Chemokine receptor modulators and uses thereof

1. A compound having structural Formula (IIb):

or a pharmaceutically acceptable salt thereof, wherein:

z4 is 0, 1, or 2;

X 2 is CR 9 ;

n1, n2, n3.2, n3.3, n4, n7, and n9 are independently an integer from 0 to 4;

m1, m2, m3.2, m3.3, m4, m7, m9, v1, v2, v3.2, v3.3, v4, v7, and v9 are independently 1 or 2;

L 7 is a bond, —O—, —S—, —NR 7.2B —, —C(O)—, —C(O)O—, —S(O)—, —S(O) 2 —, R 41 -substituted or unsubstituted C 1 -C 8 alkylene or R 41 -substituted or unsubstituted C 3 -C 8 cycloalkylene;

R 41 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 42 -substituted or unsubstituted C 1 -C 8 alkyl, R 42 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 42 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 42 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 42 -substituted or unsubstituted C 6 -C 10 aryl, or R 42 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 42 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 43 -substituted or unsubstituted C 1 -C 8 alkyl, R 43 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 4 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 43 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 43 -substituted or unsubstituted C 6 -C 10 aryl, or R 43 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 43 is independently hydrogen, oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —Cl 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, unsubstituted C 1 -C 8 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycloalkyl, unsubstituted 3 to 8 membered heterocycloalkyl, unsubstituted C 6 -C 10 aryl, or unsubstituted 5 to 6 membered heteroaryl;

R 1 is hydrogen, halogen, —CX 1.1 3 , —CHX 1.1 2 , —CH 2 X 1.1 , —CN, —N 3 , —SO n1 R 1A —SO v1 NR 1B R 1C , —NHNR 1B R 1C , —ONR 1B R 1C , —NHC(O)NHNR 1B R 1C , —NHC(O)NR 1B R 1C , —N(O) m1 , —NR 1B R 1C , —C(O)R 1D , —C(O)OR 1D , —C(O)NR 1B R 1C , —OR 1A , —NR 1B SO 2 R 1A , —NR 1B C(O)R 1D , —NR 1B C(O)OR 1D , —NR 1B OR 1D , —OCX 1.1 3 , —OCHX 1.1 2 , —OCH 2 X 1.1 , R 11 -substituted or unsubstituted C 1 -C 8 alkyl, R 11 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 11 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 11 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 11 -substituted or unsubstituted C 6 -C 10 aryl, or R 11 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 11 is is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 12 -substituted or unsubstituted C 1 -C 8 alkyl, R 12 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 12 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 12 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 12 -substituted or unsubstituted C 6 -C 10 aryl, or R 12 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 12 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 13 -substituted or unsubstituted C 1 -C 8 alkyl, R 13 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 13 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 13 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 13 -substituted or unsubstituted C 6 -C 10 aryl, or R 13 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 13 is independently hydrogen, oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, unsubstituted C 1 -C 8 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycloalkyl, unsubstituted 3 to 8 membered heterocycloalkyl, unsubstituted C 6 -C 10 aryl, or unsubstituted 5 to 6 membered heteroaryl;

R 2 is hydrogen, halogen, —CX 2.1 3 , —CHX 2.1 2 , —CH 2 X 2.1 , —CN, —N 3 , —SO n2 R 2A , —SO v2 NR 2B R 2C , —NHR 2B R 2C , —ONR 2B R 2C , —NHC(O)NHNR 2B R 2C , —NHC(O)NR 2B R 2C , —N(O) m2 , —NR 2B R 2C , —C(O)R 2D , —C(O)OR 2D , —C(O)NR 2B R 2C , —OR 2A , —NR 2B SO 2 R 2A , —NR 2B C(O)R 2D , —NR 2B C(O)OR 2D , —NR 2B OR 2D , —OCX 2.1 3 , —OCHX 2.1 2 , —OCH 2 X 2.1 , R 14 -substituted or unsubstituted C 1 -C 8 alkyl, R 14 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 14 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 14 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 14 -substituted or unsubstituted C 6 -C 10 aryl, or R 14 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 14 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 15 -substituted or unsubstituted C 1 -C 8 alkyl, R 15 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 15 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 15 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 15 -substituted or unsubstituted C 6 -C 10 aryl, or R 15 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 15 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 16 -substituted or unsubstituted C 1 -C 8 alkyl, R 16 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 16 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 16 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 16 -substituted or unsubstituted C 6 -C 10 aryl, or R 16 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 16 is independently hydrogen, oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, unsubstituted C 1 -C 8 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycloalkyl, unsubstituted 3 to 8 membered heterocycloalkyl, unsubstituted C 6 -C 10 aryl, or unsubstituted 5 to 6 membered heteroaryl;

