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drugwars - npm Package Compare versions

Comparing version 0.1.10 to 0.1.11

83

lib/continents.json

@@ -1,56 +0,29 @@

[
{
"name":"North America",
"locations":[273,274,275,276,277,278,279,280
,281,282,283,284,285,286,287,288,289,290
,291,292,293,294,295,296,297,298,299,300
,301,302,303,304,305,306,307,308,309,310
,311,312,313,314,315,316,317,318,319,320
,321,322,323,324,325,326,327,328,329,330
,331,332,333,334,335,336,337,338,339,340
,341,342,343,344,345,346,347,348,349,350
,351,352,402]
},
{
"name":"South America",
"locations":[189,353,354,355,356,357,358,359
,360,361,362,363,364,365,366,367,368,369
,370,371,372,373,374,375,376,377,378,379
,380,381,382,383,384,385,386,387,388,389
,390,391,392,393,394,395,396,397,398,399
,400,401]
},
{
"name":"Europe",
"locations":[43,44,51,52,53,54,61,62,63,73,81
,83,84,85,86,88,89,279,326,452,453,454,458,459]
},
{
"name":"Asia",
"locations":[]
},
{
"name":"Africa",
"locations":[3,74,75,76,77,78,95,101,102,109,110,117,118,126,127,128,136,153,154,155,156,157,158,159,160
,161,162,163,164,165,166,167,168,169,170,171
,172,173,174,175,330,331,332,333,334,335,336
,337,338,339,340,341,342,343,344,417,418,419
,420,421,422,424,425,426,427,428,429,430,431
,432,433,434,435,436,437,438,439,440,441,442
,443,444,445,446,447,448,449,450,451,455,456,457]
},
{
"name":"Antarctica",
"locations":[176,177,178,179,180,181,182,183
,184,185,186,187,188,190,191,192,193,194
,195,196,197,198,199,200,201,202,203,204
,205,206,207,208,209,210,211,212]
},
{
"name":"Oceania",
"locations":[237,238,239,252,253,254,255,256
,257,258,259,260,261,262,263,264,265,266
,267,268,269,270,271,272]
}
[{
"name": "North America",
"locations": [273, 274, 275, 276, 277, 278, 279, 280, 281, 282, 283, 284, 285, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 296, 297, 298, 299, 300, 301, 302, 303, 304, 305, 306, 307, 308, 309, 310, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 322, 323, 324, 325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 352, 402]
},
{
"name": "South America",
"locations": [189, 353, 354, 355, 356, 357, 358, 359, 360, 361, 362, 363, 364, 365, 366, 367, 368, 369, 370, 371, 372, 373, 374, 375, 376, 377, 378, 379, 380, 381, 382, 383, 384, 385, 386, 387, 388, 389, 390, 391, 392, 393, 394, 395, 396, 397, 398, 399, 400, 401]
},
{
"name": "Europe",
"locations": [43, 44, 51, 52, 53, 54, 61, 62, 63, 73, 81, 83, 84, 85, 86, 88, 89, 279, 326, 452, 453, 454, 458, 459]
},
{
"name": "Asia",
"locations": []
},
{
"name": "Africa",
"locations": [3, 74, 75, 76, 77, 78, 95, 101, 102, 109, 110, 117, 118, 126, 127, 128, 136, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 330, 331, 332, 333, 334, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 417, 418, 419, 420, 421, 422, 424, 425, 426, 427, 428, 429, 430, 431, 432, 433, 434, 435, 436, 437, 438, 439, 440, 441, 442, 443, 444, 445, 446, 447, 448, 449, 450, 451, 455, 456, 457]
},
{
"name": "Antarctica",
"locations": [176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 210, 211, 212]
},
{
"name": "Oceania",
"locations": [237, 238, 239, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272]
}
]
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"description": "The opium poppy was cultivated in lower Mesopotamia as long ago as 3400 BCE. The chemical analysis of opium in the 19th century revealed that most of its activity could be ascribed to two alkaloids, codeine and morphine.\r\nDiamorphine was first synthesized in 1874 by C. R. Alder Wright, an English chemist working at St. Mary's Hospital Medical School in London. He had been experimenting with combining morphine with various acids. He boiled anhydrous morphine alkaloid with acetic anhydride for several hours and produced a more potent, acetylated form of morphine, now called diacetylmorphine or morphine diacetate.",
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"productname": "Cocaine",
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"id": "mdma",
"name": "MDMA",
