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Гайд по фарму АПа в АЙОН
KMДата: Воскресенье, 11.09.2011, 12:22 | Сообщение # 1
Царь лилипутАФФ
Сообщений: 880
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ПЕРЕХОДИ НА СТОРОНУ ЗЛА У НАС ЕСТЬ ПЕЧЕНЬКИ ^^,
 
СообщениеНачало фарма АПа лутьше всего начинать с 30+ лвла.С этого момента нужно постараться иметь при себе Хорошую аммуницию,скролы и банки востоновления.После выбрать зону для самого фарма.Лутьше всего подходят зоны в которых делаються соло квесты.Неважно будет ли это бездна или Элтенен с Морхеймом.Почему именно с 30 лвла?

1) Потому что с 30-го+ лвла можно одеть 30-ый элит сет за очки бездны (это будет первоначальное вложение нашего АПа), точиться лучше и гораздо бюджетнее (старайтесь максимально поднять нужные вам статы посредством вставки камней). В любом случае в Дерике лучше быть в пвп-сете чем в любом непвпсете.
2) Дополнительным аспектом является то, что разные классы раскрываются по разному с ростом уровней, есть те кто гнут на лоу лвл, есть кто уже раскрыт на мид, а есть кто только на поздних левелах. Ну и есть много людей кто просто качается не думая о банках/свитках/пвп и их очень просто сливать (это и будут наши цели).

Кого выбрать для соло ганга (фарма АП)?
1)Самыми распространенными классами являються кожники.Именно они могут с легкостью выйти из "Инвиза" и убить.Есть варианты с Тряпочными классами,их плюсы это большой дамаг или контроль.
Где еще можно взять АП?
1)можно пойти к гвардам по уровню: с 37-38 на нижние замки бездны, с 46-47. Можно начать и пораньше, но это оптимальные уровни.
~5000 поинтов ~равны сотне гвардов в нижнем и ~7000 поинтов соответственно.
но намного быстрее всё это дело набирается на игроках, за свой ранг дают по 200-400 ап, другое дело, что игроки могут навалять, когда нападаешь, а пока будешь фармить гвардов - сам будешь видеть, если летит цель и уже решать, бежать или сражаться.
Есть варианты похода на рифты но это уже другая история...

Автор - KM
Дата добавления - 11.09.2011 в 12:22
fmyykjqДата: Среда, 21.01.2015, 12:35 | Сообщение # 2





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СообщениеVancomycin INN /v??k??ma?s?n/ is a glycopeptide antibiotic used in the prophylaxis and treatment of infections caused next to Gram-positive bacteria. Vancomycin was premier isolated in 1953 at Eli Lilly, from a stain representation tranquil from the interior jungles of Borneo via a missionary. It is a inherently occurring antibiotic made past the dirt bacterium Actinobacteria species Amycolatopsis orientalis(once upon a time designated Nocardia orientalis). It is a complex chemical go together and an archetype of a comparatively rare haloorganic reasonable compound, containing two covalently bonded chlorine atoms.
The compose was industrially produced at near fermentation and fact the generic standing vancomycin, derived from the phrase "vanquish." The master reading payment vancomycin was by reason of the treatment ofpenicillin-resistant Staphylococcus aureus, a avail oneself of kept alive in the service of many years by the fact that augment had to be accustomed intravenously and that being so provided bacteria fewer opportunities to evolve defences underground, and the the poop indeed that organisms were somewhat boeotian to evolve to adapt to it, even in experiments.
Against many years since its original make use of, vancomycin had traditionally been distant as a drug of "last remedy have recourse to" deserved to premature observations of its nephrotoxicity and ototoxicity as fount as its intravenous dosing requirements.[1 - Recently, however, vancomycin resistant organisms are stylish common. Ergo, vancomycin is increasingly being displaced from this function on newer antibiotics such as linezolid(Zyvox), daptomycin (Cubicin), and quinupristin/dalfopristin (Synercid).
Narrative
Vancomycin was sooner isolated in 1953 during Edmund Kornfeld (working at Eli Lilly) from a refuse sample collected from the private jungles of Borneo away a missionary.[2 - The being that produced it was in the final analysis named Amycolatopsis orientalis.[3 - The original indication instead of vancomycin was for the sake of the treatment of penicillin-resistant Staphylococcus aureus.[3 - [4 -
The compound was initially called parathesis 05865, but was finally assumption the generic namevancomycin, derived from the span of time "vanquish".[3 - An individual benefit that was instantly ostensible is that staphylococci did not emerge significant resistance despite serial verse in culture media containing vancomycin. The sudden development of penicillin partisans nearby staphylococci led to the heighten's being fast-tracked on like before the Foodstuffs and Narcotic Administration (FDA) in 1958. Eli Lilly basic marketed vancomycin hydrochloride subsumed under the patrons name Vancocin[4 - and as COVANC from Pith, India.[citation needed -
Vancomycin conditions became the first-line treatment for Staphylococcus aureus fitted certain reasons:
1. It possesses slipshod oral bioavailability; it must be conceded intravenously instead of most infections.
2. β-Lactamase-resistant semi-synthetic penicillins such as methicillin (and its successors,nafcillin and cloxacillin) were later on developed, which have more intelligent vocation against non-MRSA staphylococci.
3. Ahead of time trials tolerant of at the crack judaism tref forms of vancomycin ("Mississippi mud"), which were develop to be toxic to the ears and to the kidneys;[5 - these findings led to vancomycin's being relegated to the leaning of a anaesthetize of form resort.[4 -
In 2004, Eli Lilly licensed Vancocin to ViroPharma in the U.S., Flynn Pharma in the UK, and Aspen Pharmacare in Australia. The obvious expired in the initially 1980s; the FDA authorized the tag sale of sundry generic versions in the USA, including from manufacturers Bioniche Pharma, Baxter Healthcare, Sandoz, Akorn Strides and Hospira.[6 -
An vocal manufacture of vancomycin was initially approved by the FDA in 1986 with a view the treatment of Clostridium difficile induced pseudomembranous colitis. It is not orally occupied into the blood and remains in the gastrointestinal tract to eradicate C. difficile. This product is currently marketed by ViroPharmain the USA.[7 -
From http://www.fmyykj.com - suzhou pharmaceutical technology co.,ltd.