R 3.2 is hydrogen, halogen or —SO n3.2 R 3.2A ;

R 3.3 is hydrogen, halogen, or —SO n3.2 R 3.3A ;

R 4 is hydrogen, halogen, —CX 4.1 3 , —CHX 4.1 2 , —CH 2 X 4.1 , —CN, —N 3 , —SO n4 R 4A , —SO v4 NR 4B R 4C , —NHR 4B R 4C , —ONR 4B R 4C , —NHC(O)NHNR 4B R 4C , —NHC(O)NR 4B R 4C , —N(O) m4 , —NR 4B R 4C , —C(O)R 4D , —C(O)OR 4D , —C(O)NR 4B R 4C , —OR 4A , —NR 4B SO 2 R 4A , —NR 4B C(O)R 4D , —NR 4B C(O)OR 4D , —NR 4B OR 4D , —OCX 4.1 3 , —OCHX 4.1 2 , —OCH 2 X 4.1 , R 20 -substituted or unsubstituted C 1 -C 8 alkyl, R 20 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 20 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 20 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 20 -substituted or unsubstituted C 6 -C 10 aryl, or R 20 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 20 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 21 -substituted or unsubstituted C 1 -C 8 alkyl, R 21 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 21 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 21 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 21 -substituted or unsubstituted C 6 -C 10 aryl, or R 21 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 21 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 22 -substituted or unsubstituted C 1 -C 8 alkyl, R 22 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 22 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 22 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 22 -substituted or unsubstituted C 6 -C 10 aryl, or R 22 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 22 is independently hydrogen, oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, unsubstituted C 1 -C 8 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycloalkyl, unsubstituted 3 to 8 membered heterocycloalkyl, unsubstituted C 6 -C 10 aryl, or unsubstituted 5 to 6 membered heteroaryl;

R 7 is hydrogen, halogen, —CX 7.1 3 , —CHX 7.1 2 , —CH 2 X 7.1 , —CN, —N 3 , —SO n7 R 7A , —SO v7 NR 7B R 7C , —NR 7B R 7C , —ONR 7B R 7C , —NHC(O)NHNR 7B R 7C , —NHC(O)NR 7B R 7C , —N(O) m7 , —NR 7B R 7C , —C(O)R 7D , —C(O)OR 7D , —C(O)NR 7B R 7C , —OR 7A , —NR 7B SO 2 R 7A , —NR 7B C(O)R 7D , —NR 7B C(O)OR 7D , —NR 7B OR 7D , —OCX 7.1 3 , —OCHX 7.1 2 , —OCH 2 X 7.1 , R 29 -substituted or unsubstituted C1-C 8 alkyl, R 29 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 29 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 29 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 29 -substituted or unsubstituted C 6 -C 10 aryl, or R 29 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 29 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 30 -substituted or unsubstituted C 3 -C 8 alkyl, R 30 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 30 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 30 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 30 -substituted or unsubstituted C 6 -C 10 aryl, or R 30 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 30 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I—OCH 2 F, R 31 -substituted or unsubstituted C 1 -C 8 alkyl, R 31 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 31 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 31 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 31 -substituted or unsubstituted C 6 -C 10 aryl, or R 31 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 31 is independently hydrogen, oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, unsubstituted C 1 -C 8 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycloalkyl, unsubstituted 3 to 8 membered heterocycloalkyl, unsubstituted C 6 -C 10 aryl, or unsubstituted 5 to 6 membered heteroaryl;

