항암활성을 갖는 J 300 동충하초 추출물 및 이를함유하는 약제학적 조성물
    11.
    发明公开
    항암활성을 갖는 J 300 동충하초 추출물 및 이를함유하는 약제학적 조성물 有权
    提取物 具有抗菌活性的J300和含有其的药物组合物

    公开(公告)号:KR1020040012399A

    公开(公告)日:2004-02-11

    申请号:KR1020020045969

    申请日:2002-08-03

    Abstract: PURPOSE: Provided are an extract of Paecilomyces sp. J300 having antitumor activity and a pharmaceutical composition containing the same. The extract contains novel antitumor matters, and is thus useful for an antitumor drug composition. CONSTITUTION: A extract of Paecilomyces sp. J300 having antitumor activity contains, as antitumor matters, 5,3-dihydroxy-1-N-methyl-indoline-2-carbonylamino-alanyl-hydoxyisoleucinyl-glycine represented by the formula(1) or its derivatives. An antitumor drug composition contains one of 5,3-dihydroxy-1-N-methyl-indoline-2-carbonylamino-alanyl-hydoxyisoleucinyl-glycine or its derivatives including 5 alpha, 6 alpha-epoxy-(22E,24R)-ergosta-8(14), 22-diene-3 beta, 7 alpha-diol of the formula(2), 5 alpha, 6 alpha-epoxy-(22E, 24R)-ergosta-8, 22-diene-3 beta, 7 alpha-diol of the formula(3), ergosta-4, 6, 8(14), 22-tetraene-3-one of the formula(4) and 3 beta, 5 alpha-dihydroxy-6 beta-methoxyergosta-7, 22-diene of the formula(5).

    Abstract translation: 目的:提供拟青霉菌属 J300具有抗肿瘤活性和含有其的药物组合物。 提取物含有新的抗肿瘤物质,因此可用于抗肿瘤药物组合物。 构成:拟青霉菌提取物 具有抗肿瘤活性的J300含有作为抗肿瘤物质的由式(1)表示的5,3-二羟基-1-N-甲基 - 二氢吲哚-2-羰基氨基 - 丙氨酰 - 羟基异丁烯基 - 甘氨酸或其衍生物。 一种抗肿瘤药物组合物包含5,3-二羟基-1-N-甲基 - 二氢吲哚-2-羰基氨基 - 丙氨酰 - 羟基异亮氨酰基甘氨酸或其衍生物之一,包括5α,6α-环氧 - (22E,24R) 8(14),22-二烯-3β,7α-二醇,5α,6α-环氧 - (22E,24R) - 麦角甾-8,22-二烯-3β,7α 式(3)的二醇,式(4)的麦角胺-4,6,8(14),22-四烯-3-酮和3β,5α-二羟基-6β-甲氧麦角甾-7,22 - 二烯(式(5))。

    가잠을 이용한 애매미유충눈꽃동충하초의 인공재배 방법
    12.
    发明公开
    가잠을 이용한 애매미유충눈꽃동충하초의 인공재배 방법 有权
    使用国内丝绸培养ISARIA SINCLAIRII的方法

    公开(公告)号:KR1020030012998A

    公开(公告)日:2003-02-14

    申请号:KR1020010047271

    申请日:2001-08-06

    CPC classification number: A61K36/068

    Abstract: PURPOSE: A method for culturing Isaria sinclairii is provided by inoculating Isaria sinclairii to the pupa or larva of a domestic silkworm, thereby mass producing Isaria sinclairii . CONSTITUTION: The method for culturing Isaria sinclairii using a domestic silkworm comprises the steps of: inoculating spores of Isaria sinclairii to the larva or pupa of a domestic silkworm by spraying the spores on the surface of the larva or the pupa; and forming a fruit body of Isaria sinclairii from the infected pupa, wherein the inoculation process is carried out by diluting the spores of Isaria sinclairii in water in the concentration of 106/ml to 108/ml, spraying the diluted solution on the surfaces of the larvae or pupae of the domestic silkworms aged 2 weeks, 3 weeks, 4 weeks and 5 weeks, and leaving them under 95% of humidity for 12 hours; the larvae or pupae of the domestic silkworms are stored at 20 deg. C or less prior to the inoculation; and the fruit body formation process is carried out under conditions of 15 to 25 deg. C and humidity of 95%.