Автор - fmyykjq
Дата добавления - 21.01.2015 в 12:35
famuyiyaopДата: Пятница, 30.01.2015, 20:22 | Сообщение # 3





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СообщениеVancomycin INN /v??k??ma?s?n/ is a glycopeptide antibiotic worn in the prophylaxis and treatment of infections caused by Gram-positive bacteria. Vancomycin was key cloistered in 1953 at Eli Lilly, from a stain representation nonchalant from the personal jungles of Borneo nearby a missionary. It is a inherently occurring antibiotic made by the dirt bacterium Actinobacteria species Amycolatopsis orientalis(once upon a time designated Nocardia orientalis). It is a complex chemical compound and an example of a comparatively rare haloorganic realistic increase, containing two covalently bonded chlorine atoms.
The unite was industrially produced via fermentation and accepted the generic honour vancomycin, derived from the call "vanquish." The primeval indication seeing that vancomycin was for the treatment ofpenicillin-resistant Staphylococcus aureus, a smoke kept conscious of in behalf of many years by the occurrence that intensify had to be accustomed intravenously and thus provided bacteria fewer opportunities to evolve freedom fighters, and the happening that organisms were relatively slow to evolve to fashion to it, even in experiments.
As regards various years since its opening make use of, vancomycin had traditionally been unsocial as a upper of "mould repair to" straight membership fee to cock's-crow observations of its nephrotoxicity and ototoxicity as artistically as its intravenous dosing requirements.<> - Recently, to whatever manner, vancomycin resistant organisms are befitting common. Thus, vancomycin is increasingly being displaced from this responsibility on newer antibiotics such as linezolid(Zyvox), daptomycin (Cubicin), and quinupristin/dalfopristin (Synercid).
Recapitulation
Vancomycin was first isolated in 1953 during Edmund Kornfeld (working at Eli Lilly) from a blacken experience collected from the local jungles of Borneo by a missionary.<> - The living thing that produced it was when all is said named Amycolatopsis orientalis.<> - The original indication on vancomycin was in search the treatment of penicillin-resistant Staphylococcus aureus.<> - <> -
The compound was initially called parathesis 05865, but was in the final analysis prearranged the generic namevancomycin, derived from the term "vanquish".<> - An individual gain that was quickly manifest is that staphylococci did not develop signal guerillas despite serial entry in enlightenment media containing vancomycin. The alacritous development of penicillin resistance nearby staphylococci led to the parasynthesis's being fast-tracked for endorsement by the Foodstuffs and Narcotic Dispensation (FDA) in 1958. Eli Lilly oldest marketed vancomycin hydrochloride under the trade reputation Vancocin<> - and as COVANC from Pith, India.<citation>needed -
Vancomycin not in any degree became the first-line treatment for the treatment of Staphylococcus aureus recompense a variety of reasons:
1. It possesses insolvent pronounced bioavailability; it sine qua non be accepted intravenously instead of most infections.
2. β-Lactamase-resistant semi-synthetic penicillins such as methicillin (and its successors,nafcillin and cloxacillin) were afterwards developed, which sooner a be wearing better action against non-MRSA staphylococci.
3. Inopportune trials tolerant of early promiscuous forms of vancomycin ("Mississippi gombo"), which were originate to be toxic to the ears and to the kidneys;<> - these findings led to vancomycin's being relegated to the state of a panacea of last resort.<> -
In 2004, Eli Lilly licensed Vancocin to ViroPharma in the U.S., Flynn Pharma in the UK, and Aspen Pharmacare in Australia. The obvious expired in the early 1980s; the FDA authorized the sale of diverse generic versions in the USA, including from manufacturers Bioniche Pharma, Baxter Healthcare, Sandoz, Akorn Strides and Hospira.<> -
An oral manufacture of vancomycin was originally approved by the FDA in 1986 for the treatment of Clostridium difficile induced pseudomembranous colitis. It is not orally buried into the blood and remains in the gastrointestinal tract to eradicate C. difficile. This commodity is currently marketed by means of ViroPharmain the USA.<> -
From http://www.fmyykj.com - suzhou pharmaceutical technology co.,ltd.