R 9 is hydrogen, halogen, —CX 9.1 3 , —CHX 9.1 2 , —CH 2 X 9.1 , —CN, —N 3 , —SO n9 R 9A , —SO v9 NR 9B R 9C , —NHNR 9B R 9C , —ONR 9B R 9C , —NHC(O)NHNR 9B R 9C , —NHC(O)NR 9B R 9C , —N(O) m9 , —NR 9B R 9C , —C(O)R 9D , —C(O)OR 9D , —C(O)NR 9B R 9C , —OR 9A , —NR 9B SO 2 R 9A , —NR 9B C(O)R 9D , —NR 9B C(O)OR 9D , —NR 9B OR 9D , —OCX 9.1 3 , —OCHX 9.1 2 , —OCH 2 X 9.1 , R 35 -substituted or unsubstituted C 1 -C 8 alkyl, R 35 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 35 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 35 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 35 -substituted or unsubstituted C 6 -C 10 aryl, or R 35 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 35 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 36 -substituted or unsubstituted C 1 -C 8 alkyl, R 36 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 36 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 36 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 36 -substituted or unsubstituted C 6 -C 10 aryl, or R 36 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 36 is independently oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, R 37 -substituted or unsubstituted C 1 -C 8 alkyl, R 37 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 37 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 37 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 37 -substituted or unsubstituted C 6 -C 10 aryl, or R 37 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 37 is independently hydrogen, oxo, halogen, —CCl 3 , —CBr 3 , —CF 3 , —CI 3 , —CN, —OH, —NH 2 , —COOH, —CONH 2 , —NO 2 , —SH, —SO 3 H, —SO 4 H, —SO 2 NH 2 , —NHNH 2 , —ONH 2 , —NHC(O)NHNH 2 , —NHC(O)NH 2 , —NHSO 2 H, —NHC(O)H, —NHC(O)OH, —NHOH, —OCCl 3 , —OCF 3 , —OCBr 3 , —OCI 3 , —OCHCl 2 , —OCHBr 2 , —OCHI 2 , —OCHF 2 , —OCH 2 Cl, —OCH 2 Br, —OCH 2 I, —OCH 2 F, unsubstituted C 1 -C 8 alkyl, unsubstituted 2 to 8 membered heteroalkyl, unsubstituted C 3 -C 8 cycloalkyl, unsubstituted 3 to 8 membered heterocycloalkyl, unsubstituted C 6 -C 10 aryl, or unsubstituted 5 to 6 membered heteroaryl;

R 44 is hydrogen;

