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2-Amino-7-azido-2-methylheptanoic acid

中文名称
——
中文别名
——
英文名称
2-Amino-7-azido-2-methylheptanoic acid
英文别名
2-amino-7-azido-2-methylheptanoic acid
2-Amino-7-azido-2-methylheptanoic acid化学式
CAS
——
化学式
C8H16N4O2
mdl
——
分子量
200.24
InChiKey
APWRKZGSVYZPFX-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.8
  • 重原子数:
    14
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    77.7
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • [EN] NOVEL RADIOLABELLED CXCR4-TARGETING COMPOUNDS FOR DIAGNOSIS AND THERAPY<br/>[FR] NOUVEAUX COMPOSÉS RADIOMARQUÉS DIAGNOSTIQUES ET THÉRAPEUTIQUES CIBLANT CXCR4
    申请人:PROVINCIAL HEALTH SERVICES AUTHORITY
    公开号:WO2020210919A1
    公开(公告)日:2020-10-22
    This application relates to compounds of Formula (I): [targeting peptide]-N(R1)-X1(R2)L1-[linker]-RX n1 (I). The targeting peptide is cyclo[L-Phe-L-Tyr-L-Lys(iPr)-D-Arg-L-2-Nal-Gly-D-Glu]-L-Lys(iPr). R1 is H or methyl. X1 is an optionally substituted C1-C15 hydrocarbon optionally comprising heteroatoms. R2 is C(O)OH or C(O)NH2. L1 is a linkage (thiolether, amide, maleimide-thiol, triazole). The linker has a net negative charge at physiological pH and is a linear or branched chain of 1-10 units of X2L2 and/or X2(L2)2, wherein: each X2 is, independently, an optionally substituted C1-C15 hydrocarbon optionally comprising heteroatoms; and each L2 is a linkage. The linker optionally further comprises an albumin binder bonded to an L2. Each RX is a radiolabelling group linked through a separate L2, selected from: a metal chelator; a prosthetic group containing trifluoroborate (BF3); or a prosthetic group containing a silicon-fluorine-acceptor moiety. The compounds may be useful for imaging CXCR4-expressing tissues or for treating CXCR4-associated diseases or conditions (e.g. cancer).
    这个应用涉及到Formula (I)的化合物:[靶向肽]-N(R1)-X1(R2)L1-[连接物]-RX n1 (I)。靶向肽是cyclo[L-Phe-L-Tyr-L-Lys(iPr)-D-Arg-L-2-Nal-Gly-D-Glu]-L-Lys(iPr)。R1是H或甲基。X1是一个可选择地取代的含有杂原子的C1-C15烃。R2是C(O)OH或C(O)NH2。L1是一个连接物(醚、酰胺、马来酰亚胺-醇、三唑)。连接物在生理pH下具有净负电荷,是由1-10个X2L2和/或X2(L2)2的线性或支链构成,其中:每个X2独立地是一个可选择地取代的含有杂原子的C1-C15烃;每个L2是一个连接物。连接物可选择地进一步包括与L2结合的白蛋白结合剂。每个RX是通过单独的L2连接的放射标记基团,选自:螯合剂;含三硼酸盐(BF3)的假体基团;或含-受体基团的假体基团。这些化合物可能对于成像CXCR4表达组织或治疗与CXCR4相关的疾病或症状(如癌症)有用。