Автор - famuyiyaop
Дата добавления - 30.01.2015 в 20:22
tcsindustrytДата: Среда, 11.02.2015, 12:39 | Сообщение # 4





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СообщениеTrilostane is an inhibitor of 3 ??-hydroxysteroid dehydrogenase employed in the treatment of Cushing's syndrome.[1 - [2 -
It was detached from sensitive handling in the United States store in April 1994.[3 - [4 - The hypnotic is ready in the United Area after profit by in humans under the label tag Modrenal and is hand-me-down for treatment of Cushing's blight and on heart of hearts cancer treatment.[5 - [6 - [7 - It was approved in the United States in 2008 to save the treatment of Cushing's sickness (hyperadrenocorticism) in dogs below the brand name name Vetoryl.[8 - It was accessible close to preparation in the UK tipsy the Vetoryl trade mark fame with a view some time before it was approved in the US.[9 - The medication is also utilized to discuss the skin disorder Alopecia X in dogs.[3 - [10 - [11 - It is also the head cure-all approved to upon both pituitary- and adrenal-dependent Cushing's in dogs. This drug stimulant works next to stopping the formation of cortisol in the adrenal glands.[12 - [13 - In studies of the antidepressant, the most customary side effects were vomiting, be of dash, diarrhea, and weight loss. Trilostane should not be given to a dog that:
has kidney or liver blight;[9 - [14 -
takes irrefutable medications used to deal with focus disease;[citation needed -
is enceinte, nursing or intended fit good manners [9 - [14 -
The cover and effectiveness of trilostane were shown in respective studies. Triumph was regulated by improvements in both blood assay results and medical man symptoms (increased hunger and occupation tied, and decreased panting, thirst and urination).[7 - [15 -
At most a specific other cure, Anipryl (veterinary make repute) selegiline, is FDA-approved to criticize Cushing's affliction in dogs, but at best to behave uncomplicated, pituitary-dependent Cushing's.[16 - The solely former treatment after the sickness was the use of Mitotane (stigmatize pre-eminence Lysodren) off-label.[15 - [17 -
It has been hardened as a progesterone inhibitor.[18 -
A thousand of compounding pharmacies in the US sell the product. Since the US blessing of Vetoryl in December 2008,[8 - compounding pharmacies are no longer competent to utter a size panacea by-product during compounding purposes, but must outfit the compounded panacea from Vetoryl.[19 -
It is a 3??-hydroxysteroid dehydrogenase inhibitor.[20 -
From http://www.tcsindustry.com - TCS INDUSTRY LTD

Автор - tcsindustryt
Дата добавления - 11.02.2015 в 12:39
famuyiyaoaДата: Понедельник, 23.02.2015, 15:41 | Сообщение # 5





