ε(4-amino 2-methoxy-benzenesulfonamido)caproic acid
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N2CCCCC2=O)cc(F)cc1S(=O)(=O)N[C@@H](Cc1cc(-c2ccc(Cl)s2)on1)C(=O)NCC1CC1
Reaction #163992
(S)-3-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-yl]-N-cyclopropylmethyl-2-[5-fluoro-2-methoxy-3-(2-oxo-piperidin-1-yl)-benzenesulfonylamino]-propionamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1OCCN[C@H](C)Cc1ccc(OC)c(S(N)(=O)=O)c1
Reaction #164436
Tamsulosin
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2C(=O)C(c3cc(CCN4CCCCC4)ccc3OC)(N3CC(O)CC3C(=O)N(C)C)c3cc(Cl)ccc32)c(OC(F)(F)F)c1
Reaction #176443
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)N2C(=O)C(c3cc(C)ccc3OC)(N3CC(OC(C)=O)CC3C(=O)N(C)C)c3cc(Cl)ccc32)c(OC(F)(F)F)c1
Reaction #177523
DOI: 10.1039/C8SC04228D
CCCCNS(=O)(=O)c1cc(C(=O)O)cc(NCc2ccccc2)c1Oc1ccccc1
Reaction #180031
DOI: 10.1039/C8SC04228D
CCN(CC)CCc1ccc(OC)c(C2(N3CC(O)CC3C(=O)N(C)C)C(=O)N(S(=O)(=O)c3ccc(OC)cc3OC(F)(F)F)c3ccc(Cl)cc32)c1
Reaction #180858
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCOc1cc(NS(=O)(=O)c2cc(N)ccc2OCCOC)c(O)cc1C
Reaction #182300
DOI: 10.1039/C8SC04228D
Nc1cc(S(=O)(=O)N2CCCCc3ccccc32)c(O)cc1Cl
Reaction #185005
DOI: 10.1039/C8SC04228D
Cl
Reaction #185580
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)CC(C#N)NS(=O)(=O)c1ccc(C(N)=O)cc1OCCc1cccc2ncccc12
Reaction #197565
DOI: 10.1039/C8SC04228D
COc1cc([N+](=O)[O-])ccc1S(=O)(=O)NC(C)(C)C
Reaction #198920
DOI: 10.1039/C8SC04228D
CNS(=O)(=O)c1c(Cl)ccc([N+](=O)[O-])c1O
Reaction #199780
DOI: 10.1039/C8SC04228D
CCC(Nc1c(Nc2ccc(Cl)c(S(=O)(=O)N(C)OC)c2O)c(=O)c1=O)C1CCC(C)O1
Reaction #201416
DOI: 10.1039/C8SC04228D
CCOCCNS(=O)(=O)c1c(Cl)ccc(N)c1O
Reaction #208102
DOI: 10.1039/C8SC04228D
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