R 1A , R 1B , R 1C , R 1D , R 3.2A , R 3.3A , and R 7.2B are independently hydrogen, halogen, —CF 3 , —CCl 3 , —CBr 3 , —CI 3 , —COOH, —CONH 2 , R 11 -substituted or unsubstituted C 1 -C 8 alkyl, R 11 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 11 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 11 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 11 -substituted or unsubstituted C 6 -C 10 aryl, or R 11 -substituted or unsubstituted 5 to 6 membered heteroaryl; R 1B and R 1C substituents bonded to the same nitrogen atom may optionally be joined to form a R 11 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl or R 11 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 2A , R 2B , R 2C , and R 2D are independently hydrogen, halogen, —CF 3 , —CCl 3 , —CBr 3 , —CI 3 , —COOH, —CONH 2 , R 14 -substituted or unsubstituted C 1 -C 8 alkyl, R 14 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 14 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 14 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 14 -substituted or unsubstituted C 6 -C 10 aryl, or R 14 -substituted or unsubstituted 5 to 6 membered heteroaryl; R 2B and R 2C substituents bonded to the same nitrogen atom may optionally be joined to form a R14-substituted or unsubstituted 3 to 8 membered heterocycloalkyl or R 14 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 4A , R 4B , R 4C , and R 4D are independently hydrogen, halogen, —CF 3 , —CCl 3 , —CBr 3 , —CI 3 , —COOH, —CONH 2 , R 20 -substituted or unsubstituted C 1 -C 8 alkyl, R 20 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 20 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 20 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 20 -substituted or unsubstituted C 6 -C 10 aryl, or R 20 -substituted or unsubstituted 5 to 10 membered heteroaryl; R 4B and R 4C substituents bonded to the same nitrogen atom may optionally be joined to form a R 20 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl or R 20 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 7A , R 7B , R 7C , and R 7D are independently hydrogen, halogen, —CF 3 , —CCl 3 , —CBr 3 , —CI 3 , —COOH, —CONH 2 , R 29 -substituted or unsubstituted C 1 -C 8 alkyl, R 29 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 29 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 29 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 29 -substituted or unsubstituted C 6 -C 10 aryl, or R 29 -substituted or unsubstituted 5 to 6 membered heteroaryl; R 7B and R 7C substituents bonded to the same nitrogen atom may optionally be joined to form a R 29 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl or R 29 -substituted or unsubstituted 5 to 6 membered heteroaryl;

R 9A , R 9B , R 9C , and R 9D are independently hydrogen, halogen, —CF 3 , —CCl 3 , —CBr 3 , —CI 3 , —COOH, —CONH 2 , R 35 -substituted or unsubstituted C 1 -C 8 alkyl, R 35 -substituted or unsubstituted 2 to 8 membered heteroalkyl, R 35 -substituted or unsubstituted C 3 -C 8 cycloalkyl, R 35 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl, R 35 -substituted or unsubstituted C 6 -C 10 aryl, or R 35 -substituted or unsubstituted 5 to 6 membered heteroaryl; R 9B and R 9C substituents bonded to the same nitrogen atom may optionally be joined to form a R 35 -substituted or unsubstituted 3 to 8 membered heterocycloalkyl or R 35 -substituted or unsubstituted 5 to 6 membered heteroaryl;

and

X 1.1 , X 2.1 , X 4.1 , X 7.1 , and X 9.1 are independently —Cl, —Br, —I or —F,

wherein:

each substituted or unsubstituted 2 to 8 membered heteroalkyl contains at least one carbon atom and at least one heteroatom;

each substituted or unsubstituted 3 to 8 membered heterocycloalkyl contains at least one carbon atom and at least one heteroatom;

each substituted or unsubstituted 5 to 6 membered heteroaryl contains at least one carbon atom and at least one heteroatom;

each substituted or unsubstituted 2 to 8 membered heteroalkyl or substituted or unsubstituted 3 to 8 membered heterocycloalkyl contains at least one heteroatom selected from oxygen (O), nitrogen (N), sulfur (S), phosphorus (P), and silicon (Si); and

each substituted or unsubstituted 5 to 6 membered heteroaryl contains at least one heteroatom selected from oxygen (O), nitrogen (N), and sulfur (S).

2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 9 is hydrogen, —CF 3 , or unsubstituted methyl.

3. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the compound has structural Formula (IId):

4. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 4 is hydrogen, halogen, —CX 4.1 3 , —CHX 4.1 2 , —CH 2 X 4.1 , —CN, —NR 4B R 4C , —C(O)R 4D , —C(O)OR 4D , —C(O)NR 4B R 4C , —OR 4A , —NR 4B C(O)R 4D , —NR 4B C(O)OR 4D , —OCX 4.1 3 , —OCHX 4.1 2 , —OCH 2 X 4.1 , substituted or unsubstituted alkyl, or substituted or unsubstituted heteroalkyl.

5. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 4 is hydrogen, halogen, —CX 4.1 3 , —CHX 4.1 2 , —CH 2 X 4.1 , —CN, —C(O)OR 4D , —C(O)NR 4B R 4C , substituted or unsubstituted C 1 -C 4 alkyl, or substituted or unsubstituted 2 to 4 membered heteroalkyl.

6. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 4 is —Cl, —Br, —F, —CN, —COOH, —C(O)OCH 2 CH 3 , —C(CH 3 ) 2 OH, —C(O)NH 2 , —CF 3 , or —CH 3 .

7. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1 and R 2 are independently hydrogen, substituted or unsubstituted alkyl or substituted or unsubstituted heteroalkyl.

8. The compound of claim 7 , or a pharmaceutically acceptable salt thereof, wherein R 1 is substituted or unsubstituted alkyl.

9. The compound of claim 8 , or a pharmaceutically acceptable salt thereof, wherein R 1 is —CH 3 .

10. The compound of claim 7 , or a pharmaceutically acceptable salt thereof, wherein R 1 is hydrogen.

11. The compound of claim 7 , or a pharmaceutically acceptable salt thereof, wherein R 2 is substituted or unsubstituted alkyl.

12. The compound of claim 11 , or a pharmaceutically acceptable salt thereof, wherein R 2 is —CH 3 .

13. The compound of claim 7 , or a pharmaceutically acceptable salt thereof, wherein R 2 is hydrogen.

14. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 3.2 and R 3.3 are independently halogen.

15. The compound of claim 14 , or a pharmaceutically acceptable salt thereof, wherein R 3.2 and R 3.3 are independently chlorine.

16. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein L 7 is a bond, substituted or unsubstituted alkylene, or substituted or unsubstituted cycloalkylene.

17. The compound of claim 16 , or a pharmaceutically acceptable salt thereof, wherein L 7 is a substituted or unsubstituted C 4 -C 6 cycloalkylene.

18. The compound of claim 17 , or a pharmaceutically acceptable salt thereof, wherein L 7 is an unsubstituted C 4 -C 6 cycloalkylene.

19. The compound of claim 18 , or a pharmaceutically acceptable salt thereof, wherein L 7 is a substituted or unsubstituted cyclobutylene.

20. The compound of claim 16 , or a pharmaceutically acceptable salt thereof, wherein L 7 is a substituted or unsubstituted alkylene.

21. The compound of claim 20 , or a pharmaceutically acceptable salt thereof, wherein L 7 is a substituted or unsubstituted C 1 -C 6 alkylene.

22. The compound of claim 16 , or a pharmaceutically acceptable salt thereof, wherein L 7 is a bond.

23. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 7 is hydrogen, halogen, —SO n7 R 7A , —SO v7 NR 7B R 7C , —NHC(O)NR 7B R 7C , —NR 7B R 7C , —C(O)R 7D , —C(O)OR 7D , —C(O)NR 7B R 7C , —OR 7A , —NR 7B SO 2 R 7A , —NR 7B C(O)R 7D , —NR 7B C(O)OR 7D , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl or substituted or unsubstituted heteroaryl.

24. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 7 is —OR 7A , —C(O)R 7D , —C(O)OR 7D , —C(O)NR 7B R 7C , —SO n7 R 7A , —SO v7 NR 7B R 7C , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl or substituted or unsubstituted heteroaryl.

25. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 7 is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted phenyl, —C(O)OH, —C(O)OCH 3 , —C(O)OCH 2 CH 3 , —CH 2 C(O)OH, —NHC(O)OH, —NHC(O)OCH 3 , —NHC(O)OCH 2 CH 3 , —CH 2 C(O)OH, —CH 2 C(O)OCH 3 , —CH 2 C(O)OCH 2 CH 3 , —SO 2 CH 3 , —SO 2 CH 2 CH 3 , —SO 2 CH(CH 3 ) 2 , —NHSO 2 CH 3 , —NHSO 2 CH 2 CH 3 , —NHSO 2 CH(CH 3 ) 2 , —SO 2 NH 2 , —SO 2 NHCH 3 , —F, —OH, —CH 2 OH, —(CH 2 ) 2 OH, —(CH 2 ) 3 OH, —C(CH 3 ) 2 OH, —CH 2 SO 2 NH 2 , —(CH 2 ) 2 SO 2 NH 2 , —CH 2 C(O)NH 2 , —(CH 2 ) 2 C(O)NH 2 , —(CH 2 ) 3 C(O)NH 2 , —CH 2 NHSO 2 CF 3 , —(CH 2 ) 2 NHSO 2 CF 3 , —(CH 2 ) 3 NHSO 2 CF 3 , —CH 2 NHSO 2 CH 3 , —(CH 2 ) 2 NHSO 2 CH 3 , —(CH 2 ) 3 NHSO 2 CH 3 , —CH 2 SO 2 CH 3 , —(CH 2 ) 2 SO 2 CH 3 , —CH 2 SO 2 NH 2 , or —(CH 2 ) 2 SO 2 NH 2 .

26. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 7 is hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted phenyl, —C(O)OH, —C(O)OCH 3 , —C(O)OCH 2 CH 3 , —CH 2 C(O)OH, —NHC(O)OH, —NHC(O)OCH 3 , —NHC(O)OCH 2 CH 3 , —CH 2 C(O)OH, —CH 2 C(O)OCH 3 , —CH 2 C(O)OCH 2 CH 3 , —SO 2 CH 3 , —SO 2 CH 2 CH 3 , —SO 2 CH(CH 3 ) 2 , —NHSO 2 CH 3 , —NHSO 2 CH 2 CH 3 , —NHSO 2 CH(CH 3 ) 2 , —SO 2 NH 2 , —SO 2 NHCH 3 , —(CH 2 ) 2 OH, —CH 2 C(CH 3 ) 2 OH, —(CH 2 ) 3 OH, —(CH 2 ) 2 CH(CH 3 ) 2 OH, —(CH 2 ) 2 SO 2 NH 2 , —(CH 2 ) 3 SO 2 NH 2 , —(CH 2 ) 2 CONH 2 , —(CH 2 ) 3 CONH 2 —(CH 2 ) 3 CON(H)Me, —(CH 2 ) 3 CON(Me) 2 , —(CH 2 ) 2 SO 2 Me, —(CH 2 ) 3 SO 2 Me, —CH 2 CH(OH)Me, —CH 2 CO 2 H, —(CH 2 ) 2 CO 2 H, —CH(CH 3 )CH 2 CO 2 H, —(CH 2 ) 3 CO 2 H, —(CH 2 ) 2 SO 2 NHCH 3 , —(CH 2 ) 2 SO 2 N(CH 3 ) 2 , —(CH 2 ) 2 SO 2 —(N- morpholinyl), —(CH 2 ) 2 NHCOCH 3 , —(CH 2 ) 3 NHCOCH 3 , —(CH 2 ) 2 NHCOCH(CH 3 ) 2 , —(CH 2 ) 2 NHSO 2 CH 3 , —(CH 2 ) 2 NHSO 2 CF 3 , —(CH 2 ) 2 NHSO 2 NHCH(CH 3 ) 2 , —CH 2 CH(CH 3 )CH 2 OH (R and S), —CH(CH 3 )(CH 2 ) 2 OH, —CH 2 -(2-imidazoyl), —CH 2 -(4-imidazoyl), —CH 2 -(3-pyrazoyl), 4-tetrahydropyranyl, 3-oxetanyl, —(CH 2 ) 2 NHCO 2 Me, —(CH 2 ) 3 NHCO 2 Me, —CH 2 OH,

27. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein -L 7 -R 7 is carboxylic acid substituted cyclobutyl, carboxylic acid substituted cyclopentyl, or hydroxyl substituted ethyl; all optionally further substituted with substituted or unsubstituted alkyl.

28. A pharmaceutical composition comprising a pharmaceutically acceptable excipient and a compound of claim 1 , or a pharmaceutically acceptable salt thereof.