    Abstract translation: 目的:通过将Isaria sinclairii接种到家蚕的蛹或幼虫来提供Isaria sinclairii的培养方法,从而大量生产Isaria sinclairii。 构成:使用家蚕培养伊蚊(Isaria sinclairii)的方法包括以下步骤:通过将孢子喷洒在幼虫或蛹的表面上,将Isaria sinclairii的孢子接种到家蚕的幼虫或蛹中; 并从感染的蛹中形成Isaria sinclairii的果实体,其中通过在浓度为106 / ml至108 / ml的水中稀释Isaria sinclairii的孢子进行接种过程,将稀释的溶液喷洒在 家蚕的幼虫或蛹2周,3周,4周和5周,并将其置于95%湿度下12小时; 家蚕的幼虫或蛹保存在20度。 C以下; 果实体形成处理在15〜25℃的条件下进行。 C和湿度95%。

    누에분말을 이용한 곤충기생균 배지 조제방법
    13.
    发明公开
    누에분말을 이용한 곤충기생균 배지 조제방법 有权
    通过使用丝光粉来制备致病真菌中药的制备方法

    公开(公告)号:KR1020020067367A

    公开(公告)日:2002-08-22

    申请号:KR1020010007899

    申请日:2001-02-16

    CPC classification number: C12N1/14

    Abstract: PURPOSE: Provided is a preparation method of a medium for Entomopathogenic fungi effectively and economically by using silkworm powder used as a hypoglycemic agent. The medium increases the growth rate of Entomopathogenic fungi. CONSTITUTION: The medium for Entomopathogenic fungi is characterized by dissolving 24g of silkworm powder in 1L of distilled water; sterilizing it at 121 deg.C for 15 minutes; filtering the sterilized solution with gauze and a sieve sequentially; adding 15g of agar the pure solution; sterilizing it; and pipetting 21mL of the solution into each petridish the solidifying them.

    Abstract translation: 目的:通过使用用作降血糖药的蚕粉,有效和经济地提供了一种用于昆虫病原真菌的培养基的制备方法。 培养基增加了真菌致病真菌的生长速度。 构成:昆虫病原真菌的特征是将24g蚕粉溶解在1L蒸馏水中; 在121℃下灭菌15分钟; 用纱布和筛子依次过滤灭菌液; 加入15g琼脂纯溶液; 消毒; 并将21mL的溶液移液到每个头皮中固化。

    가잠을이용한동충하초의인공재배방법
    14.
    发明授权
    가잠을이용한동충하초의인공재배방법 失效
    培养天竺葵的方法

    公开(公告)号:KR100187897B1

    公开(公告)日:1999-06-01

    申请号:KR1019960062054

    申请日:1996-12-05

    Abstract: 본 발명은 항암·면역증강 등 각종 효능이 뛰어난 것으로 알려져 있으나 자연에서의 채집이 극히 어려운 관계로 인간에게 유용하게 이용되지 못하고 있는 동충하초(Paecilomyces japonica)를 인공재배하는 방법에 관한 것으로, 동충하초의 일종인 페실로마이세스 자포니카균 포자를 분무기를 이용하여 가잠의 4∼5령기 유충 또는 번데기 표피에 경피 접종한 후, 균사체를 형성한 번데기에서 자실체를 형성시키는 것을 특징으로 한다.

    가잠을 이용한 번데기동충하초의 인공재배 방법
    16.
    发明公开
    가잠을 이용한 번데기동충하초의 인공재배 방법 有权
    蚕蛹虫草的人工栽培方法

    公开(公告)号:KR1019980025198A

    公开(公告)日:1998-07-06

    申请号:KR1019970065095

    申请日:1997-12-01

    Abstract: 본 발명은 항암·면역증강 등 각종 효능이 뛰어난 것으로 알려져 있으나, 자연에서의 채집이 극히 어려운 관계로 인간에게 유용하게 이용되지 못하고 있는 동충하초(Cordyceps militaris)를 인공재배하는 방법에 관한 것으로, 동충하초의 일종인 코디셉스 밀리타리스의 포자를 가잠의 5령기 유충 표피에 분무 접종한 후, 균사체를 형성한 번데기에서 자실체를 형성시키는 것을 특징으로 한다.