  • [EN] RADIOLABELED BOMBESIN-DERIVED COMPOUNDS FOR IN VIVO IMAGING OF GASTRIN-RELEASING PEPTIDE RECEPTOR (GRPR) AND TREATMENT OF GRPR-RELATED DISORDERS<br/>[FR] COMPOSÉS RADIOMARQUÉS DÉRIVÉS DE LA BOMBÉSINE POUR L'IMAGERIE IN VIVO DU RÉCEPTEUR DU PEPTIDE LIBÉRANT DE LA GASTRINE (GRPR) ET TRAITEMENT DES TROUBLES LIÉS AU GRPR
    申请人:PROVINCIAL HEALTH SERVICES AUTHORITY
    公开号:WO2021068051A1
    公开(公告)日:2021-04-15
    There is provided bombesin-derived compounds of Formula Ia (RX-L-Xaa1-Gln-Trp-Ala-Val-Xaa2-His-Xaa3-ψ-Xaa4-NH2). RX comprises a radionuclide chelator or a trifluoroborate-containing prosthetic group. L is a linker. Xaa1 is D-Phe, Cpa (4-chlorophenylalanine), D-Cpa, Tpi (2,3,4,9-tetrahydro-1H-pyrido[3,4b]indol-3-carboxylic acid), D-Tpi, Nal (naphthylalanine), or D-Nal. Xaa2 is Gly, N-methyl-Gly or D-Ala. Xaa3 is Leu, Pro, D-Pro, or Phe. Xaa4 is Pro, Phe, Tac (thiazolidine-4-carboxylic acid), Nle (norleucine), 4-oxa-L-Pro (oxazolidine-4-carboxylic acid). The symbol ψ represents a reduced peptide bond between Xaa3 and Xaa4 in which ψ is CH2-N when Xaa4 is Pro, Tac or 4-oxa-L-Pro, or ψ is CH2N(R) when Xaa4 is Phe or Nle wherein R is H or C1-C5 linear or branched alkyl. There is also provided the use of such compounds as imaging agents or therapeutic agents.
    提供了Formula Ia(RX-L-Xaa1-Gln-Trp-Ala-Val-Xaa2-His-Xaa3-ψ-Xaa4-NH2)的波美斯因衍生物。RX包括放射性同位素螯合剂或三硼酸酯含基团。L是连接剂。Xaa1是D-Phe,Cpa(4-氯苯酸),D-Cpa,Tpi(2,3,4,9-四氢-1H-吡啶[3,4b]吲哚-3-羧酸),D-Tpi,Nal(酸)或D-Nal。Xaa2是Gly,N-甲基-Gly或D-Ala。Xaa3是Leu,Pro,D-Pro或Phe。Xaa4是Pro,Phe,Tac(噻唑啉-4-羧酸),Nle(正癸酸),4-氧代-L-Pro(噁唑啉-4-羧酸)。符号ψ代表Xaa3和Xaa4之间的还原肽键,其中当Xaa4为Pro,Tac或4-氧代-L-Pro时,ψ为CH2-N,或当Xaa4为Phe或Nle时,ψ为 N(R),其中R为H或C1-C5线性或支链烷基。还提供了将这些化合物用作成像剂或治疗剂的用途。
  • [EN] RADIOLABELED COMPOUNDS TARGETING THE PROSTATE-SPECIFIC MEMBRANE ANTIGEN<br/>[FR] COMPOSÉS RADIOMARQUÉS CIBLANT L'ANTIGÈNE MEMBRANAIRE SPÉCIFIQUE DE LA PROSTATE
    申请人:PROVINCIAL HEALTH SERVICES AUTHORITY
    公开号:WO2020252598A1
    公开(公告)日:2020-12-24
    A compound comprising a prostate specific membrane antigen (PSMA)-targeting moiety of the following formula or of a salt or a solvate thereof. R0 is O or S. Each of R1a, R1b and R1c may be –CO2H, –SO2H, –SO3H, –PO2H, or –PO3H2, for example. R2 may be methylene or a derivative thereof, propylene or a derivative thereof, or a derivative of ethylene, optionally substituted. R3 is a linker. When the PSMA-targeting moiety is linked to a radiolabeling group, the compound may be used as an imaging agent or therapeutic agent for PSMA-expressing diseases/conditions.