"description": "MDMA was first synthesized in 1912 by Merck chemist Anton K�llisch. At the time, Merck was interested in developing substances that stopped abnormal bleeding. Merck wanted to avoid an existing patent held by Bayer for one such compound hydrastinine. K�llisch developed a preparation of a hydrastinine analogue, methylhydrastinine, at the request of fellow lab members, Walther Beckh and Otto Wolfes. MDMA (called methylsafrylamin, safrylmethylamin or N-Methyl-a-Methylhomopiperonylamin in Merck laboratory reports) was an intermediate compound in the synthesis of methylhydrastinine. Merck was not interested in MDMA itself at the time.On 24 December 1912, Merck filed two patent applications that described the synthesis and some chemical properties of MDMAand its subsequent conversion to methylhydrastinine.",
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"productname": "LSD",
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"name": "LSD",
"description": "LSD was first synthesized on November 16, 1938 by Swiss chemist Albert Hofmann at the Sandoz Laboratories in Basel, Switzerland as part of a large research program searching for medically useful ergot alkaloid derivatives. LSD's psychedelic properties were discovered 5 years later when Hofmann himself accidentally ingested an unknown quantity of the chemical. The first intentional ingestion of LSD occurred on April 19, 1943, when Hofmann ingested 250 �g of LSD. He said this would be a threshold dose based on the dosages of other ergot alkaloids. Hofmann found the effects to be much stronger than he anticipated. Sandoz Laboratories introduced LSD as a psychiatric drug in 1947.",
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"productname": "Anabolics",
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"id": "anabolics",
"name": "Anabolics",
"description": "The use of gonadal steroids pre-dates their identification and isolation. Medical use of testicle extract began in the late 19th century while its effects on strength were still being studied. The isolation of gonadal steroids can be traced back to 1931, when Adolf Butenandt, a chemist in Marburg, purified 15 milligrams of the male hormone androstenone from tens of thousands of litres of urine. This steroid was subsequently synthesized in 1934 by Leopold Ruzicka, a chemist in Zurich.In the 1930s, it was already known that the testes contain a more powerful androgen than androstenone, and three groups of scientists, funded by competing pharmaceutical companies in the Netherlands, Germany, and Switzerland, raced to isolate it. This hormone was first identified by Karoly Gyula David, E. Dingemanse, J. Freud and Ernst Laqueur in a May 1935 paper On Crystalline Male Hormone from Testicles (Testosterone). They named the hormone testosterone, from the stems of testicle and sterol, and the suffix of ketone. The chemical synthesis of testosterone was achieved in August that year, when Butenandt and G. Hanisch published a paper describing A Method for Preparing Testosterone from Cholesterol.",
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"productname": "Psilocybin",
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"id": "psylocybin",
"name": "Psilocybin",
"description": "There is evidence to suggest that psychoactive mushrooms have been used by humans in religious ceremonies for thousands of years. Murals dated 9000 to 7000 BCE found in the Sahara desert in southeast Algeria depict horned beings dressed as dancers, clothed in garb decorated with geometrical designs, and holding mushroom-like objects. Parallel lines extend from the mushroom shapes to the center of the dancers' heads. 6,000-year-old pictographs discovered near the Spanish town of Villar del Humo illustrate several mushrooms that have been tentatively identified as Psilocybe hispanica, a hallucinogenic species native to the area.",
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"name": "GHB",
