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ALLATOTROPIN

CAS No.
120928-88-3
Chemical Name:
ALLATOTROPIN
Synonyms
MAS-AT;ALLATOTROPIN;Allatotropin【Manduca sexta】;ALLATOTROPIN (1-13) (MANDUCA SEXTA);GFKNVEMMTARGF-NH2 (DISULFIDE BRIDGE: 2-7);GLY-PHE-LYS-ASN-VAL-GLU-MET-MET-THR-ALA-ARG-GLY-PHE-NH2;H-GLY-PHE-LYS-ASN-VAL-GLU-MET-MET-THR-ALA-ARG-GLY-PHE-NH2;Allatotropin H-Gly-Phe-Lys-Asn-Val-Glu-Met-Met-Thr-Ala-Arg-Gly-Phe-NH2;Gly-L-Phe-L-Lys-L-Asn-L-Val-L-Glu-L-Met-L-Met-L-Thr-L-Ala-L-Arg-Gly-L-Phe-NH2;H-GLY-PHE-LYS-ASN-VAL-GLU-MET-MET-THR-ALA-ARG-GLY-PHE-NH2 (DISULFIDE BRIDGE: 2-7)
CBNumber:
CB4103169
Molecular Formula:
C65H103N19O17S2
Molecular Weight:
1486.76
MDL Number:
MFCD00133060
MOL File:
120928-88-3.mol
Last updated:2025-06-18 16:39:18

ALLATOTROPIN Properties

storage temp. -15°C
Sequence Gly-Phe-Lys-Asn-Val-Glu-Met-Met-Thr-Ala-Arg-Gly-Phe-NH2

ALLATOTROPIN price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth FA108341 Allatotropin 120928-88-3 5mg $900 2026-06-04 Buy
Biosynth FA108341 Allatotropin 120928-88-3 2mg $900 2026-06-04 Buy
Biosynth FA108341 Allatotropin 120928-88-3 1mg $900 2026-06-04 Buy
Biosynth FA108341 Allatotropin 120928-88-3 10mg $1207.4 2026-06-04 Buy
Biosynth FA108341 Allatotropin 120928-88-3 25mg $2626.5 2026-06-04 Buy
Product number Packaging Price Buy
FA108341 5mg $900 Buy
FA108341 2mg $900 Buy
FA108341 1mg $900 Buy
FA108341 10mg $1207.4 Buy
FA108341 25mg $2626.5 Buy

ALLATOTROPIN Chemical Properties, Uses, Production

Description

Allatotropin is a pleiotropic peptide found in various invertebrates that shows myoregulatory activity. The name derives from its activity in regulating juvenile hormone biosynthesis by corpora allata in insects.

Structure

M. sexta allatotropin (Manse-AT) is a tridecapeptide with its C-terminal amidation. The family of this peptides, either isolated or predicted from cDNA sequences and transcriptomic data, have a similar sequence length (13–16 aa residues) and an amidated C-terminus.

Gene, mRNA, and precursor

Three alternatively spliced mRNAs for Manse-AT have been characterized.3 Each mRNA encodes a precursor protein, from which one copy of Manse-AT is derived. The two longer mRNAs contain the insertion of one or two alternative exons, each of which codes for one or two additional peptides structurally related to Manse- AT (Manse-ATL (AT-like) -I, -II, -III). A cDNA coding for a precursor protein containing Manse-AT and a peptide similar to Manse-ATL-III have been reported in other Lepidoptera, suggesting that the presence of the ATL peptide in addition to AT is not limited to M. sexta.

