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6918-09-8 分子结构
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N-(1-{2-[(carbamoylmethyl)carbamoyl]pyrrolidin-1-yl}-5-[(diaminomethylidene)amino]-1-oxopentan-2-yl)-2-{2-[2-(3-hydroxy-2-{2-[3-(1H-imidazol-5-yl)-2-[(5-oxopyrrolidin-2-yl)formamido]propanamido]-3-(1H-indol-3-yl)propanamido}propanamido)-3-(4-hydroxyphenyl)propanamido]acetamido}-4-methylpentanamide

ChemBase编号:526
分子式:C55H75N17O13
平均质量:1182.2901
单一同位素质量:1181.57302555
SMILES和InChIs

SMILES:
O=C(N1C(CCC1)C(=O)NCC(=O)N)C(NC(=O)C(NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C(NC(=O)C1NC(=O)CC1)Cc1[nH]cnc1)Cc1c2c([nH]c1)cccc2)CO)Cc1ccc(O)cc1)CC(C)C)CCCN=C(N)N
Canonical SMILES:
OCC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)N1CCCC1C(=O)NCC(=O)N)CCCN=C(N)N)CC(C)C)Cc1ccc(cc1)O)NC(=O)C(Cc1c[nH]c2c1cccc2)NC(=O)C(NC(=O)C1CCC(=O)N1)Cc1[nH]cnc1
InChI:
InChI=1S/C55H75N17O13/c1-29(2)19-38(49(80)67-37(9-5-17-60-55(57)58)54(85)72-18-6-10-43(72)53(84)62-25-44(56)75)66-46(77)26-63-47(78)39(20-30-11-13-33(74)14-12-30)68-52(83)42(27-73)71-50(81)40(21-31-23-61-35-8-4-3-7-34(31)35)69-51(82)41(22-32-24-59-28-64-32)70-48(79)36-15-16-45(76)65-36/h3-4,7-8,11-14,23-24,28-29,36-43,61,73-74H,5-6,9-10,15-22,25-27H2,1-2H3,(H2,56,75)(H,59,64)(H,62,84)(H,63,78)(H,65,76)(H,66,77)(H,67,80)(H,68,83)(H,69,82)(H,70,79)(H,71,81)(H4,57,58,60)
InChIKey:
XLXSAKCOAKORKW-UHFFFAOYSA-N

引用这个纪录

CBID:526 http://www.chembase.cn/molecule-526.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
N-(1-{2-[(carbamoylmethyl)carbamoyl]pyrrolidin-1-yl}-5-[(diaminomethylidene)amino]-1-oxopentan-2-yl)-2-{2-[2-(3-hydroxy-2-{2-[3-(1H-imidazol-5-yl)-2-[(5-oxopyrrolidin-2-yl)formamido]propanamido]-3-(1H-indol-3-yl)propanamido}propanamido)-3-(4-hydroxyphenyl)propanamido]acetamido}-4-methylpentanamide
IUPAC传统名
gonadorelin
商标名
Dirigestran
Dirigestran Spofa
Factrel
Fertagyl
Gonadorelina [INN-Spanish]
Gonadorelinum [INN-Latin]
Gonadotropin releasing hormone
Gonadotropin-releasing factor
Gonadotropin-releasing hormone
Human LH-RH
Hypocrine
Luforan
Lutal
Lutamin
Lutrefact
Lutrepulse
Lutrepulse KIT
Mammalian GnRH
Mammalian LH-RH
Ovine LH-RH
Porchine LH-RH
Porcine LH-releasing factor
Relefact
Relisorm
Relisorm L
Synthetic Gn-RH
Synthetic LH-FSH releasing hormone
Synthetic LH-RF
Synthetic LH-RH
Synthetic LH-releasing factor
Synthetic LH-releasing hormone
Synthetic LRF
Synthetic decapeptide FSH/LH-RH
Synthetic gonadoliberin
别名
Gonadorelin
CAS号
6918-09-8
PubChem SID
46506144
160963989
PubChem CID
36523

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
DrugBank DB00644 external link
PubChem 36523 external link
数据来源 数据ID 价格

理论计算性质

理论计算性质

JChem ALOGPS 2.1
里宾斯基五规则 false  Acid pKa 9.470687 
质子受体 17  质子供体 16 
LogD (pH = 5.5) -8.74699  LogD (pH = 7.4) -7.980599 
Log P -6.3192887  摩尔折射率 302.5053 cm3
极化性 117.86165 Å3 极化表面积 474.63 Å2
可自由旋转的化学键 31 
溶解度 5.88e-02 g/l  Log P -0.09 
LOG S -4.3 

分子性质

分子性质

理化性质 生物活性(PubChem)
溶解度
1 mg/mL expand 查看数据来源
疏水性(logP)
-3.6 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB00644 external link
Item Information
Drug Groups approved
Description Gonadorelin is another name for gonadotropin-releasing hormone (GnRH). It is a synthetic decapeptide prepared using solid phase peptide synthesis. GnRH is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary.
Indication For evaluating the functional capacity and response of the gonadotropes of the anterior pituitary also for evaluating residual gonadotropic function of the pituitary following removal of a pituitary tumor by surgery and/or irradiation.
Pharmacology Gonadorelin is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. In the pituitary GnRH stimulates synthesis and release of FSH and LH, a process that is controlled by the frequency and amplitude of GnRH pulses, as well as the feedback of androgens and estrogens. The pulsatility of GnRH secretion has been seen in all vertebrates, and it is necessary to ensure a correct reproductive function. Thus a single hormone, GnRH, controls a complex process of follicular growth, ovulation, and corpus luteum maintenance in the female, and spermatogenesis in the male. Its short half life requires infusion pumps for its clinical use
Toxicity LD50>3000 mg/kg (rat, oral)
Affected Organisms
Humans and other mammals
Biotransformation Rapidly hydrolyzed to inactive peptide components
Absorption Rapidly absorbed when injected
Half Life Very short, initial, 2 to 10 minutes; terminal, 10 to 40 minutes
References
Dungan HM, Clifton DK, Steiner RA: Minireview: kisspeptin neurons as central processors in the regulation of gonadotropin-releasing hormone secretion. Endocrinology. 2006 Mar;147(3):1154-8. Epub 2005 Dec 22. [Pubmed]
Franceschini I, Lomet D, Cateau M, Delsol G, Tillet Y, Caraty A: Kisspeptin immunoreactive cells of the ovine preoptic area and arcuate nucleus co-express estrogen receptor alpha. Neurosci Lett. 2006 Jul 3;401(3):225-30. Epub 2006 Apr 18. [Pubmed]
External Links
Wikipedia
RxList
Drugs.com

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Dungan HM, Clifton DK, Steiner RA: Minireview: kisspeptin neurons as central processors in the regulation of gonadotropin-releasing hormone secretion. Endocrinology. 2006 Mar;147(3):1154-8. Epub 2005 Dec 22. Pubmed
  • Franceschini I, Lomet D, Cateau M, Delsol G, Tillet Y, Caraty A: Kisspeptin immunoreactive cells of the ovine preoptic area and arcuate nucleus co-express estrogen receptor alpha. Neurosci Lett. 2006 Jul 3;401(3):225-30. Epub 2006 Apr 18. Pubmed
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专利

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