    가잠을 이용한 애매미유충눈꽃동충하초의 인공재배 방법
    18.
    发明授权
    가잠을 이용한 애매미유충눈꽃동충하초의 인공재배 방법 有权
    가잠을이용한애매미유충눈꽃동충하초의인공재배방

    公开(公告)号:KR100407072B1

    公开(公告)日:2003-11-28

    申请号:KR1020010047271

    申请日:2001-08-06

    Abstract: PURPOSE: A method for culturing Isaria sinclairii is provided by inoculating Isaria sinclairii to the pupa or larva of a domestic silkworm, thereby mass producing Isaria sinclairii . CONSTITUTION: The method for culturing Isaria sinclairii using a domestic silkworm comprises the steps of: inoculating spores of Isaria sinclairii to the larva or pupa of a domestic silkworm by spraying the spores on the surface of the larva or the pupa; and forming a fruit body of Isaria sinclairii from the infected pupa, wherein the inoculation process is carried out by diluting the spores of Isaria sinclairii in water in the concentration of 106/ml to 108/ml, spraying the diluted solution on the surfaces of the larvae or pupae of the domestic silkworms aged 2 weeks, 3 weeks, 4 weeks and 5 weeks, and leaving them under 95% of humidity for 12 hours; the larvae or pupae of the domestic silkworms are stored at 20 deg. C or less prior to the inoculation; and the fruit body formation process is carried out under conditions of 15 to 25 deg. C and humidity of 95%.

    Abstract translation: 目的:通过将Isaria sinclairii接种到家蚕的蛹或幼虫来提供Isaria sinclairii的培养方法,由此大量生产Isaria sinclairii。 组成:使用家蚕培养Isaria sinclairii的方法包括以下步骤:通过将孢子喷洒在幼虫或蛹表面上,将Isaria sinclairii的孢子接种到家蚕的幼虫或蛹中; 并从感染的蛹中形成Isaria sinclairii的果实体,其中接种过程通过将Isaria sinclairii的孢子以106 / ml的浓度稀释到10 8 / ml,将稀释的溶液喷雾到 2周,3周,4周和5周的家蚕的幼虫或蛹,并将其置于95%的湿度下12小时; 家蚕的幼虫或蛹储存在20℃。 接种前C或更少; 并且在15至25度的条件下进行子实体形成过程。 C和95%的湿度。

    J300동충하초로부터 분리 및 정제한3-[5-(메톡시-에틸)-3,6-디옥소-피페라진-2-일]-프로피온산, 이를 포함하는 항 HIV 활성을 갖는 약제학적 조성물,AIDS 치료제 및 AIDS 치료보조식품
    19.
    发明公开
    J300동충하초로부터 분리 및 정제한3-[5-(메톡시-에틸)-3,6-디옥소-피페라진-2-일]-프로피온산, 이를 포함하는 항 HIV 활성을 갖는 약제학적 조성물,AIDS 치료제 및 AIDS 치료보조식품 有权
    从J300 CORDYCEPS MILITARIS提取和纯化的3-(5-(甲氧基 - 乙基)-3,6-二氧代哌嗪-2-基)丙酸和具有抗HIV活性的药物组合物,TREATIN代理

    公开(公告)号:KR1020020078322A

    公开(公告)日:2002-10-18

    申请号:KR1020010018664

    申请日:2001-04-09

    Abstract: PURPOSE: Provided are 3-(5-(methoxy-ethyl)-3,6-dioxo-piperazine-2-yl)-propionic acid of the formula(1) extracted and purified from the J300 Cordyceps militaris, and a pharmaceutical composition having anti-HIV activity, an agent for treating AIDS and a supplementary food containing the same. CONSTITUTION: The 3-(5-(methoxy-ethyl)-3,6-dioxo-piperazine-2-yl)-propionic acid of the formula(1) is manufactured by the steps of: extracting Cordyceps militaris powders with water; performing HPLC with the extract using distilled water; isolating the distilled water fraction by HPLC using methanol; and isolating the methanol fraction by activated carbon chromatography to obtain J300 Cordyceps militaris water extract Dong1-2-4 having anti-HIV activity.

    Abstract translation: 目的:提供从J300冬虫夏草提取和纯化的式(1)的3-(5-(甲氧基 - 乙基)-3,6-二氧代 - 哌嗪-2-基) - 丙酸和具有 抗艾滋病毒活动,治疗艾滋病的药物和含有艾滋病毒的补充食品。 构成:式(1)的3-(5-(甲氧基 - 乙基)-3,6-二氧代 - 哌嗪-2-基) - 丙酸通过以下步骤制备:用水提取冬虫夏草粉末; 使用蒸馏水用提取物进行HPLC; 使用甲醇通过HPLC分离蒸馏水部分; 并通过活性炭色谱分离甲醇馏分,得到具有抗HIV活性的J300冬虫夏草水提取物Dong1-2-4。

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