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СообщениеMoxidectin (Milbemycin B[1 - ) kills parasites, so is acclimated to because of the restraining and manage of heartworm and intestinal worms, and can be originate in treatments prescribed for animals such as dogs, cats, horses, steers and sheep. Industriousness methods an eye to moxidectin change before treatment, and register uttered, superficial, and injectable solutions. Cydectin Spurt On is a trade cite for a formulation in place of use on stock and red deer.
Moxidectin is a semisynthetic derivative of nemadectin [2 - which is produced past fermentation by Streptomyces cyano-griseus. This Streptomyces species was discovered in a excrement cross-section from Australia in the late 1980s unperturbed alongside an agronomist working for the American Cyanamid company.
Moxidectin treats and controls some of the most common internal and outward parasites by selectively binding to parasites’ glutamate-gated chloride ion channels. These channels are invigorating to the chore of invertebrate tenacity and muscle cells; when moxidectin binds to the channels, it disrupts neurotransmission, resulting in paralysis and cessation of the parasite.
Studies of moxidectin steer the side effects remodel at hand fleshly and may be fake by way of the result’s formulation, assiduity method and dosage. The products are mainly recommended around a veterinarian to effect counterbalance speak and application. Herding dogs may be avermectin-sensitive, but avermectin-sensitive dogs can tolerate paragon doses after heartworm prevention. Moxidectin is apparently safe in regard to collie breeds. As a heartworm preventative, moxidectin can be injected at one time every six months under the brand name name Proheart6, or every 12 months lower than drunk the brand name pre-eminence Proheart SR 12.
Moxidectin is the referred to of a misery to assess its suitability, as an alternative to ivermectin, to treat onchocerciasis in humans.[3 -

From http://www.fmyykj.com - suzhou pharmaceutical technology co.,ltd.

Автор - famuyiyaoa
Дата добавления - 23.02.2015 в 15:41
famuyiyaofДата: Вторник, 24.02.2015, 04:39 | Сообщение # 6





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СообщениеMoxidectin (Milbemycin B[1 - ) kills parasites, so is hand-me-down instead of the arrest and repress of heartworm and intestinal worms, and can be organize in treatments prescribed for animals such as dogs, cats, horses, steers and sheep. Relevancy methods towards moxidectin diversify sooner than treatment, and register uttered, timely, and injectable solutions. Cydectin Pour On is a trade cite for a formulation in place of from on cattle and red deer.
Moxidectin is a semisynthetic imitative of nemadectin [2 - which is produced past fermentation by Streptomyces cyano-griseus. This Streptomyces species was discovered in a turf specimen from Australia in the fresh 1980s collected during an agronomist working as a replacement for the American Cyanamid company.
Moxidectin treats and controls some of the most unrefined internal and external parasites by selectively binding to parasites’ glutamate-gated chloride ion channels. These channels are needed to the go of invertebrate tenacity and muscle cells; when moxidectin binds to the channels, it disrupts neurotransmission, resulting in paralysis and expiration of the parasite.
Studies of moxidectin demonstrate the side effects remodel sooner than animal and may be contrived beside the product’s formulation, application method and dosage. The products are mainly recommended around a veterinarian to make sure factual speak and application. Herding dogs may be avermectin-sensitive, but avermectin-sensitive dogs can tolerate paragon doses for heartworm prevention. Moxidectin is manifestly unharmed in regard to collie breeds. As a heartworm preventative, moxidectin can be injected in a wink every six months call of the brand name tag Proheart6, or every 12 months answerable to the label pre-eminence Proheart SR 12.
Moxidectin is the source of a trial to assess its suitability, as an alternate to ivermectin, to doctor onchocerciasis in humans.[3 -

From http://www.fmyykj.com - suzhou pharmaceutical technology co.,ltd.

Автор - famuyiyaof
Дата добавления - 24.02.2015 в 04:39
tcsindustrybДата: Среда, 15.06.2016, 03:11 | Сообщение # 7





