inhibitor-(Endocrinology)-+-产品-+-宁波康贝生化有限公司

产品分类

暂无分类

网站公告

宁波康贝生化竭诚为您提供各类多肽，小分子抑制剂。（各种难肽的研发以及畅销多肽的技术转让） www.karebay.com 联系人：高雅林 18217049878 QQ：2578105091 本公司提供产品均为药物用中间体，不得直接用于人体

联系方式

请先登录或注册后查看

荣誉资质

暂未上传

友情链接

暂无链接

新闻中心

暂无新闻

站内搜索

首页 > 产品 > inhibitor-(Endocrinology)

inhibitor-(Endocrinology)

单价	1.00 / mg
销量	暂无
发货	浙江宁波市付款后3天内
库存	1000mg起订1mg
品牌	karebay biochem
纯度	粗品-98%
报告	ESI-MS&HPLC
过期	长期有效
更新	2014-12-18 14:13

详细信息

Aminoglutethimide	125-84-8	Aminoglutethimide is an aromatase inhibitor with an IC50 of 20 µM....
Anastrozole	120511-73-1	Anastrozole is a potent and selective aromatase inhibitor with an IC50 value of 15 nM....
Anastrozole	120511-73-1	Anastrozole is a potent and selective aromatase inhibitor with an IC50 value of 15 nM....
Anastrozole	120511-73-1	Anastrozole is a potent and selective aromatase inhibitor with an IC50 value of 15 nM....
Andarine (GTX-007)	401900-40-1	Andarine is a selective non-steroidal androgen receptor modulator (SARM) with a Ki of 4 nM....
AZD1981	802904-66-1	....
Bicalutamide	90357-06-5	Bicalutamide is a pure androgen receptor (AR) antagonist used in the treatment of prostate cancer and hirsutism....
Bicalutamide	90357-06-5	Bicalutamide is a pure androgen receptor (AR) antagonist used in the treatment of prostate cancer and hirsutism....
Bicalutamide	90357-06-5	Bicalutamide is a pure androgen receptor (AR) antagonist used in the treatment of prostate cancer and hirsutism....
BX471	217645-70-0	BX471 is a potent nonpeptide CC chemokine receptor-1 (CCR1) antagonist....
BX471	217645-70-0	BX471 is a potent nonpeptide CC chemokine receptor-1 (CCR1) antagonist....
Candesartan	139481-59-7	....
Candesartan	139481-59-7	....
Clomifene citrate	50-41-9	....
Ctep	871362-31-1	....
Ctep	871362-31-1	....
Ctep	871362-31-1	....
Eplerenone	107724-20-9	Eplerenone is a selective aldosterone receptor blocker....
Eplerenone	107724-20-9	Eplerenone is a selective aldosterone receptor blocker....
Exemestane	107868-30-4	....
Exemestane	107868-30-4	....
Exemestane	107868-30-4	....
Exemestane	107868-30-4	....
GSK2578215A	1285515-21-0	GSK2578215A is a potent and highly selective leucine-rich repeat kinase 2 (LRRK2) inhibitor....
GSK2578215A	1285515-21-0	GSK2578215A is a potent and highly selective leucine-rich repeat kinase 2 (LRRK2) inhibitor....
GW9508	885101-89-3	GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 100-fold selective against GPR120, stimulates insulin secretion in a glucose-sensitive manner [1]....
GW9508	885101-89-3	GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 100-fold selective against GPR120, stimulates insulin secretion in a glucose-sensitive manner [1]....
H2L5186303	139262-76-3	H2L5186303 is a potent nonselective lysophosphatidic acid 2 (LPA2) and LPA3 antagonist....
H2L5186303	139262-76-3	H2L5186303 is a potent nonselective lysophosphatidic acid 2 (LPA2) and LPA3 antagonist....
ICI 182,780	129453-61-8	....
ICI 182,780	129453-61-8	....
ICI 182,780	129453-61-8	....
JNJ-26481585	875320-29-9	JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor....
JNJ-26481585	875320-29-9	JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor....
JNJ-26481585	875320-29-9	JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor....
JNJ-26481585	875320-29-9	JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor....
JNJ-26481585	875320-29-9	JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor....
Letrozole	112809-51-5	Letrozole is a third generation potent and selective aromatase inhibitor....
MDV3100	915087-33-1	MDV3100 is an androgen receptor (AR) antagonist with an IC50 of 36 nM....
MDV3100	915087-33-1	MDV3100 is an androgen receptor (AR) antagonist with an IC50 of 36 nM....
Exemestane	107868-30-4	....
Exemestane	107868-30-4	....
Exemestane	107868-30-4	....
GSK2578215A	1285515-21-0	GSK2578215A is a potent and highly selective leucine-rich repeat kinase 2 (LRRK2) inhibitor....
GSK2578215A	1285515-21-0	GSK2578215A is a potent and highly selective leucine-rich repeat kinase 2 (LRRK2) inhibitor....
GW9508	885101-89-3	GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 100-fold selective against GPR120, stimulates insulin secretion in a glucose-sensitive manner [1]....