    一种化合物,包括以下结构式或其盐或溶剂化合物的前列腺特异性膜抗原(PSMA)靶向基团。R0为O或S。R1a、R1b和R1c中的每一个可以是-CO2H、-SO2H、-SO3H、-PO2H或-PO3H2,例如。R2可以是亚甲基或其衍生物丙烯基或其衍生物,或乙烯的衍生物,可选择性地取代。R3是一个连接基。当PSMA靶向基团与放射标记基团连接时,该化合物可用作PSMA表达疾病/病况的成像剂或治疗剂。
  • [EN] NOVEL CXCR4-TARGETING COMPOUNDS<br/>[FR] NOUVEAUX COMPOSÉS CIBLANT CXCR4
    申请人:PROVINCIAL HEALTH SERVICES AUTHORITY
    公开号:WO2022082312A1
    公开(公告)日:2022-04-28
    The present disclosure relates to peptidic compounds of Formula A, A-II, A-III, B, or C, or salt or solvate thereof, compositions thereof, and methods of use thereof. The compounds of the present disclosure are useful for targeting CXCR4 for purposes such as imaging and/or therapeutics.
    本公开涉及A,A-II,A-III,B或C的肽化合物,或其盐或溶剂,以及其组合物和使用方法。本公开的化合物可用于针对CXCR4进行成像和/或治疗等目的。
  • [EN] NOVEL RADIOLABELLED COMPOUNDS FOR DIAGNOSIS OR TREATMENT OF PROSTATE-SPECIFIC MEMBRANE ANTIGEN-EXPRESSING CANCER<br/>[FR] NOUVEAUX COMPOSÉS RADIOMARQUÉS POUR LE DIAGNOSTIC OU LE TRAITEMENT DU CANCER EXPRIMANT UN ANTIGÈNE MEMBRANAIRE SPÉCIFIQUE DE LA PROSTATE
    申请人:PROVINCIAL HEALTH SERVICES AUTHORITY
    公开号:WO2020210909A1
    公开(公告)日:2020-10-22
    This application relates to compounds of Formula I. R1a, R1b and R1c is –CO2H, –SO2H, –SO3H, –SO4H, –PO2H, –PO3H or –PO4H. R2 is a linker, e.g. butylene. R3 is a linkage, e.g.–O–, –S–, -S(O)-, S(O)2-, –NHC(O)–, –C(O)NH–, or 1,2,3-triazole. R4 is –(CH2)0-3CH(R7)(CH2)0-3– wherein R7 is -(CH2)5CH3 or certain aromatic fused-ring systems. R5 and R6 are hydrogen or methyl. Each Xaa1 (if present) is an amino acid. RX is a radiolabeling group, e.g.: a radiometal chelator optionally bound by a radiometal; an aryl substituted with a radioisotope; a prosthetic group containing a trifluoroborate; or a prosthetic group containing a silicon-fluorine-acceptor moiety. The compounds may be useful for imaging prostate-specific membrane antigen (PSMA)-expressing tissues or for treating PSMA-expressing diseases (e.g. cancer).
    本申请涉及公式I的化合物。R1a,R1b和R1c为-CO2H,-SO2H,-SO3H,-SO4H,-PO2H,-PO3H或-PO4H。R2是一个连接器,例如丁二烯。R3是一个连接,例如-O-,-S-,-S(O)-,S(O)2-,-NHC(O)-,-C(O)NH-或1,2,3-三唑。R4是-(CH2)0-3CH(R7)( )0-3-,其中R7是-( )5CH3或特定的芳香融合环系统。R5和R6是氢或甲基。每个Xaa1(如果存在)都是一种氨基酸。RX是一个放射性标记基团,例如:放射性属螯合物,可选择地由放射性属结合;芳基取代的放射性同位素;含三硼酸盐的辅助基团;或含受体基团的辅助基团。这些化合物可能有用于成像前列腺特异性膜抗原(PSMA)表达组织或治疗PSMA表达疾病(例如癌症)。
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同类化合物

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