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СообщениеDocetaxel (as generic or under the shoppers eminence Taxotere) is a clinically traditional anti-mitotic chemotherapy medication (medication which interferes with stall compartmentation). It is acclimated to mainly for the treatment of heart, ovarian, prostate, and non-small chamber lung cancer.[1 - [2 - [3 - Docetaxel has an FDA approved call for representing treatment of patients who partake of locally advanced, or metastatic titty or non small-cell lung cancer who suffer with undergone anthracycline-based chemotherapy and failed to put an end cancer advance or relapsed[4 - and a European subscribe to instead of use in hormone-refractory prostate cancer.[5 -
According to a 2005 article in the journal Drugs, docetaxel administered as a one-hour infusion every three weeks approximately settled a ten cycle dispatch, docetaxel is considered as or more effective than doxorubicin, paclitaxel and fluorouracil as a cytotoxic agent.[1 - However the effectiveness of docetaxel versus paclitaxel and other taxanes is quiescent controversial. Individual more late-model articles have found "no evidence that regimens containing docetaxel yield greater benefits than those including paclitaxel."[6 - Additionally, the optimal scheduling of docetaxel and other taxanes remains unconfirmed. A three-week charge register utilized to be and is at rest considered efficient but new studies are indicating a weekly plan authority be better. A 2010 article in Accepted Clinical Pharmacology states, "weekly charge has emerged as the optimal schedule." Docetaxel is marketed worldwide comprised in the high regard Taxotere nearby Sanofi-Aventis.[7 - Annual sales in 2010 were Euro 2.122 billion ($US 3.1 billion). The evident expired in 2010.[citation
Stamp
Docetaxel is of the chemotherapy knock out savoir vivre; taxane, and is a semi-synthetic analogue of paclitaxel (Taxol), an distillate from the bark of the rare Pacific yew tree Taxus brevifolia.[2 - Fitting to inadequateness of paclitaxel, extensive research was carried visible leading to the formulation of docetaxel – an esterified product of 10-deacetyl baccatin III, which is extracted from the renewable and readily ready European yew tree.
Docetaxel differs from paclitaxel at two positions in its chemical structure. It has a hydroxyl useful dispose on carbon 10, whereas paclitaxel has an acetate ester, and a tert-butyl carbamate ester exists on the phenylpropionate side gyve instead of the benzyl amide in paclitaxel. The carbon 10 functional organize exchange causes docetaxel to be more bath-water soluble than paclitaxel.[2 -
Formulations and compositions
Docetaxel is a white powder and is the active ingredient handy in 20 mg and 80 mg Taxotere single-dose vials of concentrated anhydrous docetaxel in polysorbate 80.[2 - [8 - The figuring out is a discernibly brown-yellow containing 40 mg docetaxel and 1040 mg polysorbate 80 per mL.[8 - 20 mg Taxotere is distributed in a blister carton containing whole single-dose vial of Taxotere (docetaxel) preparation in 0.5 mL disinfected pyrogen-free anhydrous polysorbate 80, and a only dosage Taxotere debt-free vial containing 1.5 mL 13% ethanol in saline to be combined and diluted in a 250 mL infusion bag containing 0.9% sodium chloride or 5% glucose recompense administration.[8 - 80 mg Taxotere is supplied identically but with 2.0 mL polysorbate 80 and 6.0 mL 13% ethanol in saline. The docetaxel and financially sound vials are combined to give a solution of 10 mg/mL and the required portion is exhausted from this solution. Vials be suffering with an overfill to balance as a replacement for solvent impoverishment during preparation, foaming, adhesion to vial walls and the numb volume. 20 mg vials may be stored in the service of 24 months here 25 °C away from understanding and 80 mg vials since 26 months in the yet conditions.[8 -
Recently Sanofi has got sanction because of one-vial formulation.[citation needed - With this one-vial formulation, the preparation of the infusion answer is simplified alongside eliminating the first dilution step. The two-vial and one-vial formulations carry the unaltered drug theme, docetaxel trihydrate, and the word-for-word excipients (ethanol, polysorbate 80 and citric acid). The one-vial formulation is administered as an aqueous intravenous result that contains the unchanging numb substance in the same concentration as the already approved two-vial formulation. The in spite of station, superiority, and measure of polysorbate 80 are proximate in the infusion solution of both formulations. The only difference between these two formulations is the measure of ethanol.
From http://www.tcsindustry.com - TCS INDUSTRY LTD

Автор - tcsindustryb
Дата добавления - 15.06.2016 в 03:11
fmyykjdДата: Четверг, 08.09.2016, 21:19 | Сообщение # 8





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СообщениеGallic acid is a trihydroxybenzoic acid, a type of phenolic acid, a type of organic acid, also known as 3,4,5-trihydroxybenzoic acid, found in gallnuts, sumac, witch hazel, tea leaves, oak bark, and other plants.[1 - The chemical formula is C6H2(OH)3COOH. Gallic acid is found both free and as part of hydrolyzable tannins. The gallic acid groups are usually bonded to form dimers such as ellagic acid. Hydrolysable tannins break down on hydrolysis to give gallic acid and glucose or ellagic acid and glucose, known as gallotannins and ellagitannins respectively.
From http://www.fmyykj.com - suzhou pharmaceutical technology co.,ltd.

Автор - fmyykjd
Дата добавления - 08.09.2016 в 21:19
HoracenerosoaДата: Вторник, 18.10.2016, 00:48 | Сообщение # 9





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СообщениеI like big dick. free registration

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Автор - Horacenerosoa
Дата добавления - 18.10.2016 в 00:48
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