GW9508	885101-89-3	GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 100-fold selective against GPR120, stimulates insulin secretion in a glucose-sensitive manner [1]....
H2L5186303	139262-76-3	H2L5186303 is a potent nonselective lysophosphatidic acid 2 (LPA2) and LPA3 antagonist....
H2L5186303	139262-76-3	H2L5186303 is a potent nonselective lysophosphatidic acid 2 (LPA2) and LPA3 antagonist....
ICI 182,780	129453-61-8	....
ICI 182,780	129453-61-8	....
ICI 182,780	129453-61-8	....
JNJ-26481585	875320-29-9	JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor....
JNJ-26481585	875320-29-9	JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor....
JNJ-26481585	875320-29-9	JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor....
JNJ-26481585	875320-29-9	JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor....
JNJ-26481585	875320-29-9	JNJ-26481585 is a novel pan histone deacetylase (HDAC) inhibitor....
Letrozole	112809-51-5	Letrozole is a third generation potent and selective aromatase inhibitor....
MDV3100	915087-33-1	MDV3100 is an androgen receptor (AR) antagonist with an IC50 of 36 nM....
MDV3100	915087-33-1	MDV3100 is an androgen receptor (AR) antagonist with an IC50 of 36 nM....
MDV3100	915087-33-1	MDV3100 is an androgen receptor (AR) antagonist with an IC50 of 36 nM....
Mifepristone	84371-65-3	Mifepristone is a selective antagonist at progesterone (PR) and glucocorticoid (GR) receptors with IC50 values of 307 and 100 nM, respectively....
NS6180	353262-04-1	NS6180 is a novel class of KCa3.1 channel inhibitors....
NS6180	353262-04-1	NS6180 is a novel class of KCa3.1 channel inhibitors....
Ostarine	841205-47-8	Ostarine is a selective androgen receptor modulator (SARM) with Ki of 3.8 nM....
Ostarine	841205-47-8	Ostarine is a selective androgen receptor modulator (SARM) with Ki of 3.8 nM....
Ostarine	841205-47-8	Ostarine is a selective androgen receptor modulator (SARM) with Ki of 3.8 nM....
Ostarine	841205-47-8	Ostarine is a selective androgen receptor modulator (SARM) with Ki of 3.8 nM....
PD 123319 ditrifluoroacetate	130663-39-7	....
Raloxifene HCl	82640-04-8	Raloxifene HCl is a hydrochloride salt form of raloxifene which is an oral selective estrogen receptor modulator....
Raloxifene HCl	82640-04-8	Raloxifene HCl is a hydrochloride salt form of raloxifene which is an oral selective estrogen receptor modulator....
SCH 563705	473728-58-4	SCH 563705 is a potent CXCR2 and CXCR1 antagonist with Ki values of 1 and 3 nM, respectively....
SCH 563705	473728-58-4	SCH 563705 is a potent CXCR2 and CXCR1 antagonist with Ki values of 1 and 3 nM, respectively....
SCH 563705	473728-58-4	SCH 563705 is a potent CXCR2 and CXCR1 antagonist with Ki values of 1 and 3 nM, respectively....
SCH 563705	473728-58-4	SCH 563705 is a potent CXCR2 and CXCR1 antagonist with Ki values of 1 and 3 nM, respectively....
SYN-115	870070-55-6	SYN-115 is a selective and potent adenosine A(2A) receptor antagonist....
SYN-115	870070-55-6	SYN-115 is a selective and potent adenosine A(2A) receptor antagonist....
SYN-115	870070-55-6	SYN-115 is a selective and potent adenosine A(2A) receptor antagonist....
SYN-115	870070-55-6	SYN-115 is a selective and potent adenosine A(2A) receptor antagonist....
TAK438	1260141-27-2	....
Taltirelin	103300-74-9	Taltirelin is a thyrotropin-releasing hormone (TRH) analog....
Taltirelin	103300-74-9	Taltirelin is a thyrotropin-releasing hormone (TRH) analog....
Tamoxifen	54965-24-1	Tamoxifen is a tissue-selective estrogen receptor modulator (SERM)....
Toremifene Citrate	89778-27-8	Toremifene Citrate is an estrogen agonist/antagonist indicated for the treatment of metastatic breast cancer in postmenopausal women with estrogen-receptor positive or unknown tumors [1]....
Torin 1	1222998-36-8	....
Torin 1	1222998-36-8	....
Trilostane	13647-35-3	Trilostane is an inhibitor of 3 β-hydroxysteroid dehydrogenase with an IC50 value of 1 µM....
Trilostane	13647-35-3	Trilostane is an inhibitor of 3 β-hydroxysteroid dehydrogenase with an IC50 value of 1 µM....
Trilostane	13647-35-3	Trilostane is an inhibitor of 3 β-hydroxysteroid dehydrogenase with an IC50 value of 1 µM....

可以根据客户要求定制合成，并按要求分装，提供各项检测指标以确保产品质量。

联系电话18217049878；QQ：2578105091

更多详情可邮件至karebaybio2002@163.com

药物用中间体，不得直接用于人体，仅供科研使用

宁波康贝生化有限公司
加关注0

多肽，小分子抑制剂，生化试剂

宁波康贝生化有限公司 加关注0

多肽，小分子抑制剂，生化试剂

宁波康贝生化有限公司
加关注0