Biological function

Manse-AT stimulates JH biosynthesis by adult female CA from many lepidopteran insects, and larval CA from some lepidopteran species.Manse-AT is also reported to stimulate the CA of nonlepidopteran insects, such as the honey bee and blow fly, although no allatotropic peptide has been isolated from these insects.The expression of ATR in the CA observed in some insects readily explains the action of AT on the CA, but its expression in the CC rather than the CA in B. mori does not. In this species, because the ATR-expressing cells in the CC produce short neuropeptide-F (sNPF) and this peptide inhibits the JH synthetic activity of the CA in vitro, it is proposed that ATR may indirectly mediate AT activity on the CA by suppressing sNPF action on the CA.Besides the action on the CA, AT accelerates the heart rate, inhibits ion transport across the midgut epithelium, and controls the release of digestive enzymes in the midgut as well as muscle contraction, eventually affecting feeding behavior.10AT family peptides from hemimetabolous insects such as locust myotropin also show cardiostimulatory and myoregulatory activities.The effects of AT on noninsect invertebrates have been examined using synthetic mosquito AT. This AT showed myoregulatory activity on the turbellarians and hydra.A widespread role of AT in myoregulation and the presence of AT in organisms that do not have JH suggest that the primary role of AT is myoregulation and that the control of JH synthesis is secondary.

Uses

Allatotropin (Manse-AT) is a 13 amino acid neuropeptide. Allatotropin activates inositol 1,4,5-trisphosphate (IP3) pathway, and the biosynthesis of juvenile hormone (JH) in Manduca sexta[1].

References

[1] Reagan J D, et al., Allatotropin‐induced formation of inositol phosphates in the corpora allata of the moth, Manduca sexta[J]. Archives of insect biochemistry and physiology, 1992, 20(2): 145-155.

ALLATOTROPIN Preparation Products And Raw materials

Raw materials

Preparation Products

ALLATOTROPIN Suppliers

Global Suppliers ( 54)
Supplier Tel Email Country ProdList Advantage
GL Biochem (Shanghai) Ltd 21-61263452 13641803416 ymbetter@glbiochem.com China 9981 64
Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696 info@hanhongsci.com China 42917 64
Chemsky (shanghai) International Co.,Ltd 021-50135380 shchemsky@sina.com China 15350 60
Beijing Solarbio Science & Tecnology Co., Ltd. 17801761073 18101056239 3193328036@qq.com China 28150 68
Nanjing Peptide Biotech Ltd. 025-58361106-805 15951641583 zhao.xu@njpeptide.com China 9976 55
Chengdu Youngshe Chemical Co., Ltd. +86-17380623303 Caroline@youngshechem.com China 4724 58
Hangzhou Peptidego Biotech Co.,Ltd. 0571-87213919 15967184799 Eric@peptidego.com China 7872 58
Nanjing Meihao Pharmaceutical Technology Co., Ltd. meitaochem@126.com meitaochem@126.com China 19087 58
Hangzhou Go Top Peptide Biotech 0571-88211921 sales1@gotopbio.com CHINA 2609 58
Nanchang Tianzhen Biotechnology Co., Ltd 13758194781 13173652190 522013271@qq.com China 2447 58

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120928-88-3 (ALLATOTROPIN) Related Search:

MAS-AT H-GLY-PHE-LYS-ASN-VAL-GLU-MET-MET-THR-ALA-ARG-GLY-PHE-NH2 H-GLY-PHE-LYS-ASN-VAL-GLU-MET-MET-THR-ALA-ARG-GLY-PHE-NH2 (DISULFIDE BRIDGE: 2-7) GLY-PHE-LYS-ASN-VAL-GLU-MET-MET-THR-ALA-ARG-GLY-PHE-NH2 GFKNVEMMTARGF-NH2 (DISULFIDE BRIDGE: 2-7) ALLATOTROPIN ALLATOTROPIN (1-13) (MANDUCA SEXTA) Allatotropin【Manduca sexta】 Gly-L-Phe-L-Lys-L-Asn-L-Val-L-Glu-L-Met-L-Met-L-Thr-L-Ala-L-Arg-Gly-L-Phe-NH2 Allatotropin H-Gly-Phe-Lys-Asn-Val-Glu-Met-Met-Thr-Ala-Arg-Gly-Phe-NH2 L-Phenylalaninamide, glycyl-L-phenylalanyl-L-lysyl-L-asparaginyl-L-valyl-L-α-glutamyl-L-methionyl-L-methionyl-L-threonyl-L-alanyl-L-arginylglycyl- 120928-88-3 C65H103N19O17S2