"description": "Synthesis of the chemical GHB was first reported in 1874 by Alexander Zaytsev, but the first major research into its use in humans was conducted in the early 1960s by Dr. Henri Laborit to use in studying the neurotransmitter GABA. It quickly found a wide range of uses due to its minimal side-effects and short duration of action, the only difficulties being the narrow therapeutic dosage range and the dangers presented by its combination with alcohol and other nervous system depressants. GHB was widely used in France, Italy, and other European countries for several decades as a sleeping agent and an anesthetic in childbirth but problems with its abuse potential and development of newer drugs have led to a decrease in legitimate medical use of GHB in recent times. In the Netherlands, GHB could be bought as aphrodisiac and euphoriant in a smartshop for several years, until several incidents caused it to become regulated. The only common medical applications for GHB today are in the treatment of narcolepsy and more rarely alcoholism. In the typical scenario, GHB has been synthesized from ?-butyrolactone (GBL) by adding sodium hydroxide (lye) in ethanol or water.",
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"id": "ghb",
"name": "GHB",
"description": "Synthesis of the chemical GHB was first reported in 1874 by Alexander Zaytsev, but the first major research into its use in humans was conducted in the early 1960s by Dr. Henri Laborit to use in studying the neurotransmitter GABA. It quickly found a wide range of uses due to its minimal side-effects and short duration of action, the only difficulties being the narrow therapeutic dosage range and the dangers presented by its combination with alcohol and other nervous system depressants. GHB was widely used in France, Italy, and other European countries for several decades as a sleeping agent and an anesthetic in childbirth but problems with its abuse potential and development of newer drugs have led to a decrease in legitimate medical use of GHB in recent times. In the Netherlands, GHB could be bought as aphrodisiac and euphoriant in a smartshop for several years, until several incidents caused it to become regulated. The only common medical applications for GHB today are in the treatment of narcolepsy and more rarely alcoholism. In the typical scenario, GHB has been synthesized from ?-butyrolactone (GBL) by adding sodium hydroxide (lye) in ethanol or water.",
"icon": "ghb_icon.png",
"weight": 0,
"volume": 0
},
{
"drugmaxprice": 30,
"drugminprice": 10,
"drugmaxquantity": 0,
"drugeffect": null,
"productlocation":[],
"productid": 612,
"productname": "PCP",
"productdescription": "It is commonly mistakenly reported that PCP was first synthesized in 1926. This early synthesis, in fact, refers to the PCP intermediate PCC. PCP was actually discovered serendipitously by Victor Maddox, a chemist at Parke-Davis in Michigan, while investigating synthetic analgesic agents. Although unexpected, PCP was identified as potentially interesting, and as such, was submitted for pharmacological testing. The promising results of these pharmacological investigations led to the rapid development of PCP. It was approved for use as an investigational drug under the tradename Sernyl in the 1950s as an anesthetic, but because of its long half-life and adverse side effects, such as hallucinations, mania, delirium, and disorientation, it was removed from the market in 1965 and limited to veterinary use.",
"producttype": 0,
"producticon": "pcp_icon.png",
"productquantity": 0,
"productprice": 0,
"productweight": 0,
"productvolume": 0
"maxprice": 30,
"minprice": 10,
"effect": null,
"location":[],
"id": "pcp",
"name": "PCP",
"description": "It is commonly mistakenly reported that PCP was first synthesized in 1926. This early synthesis, in fact, refers to the PCP intermediate PCC. PCP was actually discovered serendipitously by Victor Maddox, a chemist at Parke-Davis in Michigan, while investigating synthetic analgesic agents. Although unexpected, PCP was identified as potentially interesting, and as such, was submitted for pharmacological testing. The promising results of these pharmacological investigations led to the rapid development of PCP. It was approved for use as an investigational drug under the tradename Sernyl in the 1950s as an anesthetic, but because of its long half-life and adverse side effects, such as hallucinations, mania, delirium, and disorientation, it was removed from the market in 1965 and limited to veterinary use.",
"icon": "pcp_icon.png",
"weight": 0,
"volume": 0
}
]

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