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1. 3-iodo-2-propynyl 2,4,5-trichlorophenyl Ether
2. Halotex
3. Mycilan
1. 777-11-7
2. Halotex
3. Mycanden
4. Mycilan
5. Polik
6. M-1028 (meiji)
7. 1,2,4-trichloro-5-(3-iodoprop-2-ynoxy)benzene
8. M 1028
9. 3-iodo-2-propynyl 2,4,5-trichlorophenyl Ether
10. 2,4,5-trichlorophenyl Iodopropargyl Ether
11. Nsc-100071
12. Ether, 3-iodo-2-propynyl 2,4,5-trichlorophenyl
13. Haloprogina
14. Haloprogine
15. Aiu7053owl
16. Chembl1289
17. Benzene, 1,2,4-trichloro-5-((3-iodo-2-propynyl)oxy)-
18. Haloprogin (200 Mg)
19. Haloproginum
20. M-1028
21. Nsc100071
22. Haloprogine [inn-french]
23. Haloproginum [inn-latin]
24. Ncgc00181134-01
25. Haloprogina [inn-spanish]
26. 1,2,4-trichloro-5-((3-iodoprop-2-yn-1-yl)oxy)benzene
27. 1,2,4-trichloro-5-[(3-iodoprop-2-yn-1-yl)oxy]benzene
28. Benzene, 1,2,4-trichloro-5-[(3-iodo-2-propynyl)oxy]-
29. Halotex (tn)
30. Component Of Halotex
31. Einecs 212-286-6
32. 2,4,5-trichlorophenyl Gamma-iodopropargil Ether
33. 2,4,5-trichlorophenyl-gamma-iodopropargyl Ether
34. Unii-aiu7053owl
35. Nsc 100071
36. (3-iod-2-propinyl)-(2,4,5-trichlorphenyl)ether
37. Brn 1976771
38. Haloprogen
39. Haloprogin (jan/usan/inn)
40. Haloprogin [usan:usp:inn:jan]
41. Prestwick_232
42. Halotex (salt/mix)
43. Spectrum_001852
44. Haloprogin [mi]
45. Haloprogin [inn]
46. Haloprogin [jan]
47. Haloprogin [usan]
48. Haloprogin [vandf]
49. Ether,4,5-trichlorophenyl
50. Haloprogin [mart.]
51. Schembl3649
52. Haloprogin(200mg)
53. Dsstox_cid_26865
54. Dsstox_rid_81972
55. Haloprogin [who-dd]
56. Dsstox_gsid_46865
57. Kbioss_002369
58. 2,4,5-trichlorophenyl .gamma.-iodopropargyl Ether
59. Divk1c_000762
60. 1,2,4-trichloro-5-[(3-iodo-2-propynyl) Oxy]benzene
61. Chebi:5614
62. Benzene,1,2,4-trichloro-5-[(3-iodo-2-propynyl)oxy]
63. Dtxsid9046865
64. Haloprogin [orange Book]
65. Hms502g04
66. Kbio1_000762
67. Kbio2_002365
68. Kbio2_004933
69. Kbio2_007501
70. Wln: I1uu2or Bg Dg Eg
71. Ninds_000762
72. Hms3713a06
73. Bcp20218
74. Zinc1530649
75. Tox21_112741
76. Bdbm50194601
77. Ccg-220402
78. Db00793
79. 2,5-trichlorophenyl Iodopropargyl Ether
80. Idi1_000762
81. Ncgc00181134-02
82. Ncgc00181134-04
83. Cas-777-11-7
84. Hy-16246
85. Cs-0006262
86. 3-iodo-2-propynyl 2,5-trichlorophenyl Ether
87. D00339
88. 2,5-trichlorophenyl .gamma.-iodopropargil Ether
89. 2,5-trichlorophenyl .gamma.-iodopropargyl Ether
90. 777h117
91. 1,2,4-trichloro-5-(3-iodoprop-2-ynyloxy)benzene
92. Q5643439
93. 1,2,4-trichloro-5-(3-iodo-prop-2-ynyloxy)-benzene
94. Benzene,2,4-trichloro-5-[(3-iodo-2-propynyl)oxy]-
95. Brd-k13238168-001-01-2
Molecular Weight | 361.4 g/mol |
---|---|
Molecular Formula | C9H4Cl3IO |
XLogP3 | 4.6 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 1 |
Rotatable Bond Count | 2 |
Exact Mass | 359.83725 g/mol |
Monoisotopic Mass | 359.83725 g/mol |
Topological Polar Surface Area | 9.2 Ų |
Heavy Atom Count | 14 |
Formal Charge | 0 |
Complexity | 247 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
Used to treat fungal (Tinea) skin infections such as athlete's foot, jock itch, ringworm, and tinea versicolor.
Used as a topical ointment or cream in the treatment of Tinea infections. Tinea infections are superficial fungal infections caused by three species of fungi collectively known as dermatophytes (Trichophyton, Microsporum and Epidermophyton). Commonly these infections are named for the body part affected, including tinea corporis (general skin), tinea cruris (groin), and tinea pedis (feet).
Antifungal Agents
Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues. (See all compounds classified as Antifungal Agents.)
D - Dermatologicals
D01 - Antifungals for dermatological use
D01A - Antifungals for topical use
D01AE - Other antifungals for topical use
D01AE11 - Haloprogin
Haloprogin is a halogenated phenolic ether administered topically for dermotaphytic infections. The mechanism of action is unknown, but is thought to be via inhibition of oxygen uptake and disruption of yeast membrane structure and function. There is a higher incidence of cutaneous side effects with haloprogin, including irritation, burning, vesiculation (blisters), scaling, and itching. It is generally used when the infection is unresponsive to other antifungals.
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